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REVIEW article

Front. Aging Neurosci., 08 August 2018
Sec. Neuroinflammation and Neuropathy
This article is part of the Research Topic Neuroinflammation and Cognition View all 16 articles

Interplay Between Age and Neuroinflammation in Multiple Sclerosis: Effects on Motor and Cognitive Functions

\r\nAlessandra Musella,Alessandra Musella1,2Antonietta Gentile,Antonietta Gentile3,4Francesca Romana RizzoFrancesca Romana Rizzo3Francesca De Vito,Francesca De Vito1,3Diego Fresegna,Diego Fresegna1,3Silvia Bullitta,Silvia Bullitta1,3Valentina Vanni,Valentina Vanni1,3Livia GuadalupiLivia Guadalupi1Mario Stampanoni BassiMario Stampanoni Bassi4Fabio ButtariFabio Buttari4Diego Centonze,*Diego Centonze3,4*Georgia Mandolesi,Georgia Mandolesi1,2
  • 1Laboratory of Synaptic Immunopathology, IRCCS San Raffaele Pisana, Rome, Italy
  • 2San Raffaele University of Rome, Rome, Italy
  • 3Laboratory of Synaptic Immunopathology, Department of Systems Medicine, University of Rome Tor Vergata, Rome, Italy
  • 4Unit of Neurology, Istituto Neurologico Mediterraneo (IRCCS Neuromed), Pozzilli, Italy

Aging is one of the main risk factors for the development of many neurodegenerative diseases. Emerging evidence has acknowledged neuroinflammation as potential trigger of the functional changes occurring during normal and pathological aging. Two main determinants have been recognized to cogently contribute to neuroinflammation in the aging brain, i.e., the systemic chronic low-grade inflammation and the decline in the regulation of adaptive and innate immune systems (immunosenescence, ISC). The persistence of the inflammatory status in the brain in turn may cause synaptopathy and synaptic plasticity impairments that underlie both motor and cognitive dysfunctions. Interestingly, such inflammation-dependent synaptic dysfunctions have been recently involved in the pathophysiology of multiple sclerosis (MS). MS is an autoimmune neurodegenerative disease, typically affecting young adults that cause an early and progressive deterioration of both cognitive and motor functions. Of note, recent controlled studies have clearly shown that age at onset modifies prognosis and exerts a significant effect on presenting phenotype, suggesting that aging is a significant factor associated to the clinical course of MS. Moreover, some lines of evidence point to the different impact of age on motor disability and cognitive deficits, being the former most affected than the latter. The precise contribution of aging-related factors to MS neurological disability and the underlying molecular and cellular mechanisms are still unclear. In the present review article, we first emphasize the importance of the neuroinflammatory dependent mechanisms, such as synaptopathy and synaptic plasticity impairments, suggesting their potential exacerbation or acceleration with advancing age in the MS disease. Lastly, we provide an overview of clinical and experimental studies highlighting the different impact of age on motor disability and cognitive decline in MS, raising challenging questions on the putative age-related mechanisms involved.

Introduction

Multiple sclerosis (MS) is an inflammatory neurodegenerative disease of the central nervous system (CNS), mainly affecting young adults. Its exact etiology remains unknown, but it is widely accepted that genetically susceptible individuals develop MS after exposure to undefined environmental triggers. MS is primarily characterized by a breakdown in immune tolerance to myelin and neuronal antigens and by a dysfunction of the blood brain barrier (Gourraud et al., 2012; Beecham et al., 2013; Olsson et al., 2017). Typically, infiltrating myelin-reactive lymphocytes (mainly T-cells but also B-cells) attack myelin sheaths and axon antigens on oligodendrocytes and neurons in the CNS. This event causes an inflammatory cascade, formation of large demyelinating plaques in the white matter and gliosis, neuroaxonal degeneration and synaptopathy, leading to an impairment of the neuronal signaling and, later on, to neurodegeneration (Compston and Coles, 2008; Dendrou et al., 2015; Mandolesi et al., 2015). Clinical manifestations include motor impairments, sensory and visual disturbances, fatigue, pain, mood disturbances and cognitive deficits, in relation to the spatiotemporal dissemination of pathological lesion sites in the CNS (Dendrou et al., 2015). Most of MS patients start with a relapsing remitting phase (RRMS), which later develops into a secondary progressive phase (SPMS). In primary progressive MS (PPMS) patients, the relapsing stage is absent and the disease starts already with a progressive loss of neurological functions (Compston and Coles, 2008; Disanto et al., 2010; Lassmann et al., 2012). Innate reparative processes can occur through remyelinating and neuronal repairing processes, which are highly variable among patients (Stangel, 2008; Bramow et al., 2010).

An important feature of adult MS is chronological age, consisting in a defined age interval between the mid-twenties and late-thirties for disease onset and a time limit, after the fifth decade, when the disorder is rarely diagnosed (Polliack et al., 2001; Sanai et al., 2016). Mounting evidence suggests that prognosis of MS appears to be, at least to some extent, dependent of age and not markedly influenced by the initial, exacerbating-remitting or progressive disease course (Confavreux and Vukusic, 2006; Scalfari et al., 2011; Cossburn et al., 2012; Sanai et al., 2016; Roy et al., 2017; Ruano et al., 2017). Many age-related changes affecting the brain could collectively affect neuronal viability and vulnerability in MS: increased iron accumulation, oxidative stress followed by mitochondrial injury, decrease of trophic support from the peri-plaque environment, decline of remyelination, chronic, systemic low grade inflammation as well as a broad increase in the production of inflammatory molecules such as pro-inflammatory cytokines (“inflammaging”; Pizza et al., 2011; Dorszewska, 2013; Dendrou et al., 2015; Di Benedetto et al., 2017; Bolton and Smith, 2018). Although further efforts are necessary to better clarify this aspect, the present review highlights common inflammatory processes occurring in both aging and MS brain that might be critical for understanding why age is an important risk factor for MS disability (motor and cognitive) and progression.

Immune System Dysregulation in MS: The Impact of Aging

Key age-associated changes in the CNS are triggered by microglia, their impaired regulation (low-grade inflammation and inflammaging) and the inflammatory and oxidative stressful environment they build up. Immune challenges, such as infections, surgery, or traumatic brain injuries, result in greater susceptibility to memory impairments and altered synaptic plasticity during aging (Ojo et al., 2015; Cornejo and von Bernhardi, 2016; Matt and Johnson, 2016; Bettio et al., 2017; Di Benedetto et al., 2017). On the other hand, advanced age is associated with a phenomenon called immunosenescence (ISC) which refers to a weakening in integrity and efficiency of the adaptive and innate immune systems (Walford, 1969; Denkinger et al., 2015; Di Benedetto et al., 2017).

In past years, researchers have spent much effort to understand the impact of aging and ISC on adaptive immunity in MS and in its rodent model, experimental autoimmune encephalomyelitis (EAE). From these studies, which were primarily focused on the analysis of biomarkers of ISC at peripheral level (Bolton and Smith, 2018), emerged that a premature ISC might operate during the course of MS and of EAE (Bolton and Smith, 2018). The effects of a prematurely aged immune system and ISC on MS and EAE are still unknown, but emerging data justifies and encourages further investigation. ISC typically affects both adaptive and innate immune systems. The most relevant changes in the adaptive immunity are decreased peripheral naïve T cells and concomitant accumulation of late-stage differentiated memory T cells, with reduced antigen receptor repertoire diversity. This phenomenon results from age-related impairments in the hematopoietic stem cell compartment (which generates few T-cell precursors), and from thymic involution. An increase of circulating cytokines facilitates a systemic and chronic, low-grade, inflammatory state which is typical of aging (termed “inflammaging”). This systemic inflammation may promote neuroinflammation by modulating glial cells, leading to an increased risk for developing neurodegeneration and cognitive impairment (CIs) in healthy individuals (Pizza et al., 2011; von Bernhardi et al., 2015; Di Benedetto et al., 2017). In MS patients, the additional inflammation carried by peripheral immune cell infiltration and by CNS-resident immune cell activation may significantly accelerate the inexorable aging processes in the CNS, and as the resulting stress response is excessive for homeostasis to be properly preserved (Dendrou et al., 2015), prominent neurodegenerative processes progressively follow (Figure 1).

FIGURE 1
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Figure 1. Key neuroinflammatory processes occurring in the central nervous system (CNS) of multiple sclerosis (MS) patients influenced by aging. Immune cell infiltration from the periphery, mainly through the blood–brain barrier, is a prominent feature of early-stage MS (top panel). Peripheral innate and adaptive immune cells, along with activated CNS-resident microglia and astrocytes, promote demyelination, axonal injury and synaptopathy mainly through action of soluble inflammatory (IL-1β, Interleukin-1β; TNF, tumor necrosis factor; IFN-γ, interferon-γ; IL-17, interleukin-17) and neurotoxic mediators. Neuronal damage can be completely or partly resolved due to remyelination, resolution of inflammation and neuroprotective/reparative mechanisms (growth factors). Furthermore, additional mechanisms, from local synaptic plasticity to brain rewiring, intervene to functionally compensate synaptic loss (long-term potentiation, LTP). With advancing years, premature aging processes such as peripheral immunosenescence (ISC) and inflammaging may lead to age-related changes in the blood. Neuronal senescence and unusual microglia (primed) activation as well as astrogliosis (IL-1β; IL-6; TNF; granulocyte–macrophage colony-stimulating factor, GM-CSF; CC-chemokine ligand 2, CCL2) might contribute at exacerbating MS neuroinflammatory processes (synaptopathy, impaired synaptic plasticity, reduced production of brain derived neurotrophic factor (BDNF) and insuline-like growth factor (IGF-1)). Later on (bottom panel), immune cell infiltration wanes, perhaps due to adaptive immune cell exhaustion from chronic antigen exposure. However, chronic CNS-intrinsic inflammation, and other processes influenced by age (such as oxidative stress, mitochondrial injury, iron accumulation and excitotoxicity) might contribute at exacerbating early pathological processes leading to neurodegeneration. Further microglial recruitment and activation might be induced by interaction with astrocytes releasing CCL2 and GM-CSF as occur during aging. Astrocytes can prevent remyelination at sites of neuroaxonal injury by inhibiting progenitor cells from developing into mature oligodendrocyte cells (ODCs). RNS, reactive nitrogen species; ROS, reactive oxygen species.

Accumulating evidence suggests that an exacerbation of common neuropathological aspects of MS and of aging brain, such as synaptic dysfunction and loss (synaptopathy) and synaptic plasticity impairment (Di Filippo et al., 2008; Weiss et al., 2014; Mandolesi et al., 2015; Stampanoni Bassi et al., 2017), might contribute to explain why aging may impact on MS disability.

Inflammatory Synaptopathy and Synaptic Plasticity in MS/EAE and in Aging Brain

Synaptopathy

Synaptophaty refers to a progressive dysfunction and loss of the synaptic compartment of the CNS that is emerging as a pathophysiological feature of MS disease and of its mouse model EAE (Mandolesi et al., 2015; Henstridge et al., 2016). Along with demyelination and axonal damage, synaptopathy contributes to the neurodegenerative decline of the CNS starting since the early phase of the disease. In MS and EAE, neuroinflammation is responsible for an imbalance between the glutamatergic and GABAergic systems in the brain and spinal cord. During acute inflammatory attacks in MS and EAE, pro-inflammatory cytokines (such as tumor necrosis factor (TNF); interleukin-1β (IL-1β)), released from activated microglia and astroglia as well as from infiltrating lymphocytes, trigger a progressive increase of the glutamatergic transmission and an impairment of the GABAergic synaptic response, leading to uncontrolled excitability and possibly to neurodegeneration (Centonze et al., 2009; Rossi et al., 2011, 2012, 2014; Mandolesi et al., 2012, 2013, 2017a; Nisticò et al., 2013; Mori et al., 2014a). Synaptopathy has long-lasting effects (such as excitotoxic damage) that can give rise to motor and CIs. It is remarkable that traits of neuroinflammatory synaptopathy are evident also in normal aging brains (Viviani and Boraso, 2011; Barrientos et al., 2015; Bettio et al., 2017), strongly suggesting an exacerbation with age of pathological events occurring in MS (Figure 1). It has been indeed suggested that during aging, peripheral ISC and inflammaging may favor the activation of microglia cells, leading to loss of their neuroprotective functions, to neuronal dysfunctions and tissue damage (Henry et al., 2009; Norden and Godbout, 2013; Matt and Johnson, 2016). The over-production of pro-inflammatory mediators, such as IL-1β, interleukin-6 (IL-6) and TNF, disrupts the delicate balance needed for synaptic homeostasis by modulating ion channels and glutamate receptors (Viviani and Boraso, 2011). In particular, data mainly obtained in animal models suggest that IL-1β and TNF exacerbate or favor excitotoxicity by modulating the N-methyl-D-aspartate (NMDA) and α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptors in the aging brain, mimicking the alterations occurring in MS and EAE brains (Jasek and Griffith, 1998; Viviani et al., 2003, 2006; Stellwagen et al., 2005; Centonze et al., 2009; Viviani and Boraso, 2011; Grasselli et al., 2013). Inflammatory dependent glutamate excitotoxicity and reduced production of neurotrophic factors (brain derived neurotrophic factor, BDNF; insuline-like growth factor, IGF-1) may impact neuronal functions (Figure 1) in aging brain (von Bernhardi et al., 2010; Dorszewska, 2013; Di Benedetto et al., 2017).

Synaptic Plasticity

Compelling evidence suggests that during aging, neuroinflammation may contribute to impaired long-term potentiation (LTP), which has been classically regarded, together with long-term depression (LTD), as the substrate for learning and memory processes (Viviani and Boraso, 2011; Barrientos et al., 2015; Di Benedetto et al., 2017).

The aged brain seems to be remarkably sensitive to an immune challenge in the periphery due to an unusual hyperactivation of microglia cells that, in cooperation with impairments in key regulatory systems, causes a long lasting neuroinflammatory state and age-related neurobehavioral complications (Norden et al., 2015; Di Benedetto et al., 2017). Age-related cognitive decline following an immune challenge likely depends on an exaggerated inflammatory response. In particular it has been shown in rodents that the pro-inflammatory cytokines IL-1β can impair synaptic plasticity through activation of MAP-kinases JNK and p38 and/or inhibition of BDNF and Arc, essential mediators of hippocampal-dependent memory processes (Barrientos et al., 2015; Lynch, 2015). Furthermore, pro-inflammatory cytokines contribute to negatively influence hippocampal neurogenesis with detrimental consequences for synaptic plasticity phenomena. Therefore, by impairing microglial priming or blocking the excessive brain cytokine response (pharmacologically or through diet and voluntary exercise) it may be possible to effectively attenuate the harmful effects of an immune insult on memory processes, supporting the view that pro-inflammatory cytokines play a pivotal and direct role in inducing long-term memory and cognitive deficits in older individuals (Di Benedetto et al., 2017).

In both MS and EAE, recent studies have shown that inflammatory cytokines are involved in synaptic plasticity alterations. Hippocampal LTP deficits have been detected in EAE mice during the acute phase of the disease, in association with an increased microglial activation, elevated levels of IL-1β, and a selective reduction of NMDA receptors (Di Filippo et al., 2015; Mancini et al., 2017). In MS patients, studies based on transcranial magnetic stimulation (TMS), a non-invasive technique commonly used to detect motor cortex plasticity in humans (Lefaucheur, 2005; Rossini and Rossi, 2007; Ziemann et al., 2008), have shown that synaptic plasticity phenomena are impaired in the progressive forms of the disease, usually diagnosed in people in their 40s (Mori et al., 2013; Stampanoni Bassi et al., 2017). In these patients, that are proned to adaptive immune cell exhaustion form prolonged antigenic exposure, a chronic CNS-intrinsic inflammation and neurodegeneration are prominent, suggesting a concomitant occurrence of cerebral aging and the accumulation of structural brain deterioration (Figure 1). However, a second relevant aspect should be taken in consideration in MS patients. As in other pathological conditions, it is increasingly emerging that synaptic plasticity phenomena, besides having a physiological role in learning and memory processes, drive also important neuroreparative mechanisms (Malenka and Bear, 2004; Pelletier et al., 2009). During MS disease, in the event of an immunological attack, brain damage is eluded by mechanisms of neuroprotection and neurorepair (Weiss et al., 2014; Di Filippo et al., 2015). When these mechanisms eventually fail, an irreversible damage occurs with consequent neuronal denervation. It has been proposed that additional mechanisms, collectively known as brain plasticity, intervene to functionally compensate the deficit of synaptic inputs. The more appropriate synaptic mechanisms underlying brain plasticity and that depend also on the inflammatory milieu are LTP and LTD. In particular, LTP seems to be able to compensate neuronal damage bringing back excitability in synaptic injured neurons. Interestingly, it has been proposed that LTP enhancement might be secondary to alterations of the glutamatergic and GABAergic balance induced by the inflammatory milieu, suggesting that CNS inflammation in MS patients is able to subvert plasticity (Mori et al., 2011, 2012, 2014a; Weiss et al., 2014; Stampanoni Bassi et al., 2017). Furthermore, taking advantage of non-invasive TMS studies, specific brain plasticity alterations have been associated with different disease phenotypes (RR-MS; PP-MS), or phases (remitting, relapsing), indicating that plastic phenomena can modulate disability progression and the clinical manifestation of the disease (Weiss et al., 2014; Stampanoni Bassi et al., 2017).

Age Is a Risk Factor for MS: Motor Disability, Cognitive Decline and Psychiatric Symptoms

Motor Disability

Evidence exists that increasing age is a significant factor influencing the clinical course of MS. Indeed, age at onset modifies prognosis and exerts a significant effect on the presenting phenotype of this disease (Confavreux and Vukusic, 2006; Tremlett et al., 2006; Scalfari et al., 2011; Tedeholm et al., 2015). Clinical studies reported that a younger onset age was strongly associated with a slower rate of disability accumulation. As shown in an observational study on 1844 patients, aging negatively affects the prognosis in MS, independently of the type of the initial course of the disease, be it exacerbating-remitting or progressive (Confavreux and Vukusic, 2006). Clinical data from the London Ontario database highlight that onset age of patients with the relapsing form of MS strongly influences the time to conversion to secondary progression; compared to age 20, onset at age 40 and at age 50 doubled and tripled risks of developing SP respectively, compared to age 20 (Scalfari et al., 2011). A clinical study on 500 MS patients, grouped by cutoff in onset age, demonstrated that the severity of disabilities was increased during and after an age band of 30 years–35 years (Ramachandran et al., 2014). In agreement, it has been reported that a younger age (20 years–35 years) is correlated with a longer time to reach disability milestone compared with older patients (36 years–65 years; Trojano et al., 2002), confirming that age at onset predicts the disease course. All together these results are in agreement with previous evidence that neurological relapses have only a limited influence on the risk of entering secondary progressive phase and on the latency of entering progression (Confavreux et al., 2000; Scalfari et al., 2010, 2013).

Furthermore, age at onset strongly predicts the probability of a patient to evolve in a primary progressive form of the disease. Kis et al. (2008) reported that the majority (83%) of MS patients with late-onset MS had a primary progressive disease course, whereas the young-onset MS group (94%) developed a relapsing-remitting form. Accordingly, motor deficits were significantly more frequent in the late-onset MS than in patients with young-onset MS (90% vs. 67%; Kis et al., 2008). Similar results were obtained in a previous study on 957 patients with MS, since age at onset predicted the likelihood of developing a primary progressive form and, for RRMS patients, strongly determined the time to conversion to secondary progression (Stankoff et al., 2007).

The impact of aging on brain pathology was also supported by the observation that median age at the time of assigned disability is substantially similar between patients with different clinical course or symptomatology. Among primary progressive and RR-SP patients, median ages at reaching a given disability score were strikingly similar (Scalfari et al., 2011), suggesting that age at onset has a strong impact on the neurodegenerative component of MS.

Cognitive Impairment

Together with motor disability, CI is frequently observed in MS patients (with an occurrence estimates between 40% and 65% of MS patients) and tends to progress over time. CI is present since the clinical onset of MS, more frequently in progressive patients compared to RRMS patients (Huijbregts et al., 2004; Ruet et al., 2013; Planche et al., 2016; Matias-Guiu et al., 2017), although heterogeneous results have been reported (Rao, 1991; Potagas et al., 2008).

In a 10-year longitudinal study, Amato et al. (2001) comparing cognitive capacities of 50 MS patients, found that cognitive dysfunction progressed as MS advances and that neurological and cognitive involvement tended to converge during the follow-up. The percentage of cognitive preserved patients decreased from 74% to 51% during 4 years of follow-up, and to 44% after 10-year assessment. In parallel, at the end of the study about 56% MS patients showed mild and moderate CI (Amato et al., 2001).

The relationship between CI, physical disability and age was further investigated in a larger study that compared prevalence and profile of cognitive deficit across 1040 patients with different clinical phenotypes (Ruano et al., 2017), including 167 clinically isolated syndrome, 759 RR, 74 SPMS and 40 PPMS patients. The multivariable analysis showed that higher disability (evaluated by EDSS) and older patient age, rather than clinical subtype and disease duration were the main determinant of CI. Furthermore, the study supported the evidence that the frequency of CI is increased in the progressive forms of the disease. Indeed, SP and PP patients showed approximately two-fold higher prevalence of CI when compared with RR and CIS patients.

The significant correlation with CI and age was reported also in two different Cross-Sectional studies. In the first study, 245 MS patients and 188 healthy control were evaluated using two measures of processing speed (the preliminary word reading and color naming trials of the Stroop) and the analysis were performed grouping participants into five age cohorts (Bodling et al., 2009).

In the second one, regression analyses were performed between age and several cognitive parameters (six outcomes T25FW, 9HPT, PASAT, SDMT, CVLT-II Learning and BVMT-R Learning) in 698 MS patients and 226 healthy subjects (Roy et al., 2017). Surprisingly in both clinical studies, although older MS patients were at higher risk of motor and cognitive disability, as expected, the interaction between MS and healthy control on cognitive test during lifespan was not significantly different, suggesting that age effects on CI are similar across healthy control and MS patients. Despite further longitudinal studies should be performed to determine and clarify the impact of aging on MS cognitive decline, these preliminary studies leave open interesting questions as discussed in the next paragraphs.

Psychiatric Symptoms

Recent studies have clearly demonstrated that also psychiatric affections are strongly associated with MS pathology. Depression and anxiety are known to be more prevalent among people with MS compared with the general population and individuals with other neurologic conditions (Boeschoten et al., 2017). Recently, several clinical (Imitola et al., 2005; Rossi et al., 2017) and preclinical studies (Haji et al., 2012; Gentile et al., 2016; Mandolesi et al., 2017b) have provided evidence that mood disturbances occur early in MS disease and its mouse model EAE and correlate with peripheral and central inflammation, independently of motor disability. Concerning the correlation between these psychological conditions and aging in MS, conflicting data are emerging. Several cross-sectional studies suggest that younger adults with MS are associated with greater risk for depressive symptoms respect to older patients (Patten et al., 2000, 2003; Chwastiak et al., 2002; Williams et al., 2005; Phillips and Stuifbergen, 2008). Accordingly, Kneebone et al. (2003) observed that older patients (70.6 ± 4.51 years) with MS were less affected by depressive symptoms with respect to younger patients (46.4 ± 8.35 years). Moreover, a significant correlation was found between the younger age at onset and the presence of depression in MS patients (Beiske et al., 2008). Interestingly, Williams et al. (2005) showed that a shorter duration of MS was associated with greater risk for depression. In contrast to these studies, da Silva et al. (2011) found that age was positively associated with depression in MS patients and Mattioli et al. (2011) reported that depressed MS patients were older than those not depressed (43.45 ± 12.15 years vs. 39.96 ± 10.88 years, p = 0.02). Finally, several cross-sectional studies on MS patients failed to replicate a relationship between depression and age (Galeazzi et al., 2005; Tsivgoulis et al., 2007; Bamer et al., 2008; Buchanan et al., 2009).

In conclusion, it is still not clear if aging may have an impact on MS psychiatric symptoms and further cross-sectional and longitudinal studies are needed to better investigate this challenging aspect, considering that a complex interplay of variables influences this form of comorbidity in MS (Boeschoten et al., 2017).

Collectively, these data support the hypothesis that in MS the shift from a predominantly inflammatory phase, dominated by clinical relapses, to a predominantly neurodegenerative phase, dominated by irreversible progression of neurological disability (motor and cognitive), may be mainly driven by biological factors related to aging (Lassmann et al., 2012; Friese et al., 2014; Mahad et al., 2015; Ruano et al., 2017; Zeydan and Kantarci, 2018).

Aging Reduces the Ability to Recover After a Relapse by Affecting Brain Plasticity

Several results concur with the hypothesis that the capacity of the brain to manage MS pathology depends on the ability to recover after a relapse. Of note, the ability to recover was strongly correlated to reserve of brain plasticity, which are diminished in older patients. A poor recovery of early relapses is indeed associated with an earlier progression of the pathology (Kalincik et al., 2014; Novotna et al., 2015). On the other hand, relapses with a higher impact and poorer recovery in MS patients were positively correlated with age (Kalincik et al., 2014) as well as a reduced ability to recover from initial relapse significantly declined with age (Cossburn et al., 2012). Aging has been indeed related to a decreased capability of functional reorganization and plasticity in MS, likely due to an interaction between cerebral aging and the accumulation of structural brain damage (Schoonheim et al., 2010).

It is now well recognized that MS-associated pathological processes progressively modify brain networks essential for functional domains such as sensorimotor function (Rocca et al., 2005; Tomassini et al., 2012), vision (Jenkins et al., 2010) and cognition (Rocca et al., 2015), by activating adaptive or maladaptive mechanisms. A form of adaptive plasticity can be considered the functional reorganization observed in the brain of MS patients in association to the easily performance of simple tasks; by means of this compensatory mechanism, more complex brain systems are recruited relatively to normal subjects (Pelletier et al., 2009). On the other hand, forms of maladaptive plasticity might also occur, causing functional changes directly linked to disability (Reddy et al., 2002). Functional MRI has contributed notably to improve our understanding of the mechanisms associated with preserved function in MS (Mainero et al., 2006; Filippi and Rocca, 2009; Rocca et al., 2010b, 2005; Enzinger et al., 2016). Thanks to these studies, it has been proposed that (Filippi and Rocca, 2009; Rocca et al., 2015) an increased involvement of the cortical networks might help at containing the functional impact of MS-related damage (Rocca et al., 2002a) and that changes in the organization of cortical areas involved in motor or cognitive tasks at different stages of the disease (Reddy et al., 2000a,b, 2002; Filippi et al., 2002a,b; Pantano et al., 2002; Rocca et al., 2002a,b, 2003a,b; Enzinger et al., 2016), might in part explain the discrepancy between brain injury and clinical disability. The progressive weakeaning of patterns of activation might account for progressive disability or CI in symptomatic MS patients, when compared to controls (Rocca et al., 2002b, 2010a; Ciccarelli et al., 2006) or asymptomatic MS patients (Penner et al., 2003; Mainero et al., 2006; Rocca et al., 2010a).

A deeper understanding of causal and functional relationships were achieved by neurophysiological techniques, predominantly by TMS (Zeller and Classen, 2014). Notably, accumulating evidence obtained through this technique have highlighted the ability of the brain to express LTP-like changes as a determinant factor to counteract disability progression in MS (Weiss et al., 2014; Stampanoni Bassi et al., 2017). Recently, it has been shown that a predictor of disease recovery from relapses is LTP induced by paired associative stimulation (Mori et al., 2014b). Furthermore, it has been observed that LTP induction in the primary motor cortex of patients in the early relapsing-remitting phases of the disease is possible and even enhanced. Conversely, LTP is absent in patients with a progressive form of MS (Mori et al., 2013; Weiss et al., 2014). Thus, it is conceivable that the capability of brain networks to adjust themselves in a plastic manner, allows a patient to accomplish with the focal and diffuse brain damage associated with the disease in the first years after MS onset. On the contrary, the disease likely enters in its more disabling progressive phase when the plastic reserve is exhausted. Accordingly, a study conducted on a cohort of RRMS patients with CI and on a group of cognitively preserved RRMS patients (Mori et al., 2011) revealed that LTP response was present only in the cognitively preserved group. Synaptic plasticity induction by PAS was also explored in RRMS and SPMS patients with stable clinical conditions in the last 3 months (Zeller et al., 2010), resulting in a comparable LTP amplitude between patients and gender, age-matched healthy controls. These observations suggest that alterations of synaptic plasticity emerge at the time of a relapse, as explored by other groups using paired associative stimulation (Mori et al., 2014b) or intermittent-theta burst stimulation (Mori et al., 2011).

Of note, LTP responses are variable among individuals and tend to decline with aging (Müller-Dahlhaus et al., 2008; Freitas et al., 2011). Accordingly, MS patients in their forties suffer from progressive forms during which LTP seems to be impaired. Current hypothesis to explain this inter-individual variability points to a combination of disease, age and likely genetic background (Pascual-Leone et al., 2011; Rossi et al., 2013) but further studies are necessary to clarify how population-level variability in LTP induction is related to MS disease phenotype and expression.

Does Aging Differentially Affect Motor and Cognitive Function in MS Patients?

We have summarized several data concurring with the hypothesis that the interaction between cerebral aging and overload of structural brain injury decreases plasticity and capability of functional reorganization in MS (Figure 1). However, unexpectedly, recent studies suggest that aging processes differentially affect motor and cognitive performances in patients with MS (Bodling et al., 2009; Roy et al., 2017). It seems that older MS patients are more susceptible to motor disability, and less to cognitive dysfunction. Although longitudinal studies, which should include both healthy controls and different MS subgroups, are demanded to better clarify this aspect, some speculations on this topic might be raised. Among different hypotheses, it has been suggested that in older MS patients, shorter axonal fibers are more prone to resilience and compensation than single long fibers that intervene in motor function. It might be also possible that a prominent and progressive damage of the spinal cord would also have a greater consequence on motor function over time. Furthermore, it is possible that a considerable effect on cognitive rather than motor abilities is played by the influence of cognitive reserve (CR) and personality traits (Sumowski et al., 2013; Roy et al., 2016). CR is indeed emerging as a second mechanism that might contribute at limiting cognitive deficits in MS patients (Rocca et al., 2018). Of note, the theory of CR emerged from aging and dementia studies to justify the inter-individual differences in the ability of managing with brain damage and the consequent cognitive deficits by means of pre-existing compensatory mechanisms (Stern, 2002). According to the CR theory, recent studies showed that intellectual enrichment (such as educational level, vocabulary knowledge, employment status), protects MS patients against the negative effect of disease-related damage on cognitive performance (Sumowski et al., 2009; Benedict et al., 2010; Ghaffar et al., 2012; Amato et al., 2013; Pinter et al., 2014; Rocca et al., 2018). In particular, it has been suggested that CR may have a protective role in preserving cognitive functions, mitigating the effect of structural damage on cognitive performance. However, in recent 2-years MS longitudinal study emerged that the CR protective role may diminish with disease progression.

Notably, it should be also taken in consideration that brain compensatory and adaptive mechanisms might depend on a genetic background. In this regard, recent evidence suggests that genetic determinants influence inter-individual differences in both MS severity and synaptic excitability (Rossi et al., 2013). In particular, four single nucleotide polymorphism (SNPs: rs4880213, rs6293, rs1805247, rs7301328) of the NMDAR genes were evaluated to search for associations with both synaptic excitability and disease outcome in RRMS and PPMS patients, considering that LTP is dependent on the synaptic activation of the glutamate NMDA receptor. This study showed that the specific T allele of the rs4880213 SNP of the NR1 subunit was correlated to an increase of neuronal excitability measured by means of paired TMS protocol. Furthermore, the same SNP was associated with better compensation of brain damage in RR-MS but with higher severity of PP-MS. Accordingly, these results supported the idea that potentiation of glutamatergic NMDAR-dependent synaptic transmission has a role in both adaptive plasticity and excitoxicity in MS patients. More interestingly, enhanced NMDAR function was found to preserve cognitive abilities in that cohort of patients, thus confirming the role played by NMDARs and NMDAR-dependent synaptic plasticity during learning and memory processes (Collingridge and Bliss, 1995; Nicoll and Malenka, 1999; Bennett, 2000; Cooke and Bliss, 2005, 2006). Notably, both RR-MS and PP-MS carrying the T allele of rs4880213 SNP showed a better performance at the Paced Auditory Serial Addition Test and the Symbol Digit Modalities Test, indicating residual NMDAR-dependent plasticity also in PP-MS. The above mentioned clinical tests explore cognitive domains frequently altered in MS, and impaired NMDAR-dependent synaptic plasticity in MS patients has been associated with poor performances at both tests (Mori et al., 2011). This evidence supports the idea that genetic determinants (SNPs) in combination with age and disease, might explain inter-individual variability of LTP responses (Pascual-Leone et al., 2011).

Although both genetic variability and CR could in part contribute to explain a potential less impact of age on cognitive decline, collectively these data clearly indicate that compensatory mechanisms of the brain can be potentially activated and responsive to therapeutic interventions even in PPMS patients (Feinstein et al., 2015). In this regard, despite some controversial results, it seems that increased physical activity is promising for cognitive benefits in MS (Dalgas and Stenager, 2012; Motl and Pilutti, 2012; Beier et al., 2014; Briken et al., 2014; Sandroff et al., 2014, 2016a; Motl et al., 2017). Indeed, in a randomized controlled trial of 42 patients with progressive MS (31 SPMS and 11 PPMS) with moderate physical disability (EDSS score 4–6), patients committed to several forms of exercise, rather than a wait list group, showed a significant amelioration in aerobic fitness and several secondary outcome measures, including cognitive performance (Briken et al., 2014). This study highlighted for the first time that physical activity specifically target cognition in patients with progressive MS but further studies are needed to identify the best type of exercise for cognitive recovery (Sandroff et al., 2016b; Motl et al., 2017; Ontaneda et al., 2017). Of note, in the aging context, it is emerging that exercise, as well as pharmacological treatments, may effectively block the detrimental effects of an immune challenge by preventing microglial priming or blocking the overstated brain cytokine response. This evidence not only suggests that these interventions may be useful therapeutic treatments, but also supports the view that a dysregulation of the fine interplay between the immune and nervous systems can have profound impacts on long-term plasticity and cognitive function in older individuals, as occurs in MS (Di Benedetto et al., 2017).

Conclusion

MS patients are indubitably exposed to the biological consequences of age, but the precise contribution of aging-related factors to MS neurological disability and the underlying molecular and cellular mechanisms are still unclear. Recent experimental and clinical investigations in the field of both aging and MS have shed a light onto common neuroinflammatory pathological mechanisms that are likely prematurely activated or exacerbated in MS patients, influencing the expression of the MS disease course. Here, we emphasize how a dysregulated synergy between the immune and nervous systems in the course of MS disease causes inflammation-dependent synaptic dysfunction, plasticity and degeneration with important implications on motor and cognitive functions. Since the early phase of MS, inflammatory dependent synaptopathy and synaptic plasticity perturbations seem to occur even independently of demyelination. As MS disease progresses, besides a decrease in remyelinating processes, brain repair and plasticity become exhausted while excitotoxic and neurodegenerative processes are exacerbated in association to a chronic CNS inflammation, supporting a late contribution of aging processes (Figure 2). Accordingly, cognitive dysfunction is now recognized to be an early symptoms of MS disease and for this reason it is included in diagnostic, follow-up and therapeutic evaluations (Nasios et al., 2018).

FIGURE 2
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Figure 2. Sequence of pathological and reparative events occurring during MS disease course, leading to severe neurological impairments. With advancing aging, neurodegenerative and neuroinflammatory processes are exacerbated causing severe cognitive and motor deficits. Inflammation is present at all stages of the disease, starting from an early phase dominated by peripheral immune cells invasion into the CNS to a progressive and chronic CNS inflammation. Since the early phase of the relapsing/remitting forms demyelination, synaptopathy and axonal damage occur causing progressive neurodegeneration. To avoid brain damage and to functionally compensate for eventual deficits of synaptic inputs, mechanisms of neuroprotection, remyelination and synaptic plasticity intervene. The transition from relapsing-remitting course MS (RRMS) to secondary progressive MS (SPMS) is likely to be the point at which the compensatory brain plasticity reserve bypassing of neuronal injury is exhausted. Usually after the fifth decade, regardless of the preceding disease course and severity, the inevitability and the rate of neurological decline are highly consistent.

Finally, we highlighted unexpected results obtained from clinical studies conducted on MS patients and healthy controls, revealing a milder effect of aging on MS cognitive function relative to motor disability. Although further investigations are necessary to clarify this aspect, it would be interesting to investigate also which compensatory mechanisms in MS brain are specifically involved. Considering the emerging view of a bidirectional communication between the nervous system and immune system, in which neuroinflammatory processes can be adaptive and beneficial (Schwartz and Deczkowska, 2016), it may be suggested that in the aging MS brains, a vicious interaction between the compromised immune and neuronal systems culminates in a protective and adaptive mechanisms of the neuro-immune system.

In conclusion, a more precise comprehension of the temporal (with age) and spatial distribution and activity of immune players in MS brain in association with specific stages of disease, genetic determinants and brain plasticity reserve is essential to determine the deep nature of the pathology, and thus the ideal strategy required to treat it.

Author Contributions

AM, DC and GM conceived and designed the manuscript. All the other authors made significant contributions, reviewed and approved the manuscript.

Funding

This work was supported by the Italian Ministry of Health (Ricerca corrente—IRCCS San Raffaele Pisana; Ricerca corrente—IRCCS Neuromed and 5 × 1,000 IRCCS Neuromed).

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We would like to acknowledge funding from Umberto Veronesi Foundation for fellowship to AG.

Abbreviations

AMPA, α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid; BDNF, brain derived neurotrophic factor; CI, cognitive impairment; CNS, central nervous system; CR, cognitive reserve; EAE, experimental autoimmune encephalomyelitis; GABA, γ-aminobutyric acid; IGF-1, insuline-like growth factor; IL-17, interleukin-17; IL-1β, Interleukin-1β; IL-6, Interleukin-6; ISC, immunosenescence; IFNγ, interferon-γ; LTD, long-term depression; LTP, long-term potentiation; MS, multiple sclerosis; NMDA, N-methyl-D-aspartate; PPMS, primary progressive MS; RNS, reactive nitrogen species; ROS, reactive oxygen species; RRMS, relapsing–remitting course; SNP, single nucleotide polymorphism; SPMS, secondary progressive MS; TMS, transcranial magnetic stimulation; TNF, tumor necrosis factor.

References

Amato, M. P., Ponziani, G., Siracusa, G., and Sorbi, S. (2001). Cognitive dysfunction in early-onset multiple sclerosis: a reappraisal after 10 years. Arch. Neurol. 58, 1602–1606. doi: 10.1001/archneur.58.10.1602

PubMed Abstract | CrossRef Full Text | Google Scholar

Amato, M. P., Razzolini, L., Goretti, B., Stromillo, M. L., Rossi, F., Giorgio, A., et al. (2013). Cognitive reserve and cortical atrophy in multiple sclerosis: a longitudinal study. Neurology 80, 1728–1733. doi: 10.1212/WNL.0b013e3182918c6f

PubMed Abstract | CrossRef Full Text | Google Scholar

Bamer, A. M., Cetin, K., Johnson, K. L., Gibbons, L. E., and Ehde, D. M. (2008). Validation study of prevalence and correlates of depressive symptomatology in multiple sclerosis. Gen. Hosp. Psychiatry 30, 311–317. doi: 10.1016/j.genhosppsych.2008.04.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Barrientos, R. M., Kitt, M. M., Watkins, L. R., and Maier, S. F. (2015). Neuroinflammation in the normal aging hippocampus. Neuroscience 309, 84–99. doi: 10.1016/j.neuroscience.2015.03.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Beecham, A. H., Patsopoulos, N. A., Xifara, D. K., Davis, M. F., Kemppinen, A., Cotsapas, C., et al. (2013). Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat. Genet. 45, 1353–1360. doi: 10.1038/ng.2770

PubMed Abstract | CrossRef Full Text | Google Scholar

Beier, M., Bombardier, C. H., Hartoonian, N., Motl, R. W., and Kraft, G. H. (2014). Improved physical fitness correlates with improved cognition in multiple sclerosis. Arch. Phys. Med. Rehabil. 95, 1328–1334. doi: 10.1016/j.apmr.2014.02.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Beiske, A. G., Svensson, E., Sandanger, I., Czujko, B., Pedersen, E. D., Aarseth, J. H., et al. (2008). Depression and anxiety amongst multiple sclerosis patients. Eur. J. Neurol. 15, 239–245. doi: 10.1111/j.1468-1331.2007.02041.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Benedict, R. H. B., Morrow, S. A., Weinstock Guttman, B., Cookfair, D., and Schretlen, D. J. (2010). Cognitive reserve moderates decline in information processing speed in multiple sclerosis patients. J. Int. Neuropsychol. Soc. 16, 829–835. doi: 10.1017/s1355617710000688

PubMed Abstract | CrossRef Full Text | Google Scholar

Bennett, M. R. (2000). The concept of long term potentiation of transmission at synapses. Prog. Neurobiol. 60, 109–137. doi: 10.1016/s0301-0082(99)00006-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Bettio, L. E. B., Rajendran, L., and Gil-Mohapel, J. (2017). The effects of aging in the hippocampus and cognitive decline. Neurosci. Biobehav. Rev. 79, 66–86. doi: 10.1016/j.neubiorev.2017.04.030

PubMed Abstract | CrossRef Full Text | Google Scholar

Bodling, A. M., Denney, D. R., and Lynch, S. G. (2009). Cognitive aging in patients with multiple sclerosis: a cross-sectional analysis of speeded processing. Arch. Clin. Neuropsychol. 24, 761–767. doi: 10.1093/arclin/acp076

PubMed Abstract | CrossRef Full Text | Google Scholar

Boeschoten, R. E., Braamse, A. M. J., Beekman, A. T. F., Cuijpers, P., van Oppen, P., Dekker, J., et al. (2017). Prevalence of depression and anxiety in Multiple Sclerosis: a systematic reviewand meta-analysis. J. Neurol. Sci. 372, 331–341. doi: 10.1016/j.jns.2016.11.067

PubMed Abstract | CrossRef Full Text | Google Scholar

Bolton, C., and Smith, P. A. (2018). The influence and impact of ageing and immunosenescence (ISC) on adaptive immunity during multiple sclerosis (MS) and the animal counterpart experimental autoimmune encephalomyelitis (EAE). Ageing Res. Rev. 41, 64–81. doi: 10.1016/j.arr.2017.10.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Bramow, S., Frischer, J. M., Lassmann, H., Koch-Henriksen, N., Lucchinetti, C. F., Sørensen, P. S., et al. (2010). Demyelination versus remyelination in progressive multiple sclerosis. Brain 133, 2983–2998. doi: 10.1093/brain/awq250

PubMed Abstract | CrossRef Full Text | Google Scholar

Briken, S., Gold, S. M., Patra, S., Vettorazzi, E., Harbs, D., Tallner, A., et al. (2014). Effects of exercise on fitness and cognition in progressive MS: a randomized, controlled pilot trial. Mult. Scler. J. 20, 382–390. doi: 10.1177/1352458513507358

PubMed Abstract | CrossRef Full Text | Google Scholar

Buchanan, R. J., Chakravorty, B. J., Tyry, T., Hatcher, W., and Vollmer, T. (2009). Age-related comparisons of people with multiple sclerosis: demographic, disease, and treatment characteristics. NeuroRehabilitation 25, 271–278. doi: 10.3233/NRE-2009-0525

PubMed Abstract | CrossRef Full Text | Google Scholar

Centonze, D., Muzio, L., Rossi, S., Cavasinni, F., De Chiara, V., Bergami, A., et al. (2009). Inflammation triggers synaptic alteration and degeneration in experimental autoimmune encephalomyelitis. J. Neurosci. 29, 3442–3452. doi: 10.1523/JNEUROSCI.5804-08.2009

PubMed Abstract | CrossRef Full Text | Google Scholar

Chwastiak, L., Ehde, D. M., Gibbons, L. E., Sullivan, M., Bowen, J. D., and Kraft, G. H. (2002). Depressive symptoms and severity of illness in multiple sclerosis: epidemiologic study of a large community sample. Am. J. Psychiatry 159, 1862–1868. doi: 10.1176/appi.ajp.159.11.1862

PubMed Abstract | CrossRef Full Text | Google Scholar

Ciccarelli, O., Toosy, A. T., Marsden, J. E., Wheeler-Kingshott, C. M., Miller, D. H., Matthews, P. M., et al. (2006). Functional response to active and passive ankle movements with clinical correlations in patients with primary progressive multiple sclerosis. J. Neurol. 253, 882–891. doi: 10.1007/s00415-006-0125-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Collingridge, G. L., and Bliss, T. V. P. (1995). Memories of NMDA receptors and LTP. Trends Neurosci. 18, 54–56. doi: 10.1016/0166-2236(95)80016-u

PubMed Abstract | CrossRef Full Text | Google Scholar

Compston, A., and Coles, A. (2008). Multiple sclerosis. Lancet 372, 1502–1517. doi: 10.1016/S0140-6736(08)61620-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Confavreux, C., and Vukusic, S. (2006). Age at disability milestones in multiple sclerosis. Brain 129, 595–605. doi: 10.1093/brain/awh714

PubMed Abstract | CrossRef Full Text | Google Scholar

Confavreux, C., Vukusic, S., Moreau, T., and Adeleine, P. (2000). Relapses and progression of disability in multiple sclerosis. N. Engl. J. Med. 343, 1430–1438. doi: 10.1056/nejm200011163432001

PubMed Abstract | CrossRef Full Text | Google Scholar

Cooke, S. F., and Bliss, T. V. P. (2005). Long-term potentiation and cognitive drug discovery. Curr. Opin. Investig. Drugs 6, 25–34.

PubMed Abstract | Google Scholar

Cooke, S. F., and Bliss, T. V. P. (2006). Plasticity in the human central nervous system. Brain 129, 1659–1673. doi: 10.1093/brain/awl082

PubMed Abstract | CrossRef Full Text | Google Scholar

Cornejo, F., and von Bernhardi, R. (2016). Age-dependent changes in the activation and regulation of microglia. Adv. Exp. Med. Biol. 949, 205–226. doi: 10.1007/978-3-319-40764-7_10

PubMed Abstract | CrossRef Full Text | Google Scholar

Cossburn, M., Ingram, G., Hirst, C., Ben-Shlomo, Y., Pickersgill, T. P., and Robertson, N. P. (2012). Age at onset as a determinant of presenting phenotype and initial relapse recovery in multiple sclerosis. Mult. Scler. J. 18, 45–54. doi: 10.1177/1352458511417479

PubMed Abstract | CrossRef Full Text | Google Scholar

da Silva, A. M., Vilhena, E., Lopes, A., Santos, E., Gonçalves, M. A., Pinto, C., et al. (2011). Depression and anxiety in a Portuguese MS population: associations with physical disability and severity of disease. J. Neurol. Sci. 306, 66–70. doi: 10.1016/j.jns.2011.03.042

PubMed Abstract | CrossRef Full Text | Google Scholar

Dalgas, U., and Stenager, E. (2012). Exercise and disease progression in multiple sclerosis: can exercise slow down the progression of multiple sclerosis? Ther. Adv. Neurol. Disord. 5, 81–95. doi: 10.1177/1756285611430719

PubMed Abstract | CrossRef Full Text | Google Scholar

Dendrou, C. A., Fugger, L., and Friese, M. A. (2015). Immunopathology of multiple sclerosis. Nat. Rev. Immunol. 15, 545–558. doi: 10.1038/nri3871

PubMed Abstract | CrossRef Full Text | Google Scholar

Denkinger, M. D., Leins, H., Schirmbeck, R., Florian, M. C., and Geiger, H. (2015). HSC aging and senescent immune remodeling. Trends Immunol. 36, 815–824. doi: 10.1016/j.it.2015.10.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Di Benedetto, S., Müller, L., Wenger, E., Düzel, S., and Pawelec, G. (2017). Contribution of neuroinflammation and immunity to brain aging and the mitigating effects of physical and cognitive interventions. Neurosci. Biobehav. Rev. 75, 114–128. doi: 10.1016/j.neubiorev.2017.01.044

PubMed Abstract | CrossRef Full Text | Google Scholar

Di Filippo, M., de Iure, A., Durante, V., Gaetani, L., Mancini, A., Sarchielli, P., et al. (2015). Synaptic plasticity and experimental autoimmune encephalomyelitis: implications for multiple sclerosis. Brain Res. 1621, 205–213. doi: 10.1016/j.brainres.2014.12.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Di Filippo, M., Sarchielli, P., Picconi, B., and Calabresi, P. (2008). Neuroinflammation and synaptic plasticity: theoretical basis for a novel, immune-centred, therapeutic approach to neurological disorders. Trends Pharmacol. Sci. 29, 402–412. doi: 10.1016/j.tips.2008.06.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Disanto, G., Berlanga, A. J., Handel, A. E., Para, A. E., Burrell, A. M., Fries, A., et al. (2010). Heterogeneity in multiple sclerosis: scratching the surface of a complex disease. Autoimmune Dis. 2011:932351. doi: 10.4061/2011/932351

PubMed Abstract | CrossRef Full Text | Google Scholar

Dorszewska, J. (2013). Cell biology of normal brain aging: synaptic plasticity-cell death. Aging Clin. Exp. Res. 25, 25–34. doi: 10.1007/s40520-013-0004-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Enzinger, C., Pinter, D., Rocca, M. A., De Luca, J., Sastre-Garriga, J., Audoin, B., et al. (2016). Longitudinal fMRI studies: exploring brain plasticity and repair in MS. Mult. Scler. 22, 269–278. doi: 10.1177/1352458515619781

PubMed Abstract | CrossRef Full Text | Google Scholar

Feinstein, A., Freeman, J., and Lo, A. C. (2015). Treatment of progressive multiple sclerosis: what works, what does not, and what is needed. Lancet Neurol. 14, 194–207. doi: 10.1016/s1474-4422(14)70231-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Filippi, M., and Rocca, M. A. (2009). Functional mr imaging in multiple sclerosis. Neuroimaging Clin. N. Am. 19, 59–70. doi: 10.1016/j.nic.2008.08.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Filippi, M., Rocca, M. A., Colombo, B., Falini, A., Codella, M., Scotti, G., et al. (2002a). Functional magnetic resonance imaging correlates of fatigue in multiple sclerosis. Neuroimage 15, 559–567. doi: 10.1006/nimg.2001.1011

PubMed Abstract | CrossRef Full Text | Google Scholar

Filippi, M., Rocca, M. A., Falini, A., Caputo, D., Ghezzi, A., Colombo, B., et al. (2002b). Correlations between structural CNS damage and functional MRI changes in primary progressive MS. Neuroimage 15, 537–546. doi: 10.1006/nimg.2001.1023

PubMed Abstract | CrossRef Full Text | Google Scholar

Freitas, C., Perez, J., Knobel, M., Tormos, J. M., Oberman, L., Eldaief, M., et al. (2011). Changes in cortical plasticity across the lifespan. Front. Aging Neurosci. 3:5. doi: 10.3389/fnagi.2011.00005

PubMed Abstract | CrossRef Full Text | Google Scholar

Friese, M. A., Schattling, B., and Fugger, L. (2014). Mechanisms of neurodegeneration and axonal dysfunction in multiple sclerosis. Nat. Rev. Neurol. 10, 225–238. doi: 10.1038/nrneurol.2014.37

PubMed Abstract | CrossRef Full Text | Google Scholar

Galeazzi, G. M., Ferrari, S., Giaroli, G., Mackinnon, A., Merelli, E., Motti, L., et al. (2005). Psychiatric disorders and depression in multiple sclerosis outpatients: impact of disability and interferon β therapy. Neurol. Sci. 26, 255–262. doi: 10.1007/s10072-005-0468-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Gentile, A., Fresegna, D., Musella, A., Sepman, H., Bullitta, S., De Vito, F., et al. (2016). Interaction between interleukin-1β and type-1 cannabinoid receptor is involved in anxiety-like behavior in experimental autoimmune encephalomyelitis. J. Neuroinflammation 13:231. doi: 10.1186/s12974-016-0682-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Ghaffar, O., Fiati, M., and Feinstein, A. (2012). Occupational attainment as a marker of cognitive reserve in multiple sclerosis. PLoS One 7:e47206. doi: 10.1371/journal.pone.0047206

PubMed Abstract | CrossRef Full Text | Google Scholar

Gourraud, P. A., Harbo, H. F., Hauser, S. L., and Baranzini, S. E. (2012). The genetics of multiple sclerosis: an up-to-date review. Immunol. Rev. 248, 87–103. doi: 10.1111/j.1600-065X.2012.01134.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Grasselli, G., Rossi, S., Musella, A., Gentile, A., Loizzo, S., Muzio, L., et al. (2013). Abnormal NMDA receptor function exacerbates experimental autoimmune encephalomyelitis. Br. J. Pharmacol. 168, 502–517. doi: 10.1111/j.1476-5381.2012.02178.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Haji, N., Mandolesi, G., Gentile, A., Sacchetti, L., Fresegna, D., Rossi, S., et al. (2012). TNF-α-mediatedanxiety in a mouse model of multiple sclerosis. Exp. Neurol. 237, 296–303. doi: 10.1016/j.expneurol.2012.07.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Henry, C. J., Huang, Y., Wynne, A. M., and Godbout, J. P. (2009). Peripheral lipopolysaccharide (LPS) challenge promotes microglial hyperactivity in aged mice that is associated with exaggerated induction of both pro-inflammatory IL-1β and anti-inflammatory IL-10 cytokines. Brain Behav. Immun. 23, 309–317. doi: 10.1016/j.bbi.2008.09.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Henstridge, C. M., Pickett, E., and Spires-Jones, T. L. (2016). Synaptic pathology: a shared mechanism in neurological disease. Ageing Res. Rev. 28, 72–84. doi: 10.1016/j.arr.2016.04.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Huijbregts, S. C. J., Kalkers, N. F., de Sonneville, L. M. J., de Groot, V., Reuling, I. E. W., and Polman, C. H. (2004). Differences in cognitive impairment of relapsing remitting, secondary, and primary progressive MS. Neurology 63, 335–339. doi: 10.1212/01.WNL.0000129828.03714.90

PubMed Abstract | CrossRef Full Text | Google Scholar

Imitola, J., Chitnis, T., and Khoury, S. J. (2005). Cytokines in multiple sclerosis: from bench to bedside. Pharmacol. Ther. 106, 163–177. doi: 10.1016/j.pharmthera.2004.11.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Jasek, M. C., and Griffith, W. H. (1998). Pharmacological characterization of ionotropic excitatory amino acid receptors in young and aged rat basal forebrain. Neuroscience 82, 1179–1194. doi: 10.1016/s0306-4522(97)00337-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Jenkins, T. M., Toosy, A. T., Ciccarelli, O., Miszkiel, K. A., Wheeler-Kingshott, C. A., Henderson, A. P., et al. (2010). Neuroplasticity predicts outcome of optic neuritis independent of tissue damage. Ann. Neurol. 67, 99–113. doi: 10.1002/ana.21823

PubMed Abstract | CrossRef Full Text | Google Scholar

Kalincik, T., Buzzard, K., Jokubaitis, V., Trojano, M., Duquette, P., Izquierdo, G., et al. (2014). Risk of relapse phenotype recurrence in multiple sclerosis. Mult. Scler. 20, 1511–1522. doi: 10.1177/1352458514528762

PubMed Abstract | CrossRef Full Text | Google Scholar

Kis, B., Rumberg, B., and Berlit, P. (2008). Clinical characteristics of patients with late-onset multiple sclerosis. J. Neurol. 255, 697–702. doi: 10.1007/s00415-008-0778-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Kneebone, I. I., Dunmore, E. C., and Evans, E. (2003). Symptoms of depression in older adults with multiple sclerosis (MS): comparison with a matched sample of younger adults. Aging Ment. Health 7, 182–185. doi: 10.1080/1360786031000101148

PubMed Abstract | CrossRef Full Text | Google Scholar

Lassmann, H., van Horssen, J., and Mahad, D. (2012). Progressive multiple sclerosis: pathology and pathogenesis. Nat. Rev. Neurol. 8, 647–656. doi: 10.1038/nrneurol.2012.168

PubMed Abstract | CrossRef Full Text | Google Scholar

Lefaucheur, J.-P. (2005). Transcranial magnetic stimulation: applications in neurology. Rev. Neurol. 161, 1121–1130. doi: 10.1016/S0035-3787(05)85182-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Lynch, M. A. (2015). Neuroinflammatory changes negatively impact on LTP: a focus on IL-1β. Brain Res. 1621, 197–204. doi: 10.1016/j.brainres.2014.08.040

PubMed Abstract | CrossRef Full Text | Google Scholar

Mahad, D. H., Trapp, P. B. D., and Lassmann, P. H. (2015). Pathological mechanisms in progressive multiple sclerosis. Lancet Neurol. 14, 183–193. doi: 10.1016/S1474-4422(14)70256-X

PubMed Abstract | CrossRef Full Text | Google Scholar

Mainero, C., Pantano, P., Caramia, F., and Pozzilli, C. (2006). Brain reorganization during attention and memory tasks in multiple sclerosis: insights from functional MRI studies. J. Neurol. Sci. 245, 93–98. doi: 10.1016/j.jns.2005.08.024

PubMed Abstract | CrossRef Full Text | Google Scholar

Malenka, R. C., and Bear, M. F. (2004). LTP and LTD: an embarrassment of riches. Neuron 44, 5–21. doi: 10.1016/j.neuron.2004.09.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Mancini, A., Gaetani, L., Di Gregorio, M., Tozzi, A., Ghiglieri, V., Calabresi, P., et al. (2017). Hippocampal neuroplasticity and inflammation: relevance for multiple sclerosis. Mult. Scler. Demyelinating Disord. 2:2. doi: 10.1186/s40893-017-0019-1

CrossRef Full Text | Google Scholar

Mandolesi, G., De Vito, F., Musella, A., Gentile, A., Bullitta, S., Fresegna, D., et al. (2017a). miR-142–3p is a key regulator of IL-1β-dependent synaptopathy in neuroinflammation. J. Neurosci. 37, 546–561. doi: 10.1523/JNEUROSCI.0851-16.2016

PubMed Abstract | CrossRef Full Text | Google Scholar

Mandolesi, G., Bullitta, S., Fresegna, D., Gentile, A., De Vito, F., Dolcetti, E., et al. (2017b). Interferon-γ causes mood abnormalities by altering cannabinoid CB1 receptor function in the mouse striatum. Neurobiol. Dis. 108, 45–53. doi: 10.1016/j.nbd.2017.07.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Mandolesi, G., Grasselli, G., Musella, A., Gentile, A., Musumeci, G., Sepman, H., et al. (2012). GABAergic signaling and connectivity on Purkinje cells are impaired in experimental autoimmune encephalomyelitis. Neurobiol. Dis. 46, 414–424. doi: 10.1016/j.nbd.2012.02.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Mandolesi, G., Musella, A., Gentile, A., Grasselli, G., Haji, N., Sepman, H., et al. (2013). Interleukin-1β alters glutamate transmission at purkinje cell synapses in a mouse model of multiple sclerosis. J. Neurosci. 33, 12105–12121. doi: 10.1523/JNEUROSCI.5369-12.2013

PubMed Abstract | CrossRef Full Text | Google Scholar

Mandolesi, G., Gentile, A., Musella, A., Fresegna, D., De Vito, F., Bullitta, S., et al. (2015). Synaptopathy connects inflammation and neurodegeneration in multiple sclerosis. Nat. Rev. Neurol. 11, 711–724. doi: 10.1038/nrneurol.2015.222

PubMed Abstract | CrossRef Full Text | Google Scholar

Matias-Guiu, J. A., Cortés-Martínez, A., Valles-Salgado, M., Oreja-Guevara, C., Pytel, V., Montero, P., et al. (2017). Functional components of cognitive impairment in multiple sclerosis: a cross-sectional investigation. Front. Neurol. 8:643. doi: 10.3389/fneur.2017.00643

PubMed Abstract | CrossRef Full Text | Google Scholar

Matt, S. M., and Johnson, R. W. (2016). Neuro-immune dysfunction during brain aging: new insights in microglial cell regulation. Curr. Opin. Pharmacol. 26, 96–101. doi: 10.1016/j.coph.2015.10.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Mattioli, F., Bellomi, F., Stampatori, C., Parrinello, G., and Capra, R. (2011). Depression, disability and cognitive impairment in multiple sclerosis: a cross sectional Italian study. Neurol. Sci. 32, 825–832. doi: 10.1007/s10072-011-0624-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Mori, F., Kusayanagi, H., Buttari, F., Centini, B., Monteleone, F., Nicoletti, C. G., et al. (2012). Early treatment with high-dose interferon β-1a reverses cognitive and cortical plasticity deficits in multiple sclerosis. Funct. Neurol. 27, 163–168.

PubMed Abstract | Google Scholar

Mori, F., Nisticò, R., Mandolesi, G., Piccinin, S., Mango, D., Kusayanagi, H., et al. (2014a). Interleukin-1β promotes long-term potentiation in patients with multiple sclerosis. Neuromolecular Med. 16, 38–51. doi: 10.1007/s12017-013-8249-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Mori, F., Kusayanagi, H., Nicoletti, C. G., Weiss, S., Marciani, M. G., and Centonze, D. (2014b). Cortical plasticity predicts recovery from relapse in multiple sclerosis. Mult. Scler. 20, 451–457. doi: 10.1177/1352458513512541

PubMed Abstract | CrossRef Full Text | Google Scholar

Mori, F., Rossi, S., Piccinin, S., Motta, C., Mango, D., Kusayanagi, H., et al. (2013). Synaptic plasticity and PDGF signaling defects underlie clinical progression in multiple sclerosis. J. Neurosci. 33, 19112–19119. doi: 10.1523/JNEUROSCI.2536-13.2013

PubMed Abstract | CrossRef Full Text | Google Scholar

Mori, F., Rossi, S., Sancesario, G., Codecà, C., Mataluni, G., Monteleone, F., et al. (2011). Cognitive and cortical plasticity deficits correlate with altered amyloid-β CSF levels in multiple sclerosis. Neuropsychopharmacology 36, 559–568. doi: 10.1038/npp.2010.187

PubMed Abstract | CrossRef Full Text | Google Scholar

Motl, R. W., and Pilutti, L. A. (2012). The benefits of exercise training in multiple sclerosis. Nat. Rev. Neurol. 8, 487–497. doi: 10.1038/nrneurol.2012.136

PubMed Abstract | CrossRef Full Text | Google Scholar

Motl, R. W., Sandroff, B. M., Kwakkel, G., Dalgas, U., Feinstein, A., Heesen, C., et al. (2017). Exercise in patients with multiple sclerosis. Lancet Neurol. 16, 848–856. doi: 10.1016/S1474-4422(17)30281-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Müller-Dahlhaus, J. F. M., Orekhov, Y., Liu, Y., and Ziemann, U. (2008). Interindividual variability and age-dependency of motor cortical plasticity induced by paired associative stimulation. Exp. Brain Res. 187, 467–475. doi: 10.1007/s00221-008-1319-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Nasios, G., Messinis, L., Dardiotis, E., and Papathanasopoulos, P. (2018). Review article repetitive transcranial magnetic stimulation, cognition, and multiple sclerosis: an overview. Behav. Neurol. 2018:8584653. doi: 10.1155/2018/8584653

PubMed Abstract | CrossRef Full Text | Google Scholar

Nicoll, R. A., and Malenka, R. C. (1999). Expression mechanisms underlying NMDA receptor-dependent long-term potentiation. Ann. N Y Acad. Sci. 868, 515–525. doi: 10.1111/j.1749-6632.1999.tb11320.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Nisticò, R., Mango, D., Mandolesi, G., Piccinin, S., Berretta, N., Pignatelli, M., et al. (2013). Inflammation subverts hippocampal synaptic plasticity in experimental multiple sclerosis. PLoS One 8:e54666. doi: 10.1371/journal.pone.0054666

PubMed Abstract | CrossRef Full Text | Google Scholar

Norden, D. M., and Godbout, J. P. (2013). Review: microglia of the aged brain: primed to be activated and resistant to regulation. Neuropathol. Appl. Neurobiol. 39, 19–34. doi: 10.1111/j.1365-2990.2012.01306.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Norden, D. M., Muccigrosso, M. M., and Godbout, J. P. (2015). Microglial priming andenhanced reactivity to secondary insult in aging and traumatic CNS injury, and neurodegenerative disease. Neuropharmacology 96, 29–41. doi: 10.1016/j.neuropharm.2014.10.028

PubMed Abstract | CrossRef Full Text | Google Scholar

Novotna, M., Paz Soldán, M. M., Abou Zeid, N., Kale, N., Tutuncu, M., Crusan, D. J., et al. (2015). Poor early relapse recovery affects onset of progressive disease course in multiple sclerosis. Neurology 85, 722–729. doi: 10.1212/WNL.0000000000001856

PubMed Abstract | CrossRef Full Text | Google Scholar

Ojo, J. O., Rezaie, P., Gabbott, P. L., and Stewart, M. G. (2015). Impact of age-related neuroglial cell responses on hippocampal deterioration. Front. Aging Neurosci. 7:57. doi: 10.3389/fnagi.2015.00057

PubMed Abstract | CrossRef Full Text | Google Scholar

Olsson, T., Barcellos, L. F., and Alfredsson, L. (2017). Interactions between genetic, lifestyle and environmental risk factors for multiple sclerosis. Nat. Rev. Neurol. 13, 25–36. doi: 10.1038/nrneurol.2016.187

PubMed Abstract | CrossRef Full Text | Google Scholar

Ontaneda, D., Thompson, A. J., Fox, R. J., and Cohen, J. A. (2017). Progressive multiple sclerosis: prospects for disease therapy, repair, and restoration of function. Lancet 389, 1357–1366. doi: 10.1016/S0140-6736(16)31320-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Pantano, P., Mainero, C., Domenico Iannetti, G., Caramia, F., Di Legge, S., Piattella, M. C., et al. (2002). Contribution of corticospinal tract damage to cortical motor reorganization after a single clinical attack of multiple sclerosis. Neuroimage 17, 1837–1843. doi: 10.1006/nimg.2002.1313

PubMed Abstract | CrossRef Full Text | Google Scholar

Pascual-Leone, A., Freitas, C., Oberman, L., Horvath, J. C., Halko, M., Eldaief, M., et al. (2011). Characterizing brain cortical plasticity and network dynamics across the age-span in health and disease with TMS-EEG and TMS-fMRI. Brain Topogr. 24, 302–315. doi: 10.1007/s10548-011-0196-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Patten, S. B., Beck, C. A., Williams, J. V., Barbui, C., and Metz, L. M. (2003). Major depression in multiple sclerosis: a population-based perspective. Neurology 61, 1524–1527. doi: 10.1212/01.wnl.0000095964.34294.b4

PubMed Abstract | CrossRef Full Text | Google Scholar

Patten, S. B., Metz, L. M., and Reimer, M. A. (2000). Biopsychosocial correlates of lifetime major depression in a multiple sclerosis population. Mult. Scler. 6, 115–120. doi: 10.1177/135245850000600210

PubMed Abstract | CrossRef Full Text | Google Scholar

Pelletier, J., Audoin, B., Reuter, F., and Ranjeva, J. P. (2009). Plasticity in MS: from functional imaging to rehabilitation. Int. MS J. 16, 26–31.

PubMed Abstract | Google Scholar

Penner, I. K., Rausch, M., Kappos, L., Opwis, K., and Radü, E. W. (2003). Analysis of impairment related functional architecture in MS patients during performance of different attention tasks. J. Neurol. 250, 461–472. doi: 10.1007/s00415-003-1025-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Phillips, L. J., and Stuifbergen, A. K. (2008). The influence of positive experiences on depression and quality of life in persons with multiple sclerosis. J. Holist. Nurs 26, 41–48. doi: 10.1177/0898010107301870

PubMed Abstract | CrossRef Full Text | Google Scholar

Pinter, D., Sumowski, J., DeLuca, J., Fazekas, F., Pichler, A., Khalil, M., et al. (2014). Higher education moderates the effect of T2 lesion load and third ventricle width on cognition in multiple sclerosis. PLoS One 9:e87567. doi: 10.1371/journal.pone.0087567

PubMed Abstract | CrossRef Full Text | Google Scholar

Pizza, V., Agresta, A., D’Acunto, C. W., Festa, M., and Capasso, A. (2011). Neuroinflamm-aging and neurodegenerative diseases: an overview. CNS Neurol. Disord. Drug Targets 10, 621–634. doi: 10.2174/187152711796235014

PubMed Abstract | CrossRef Full Text | Google Scholar

Planche, V., Gibelin, M., Cregut, D., Pereira, B., and Clavelou, P. (2016). Cognitive impairment in a population-based study of patients with multiple sclerosis: differences between late relapsing-remitting, secondary progressive and primary progressive multiple sclerosis. Eur. J. Neurol. 23, 282–289. doi: 10.1111/ene.12715

PubMed Abstract | CrossRef Full Text | Google Scholar

Polliack, M. L., Barak, Y., and Achiron, A. (2001). Late-onset multiple sclerosis. J. Am. Geriatr. Soc. 49, 168–171. doi: 10.1046/j.1532-5415.2001.49038.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Potagas, C., Giogkaraki, E., Koutsis, G., Mandellos, D., Tsirempolou, E., Sfagos, C., et al. (2008). Cognitive impairment in different MS subtypes and clinically isolated syndromes. J. Neurol. Sci. 267, 100–106. doi: 10.1016/j.jns.2007.10.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Ramachandran, S., Strange, R. C., Jones, P. W., Kalra, S., Nayak, D., and Hawkins, C. P. (2014). Associations between onset age and disability in multiple sclerosis patients studied using MSSS and a progression model. Mult. Scler. Relat. Disord. 3, 593–599. doi: 10.1016/j.msard.2014.06.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Rao, S. M. (1991). A Manual for the Brief, Repeatable Battery of Neuropsychological Tests in Multiple Sclerosis. New York, NY: National Multiple Sclerosis Society.

Reddy, H., Narayanan, S., Arnoutelis, R., Jenkinson, M., Antel, J., Matthews, P. M., et al. (2000a). Evidence for adaptive functional changes in the cerebral cortex with axonal injury from multiple sclerosis. Brain 123, 2314–2320. doi: 10.1093/brain/123.11.2314

PubMed Abstract | CrossRef Full Text | Google Scholar

Reddy, H., Narayanan, S., Matthews, P. M., Hoge, R. D., Pike, G. B., Duquette, P., et al. (2000b). Relating axonal injury to functional recovery in MS. Neurology 54, 236–239. doi: 10.1212/WNL.54.1.236

PubMed Abstract | CrossRef Full Text | Google Scholar

Reddy, H., Narayanan, S., Woolrich, M., Mitsumori, T., Lapierre, Y., Arnold, D. L., et al. (2002). Functional brain reorganization for hand movement in patients with multiple sclerosis: defining distinct effects of injury and disability. Brain 125, 2646–2657. doi: 10.1093/brain/awf283

PubMed Abstract | CrossRef Full Text | Google Scholar

Rocca, M. A., Amato, M. P., De Stefano, N., Enzinger, C., Geurts, J. J., Penner, I. K., et al. (2015). Clinical and imaging assessment of cognitive dysfunction in multiple sclerosis. Lancet Neurol. 14, 302–417. doi: 10.1016/S1474-4422(14)70250-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Rocca, M. A., Ceccarelli, A., Rodegher, M., Misci, P., Riccitelli, G., Falini, A., et al. (2010a). Preserved brain adaptive properties in patients with benign multiple sclerosis. Neurology 74, 142–149. doi: 10.1212/WNL.0b013e3181c91a00

PubMed Abstract | CrossRef Full Text | Google Scholar

Rocca, M. A., Valsasina, P., Absinta, M., Riccitelli, G., Rodegher, M. E., Misci, P., et al. (2010b). Default-mode network dysfunction and cognitive impairment in progressive MS. Neurology 74, 1252–1259. doi: 10.1212/WNL.0b013e3181d9ed91

PubMed Abstract | CrossRef Full Text | Google Scholar

Rocca, M. A., Colombo, B., Falini, A., Ghezzi, A., Martinelli, V., Scotti, G., et al. (2005). Cortical adaptation in patients with MS: a cross-sectional functional MRI study of disease phenotypes. Lancet Neurol. 4, 618–626. doi: 10.1016/s1474-4422(05)70171-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Rocca, M. A., Falini, A., Colombo, B., Scotti, G., Comi, G., and Filippi, M. (2002a). Adaptive functional changes in the cerebral cortex of patients with nondisabling multiple sclerosis correlate with the extent of brain structural damage. Ann. Neurol. 51, 330–339. doi: 10.1002/ana.10120

PubMed Abstract | CrossRef Full Text | Google Scholar

Rocca, M. A., Matthews, P. M., Caputo, D., Ghezzi, A., Falini, A., Scotti, G., et al. (2002b). Evidence for widespread movement-associated functional MRI changes in patients with PPMS. Neurology 58, 866–872. doi: 10.1212/WNL.58.6.866

PubMed Abstract | CrossRef Full Text | Google Scholar

Rocca, M. A., Gavazzi, C., Mezzapesa, D. M., Falini, A., Colombo, B., Mascalchi, M., et al. (2003a). A functional magnetic resonance imaging study of patients with secondary progressive multiple sclerosis. Neuroimage 19, 1770–1777. doi: 10.1016/s1053-8119(03)00242-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Rocca, M. A., Mezzapesa, D. M., Falini, A., Ghezzi, A., Martinelli, V., Scotti, G., et al. (2003b). Evidence for axonal pathology and adaptive cortical reorganization in patients at presentation with clinically isolated syndromes suggestive of multiple sclerosis. Neuroimage 18, 847–855. doi: 10.1016/s1053-8119(03)00043-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Rocca, M. A., Riccitelli, G. C., Meani, A., Pagani, E., Del Sette, P., Martinelli, V., et al. (2018). Cognitive reserve, cognition, and regional brain damage in MS: a 2 -year longitudinal study. Mult. Scler. doi: 10.1177/1352458517750767 [Epub ahead of print].

PubMed Abstract | CrossRef Full Text | Google Scholar

Rossi, S., Furlan, R., De Chiara, V., Motta, C., Studer, V., Mori, F., et al. (2012). Interleukin-1β causes synaptic hyperexcitability in multiple sclerosis. Ann. Neurol. 71, 76–83. doi: 10.1002/ana.22512

PubMed Abstract | CrossRef Full Text | Google Scholar

Rossi, S., Motta, C., Studer, V., Barbieri, F., Buttari, F., Bergami, A., et al. (2014). Tumor necrosis factor is elevated in progressive multiple sclerosis and causes excitotoxic neurodegeneration. Mult. Scler. 20, 304–312. doi: 10.1177/1352458513498128

PubMed Abstract | CrossRef Full Text | Google Scholar

Rossi, S., Muzio, L., De Chiara, V., Grasselli, G., Musella, A., Musumeci, G., et al. (2011). Impaired striatal GABA transmission in experimental autoimmune encephalomyelitis. Brain Behav. Immun. 25, 947–956. doi: 10.1016/j.bbi.2010.10.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Rossi, S., Studer, V., Motta, C., Polidoro, S., Perugini, J., Macchiarulo, G., et al. (2017). Neuroinflammation drives anxiety and depression in relapsing-remitting multiple sclerosis. Neurology 89, 1338–1347. doi: 10.1212/WNL.0000000000004411

PubMed Abstract | CrossRef Full Text | Google Scholar

Rossi, S., Studer, V., Moscatelli, A., Motta, C., Coghe, G., Fenu, G., et al. (2013). Opposite roles of NMDA receptors in relapsing and primary progressive multiple sclerosis. PLoS One 8:e67357. doi: 10.1371/journal.pone.0067357

PubMed Abstract | CrossRef Full Text | Google Scholar

Rossini, P. M., and Rossi, S. (2007). Transcranial magnetic stimulation: diagnostic, therapeutic, and research potential. Neurology 68, 484–488. doi: 10.1212/01.wnl.0000250268.13789.b2

PubMed Abstract | CrossRef Full Text | Google Scholar

Roy, S., Frndak, S., Drake, A. S., Irwin, L., Zivadinov, R., Weinstock-Guttman, B., et al. (2017). Differential effects of aging on motor and cognitive functioning in multiple sclerosis. Mult. Scler. 23, 1385–1393. doi: 10.1177/1352458516679036

PubMed Abstract | CrossRef Full Text | Google Scholar

Roy, S., Schwartz, C. E., Duberstein, P., Dwyer, M. G., Zivadinov, R., Bergsland, N., et al. (2016). Synergistic effects of reserve and adaptive personality in multiple sclerosis. J. Int. Neuropsychol. Soc. 22, 920–927. doi: 10.1017/S1355617716000333

PubMed Abstract | CrossRef Full Text | Google Scholar

Ruano, L., Portaccio, E., Goretti, B., Niccolai, C., Severo, M., Patti, F., et al. (2017). Age and disability drive cognitive impairment in multiple sclerosis across disease subtypes. Mult. Scler. 23, 1258–1267. doi: 10.1177/1352458516674367

PubMed Abstract | CrossRef Full Text | Google Scholar

Ruet, A., Deloire, M., Charré-Morin, J., Hamel, D., and Brochet, B. (2013). Cognitive impairment differs between primary progressive and relapsing-remitting MS. Neurology 80, 1501–1508. doi: 10.1212/WNL.0b013e31828cf82f

PubMed Abstract | CrossRef Full Text | Google Scholar

Sanai, S. A., Saini, V., Benedict, R. H., Zivadinov, R., Teter, B. E., Ramanathan, M., et al. (2016). Aging and multiple sclerosis. Mult. Scler. 22, 717–725. doi: 10.1177/1352458516634871

PubMed Abstract | CrossRef Full Text | Google Scholar

Sandroff, B. M., Balto, J. M., Klaren, R. E., Sommer, S. K., DeLuca, J., and Motl, R. W. (2016a). Systematically developed pilot randomized controlled trial of exercise and cognition in persons with multiple sclerosis. Neurocase 22, 443–450. doi: 10.1080/13554794.2016.1237658

PubMed Abstract | CrossRef Full Text | Google Scholar

Sandroff, B. M., Motl, R. W., Scudder, M. R., and DeLuca, J. (2016b). Systematic, evidence-based review of exercise, physical activity and physical fitness effects on cognition in persons with multiple sclerosis. Neuropsychol. Rev. 26, 271–294. doi: 10.1007/s11065-016-9324-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Sandroff, B. M., Klaren, R. E., Pilutti, L. A., Dlugonski, D., Benedict, R. H. B., and Motl, R. W. (2014). Randomized controlled trial of physical activity, cognition and walking in multiple sclerosis. J. Neurol. 261, 363–372. doi: 10.1007/s00415-013-7204-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Scalfari, A., Neuhaus, A., Daumer, M., DeLuca, G. C., Muraro, P. A., and Ebers, G. C. (2013). Early relapses, onset of progression and late outcome in multiple sclerosis. JAMA Neurol. 70, 214–222. doi: 10.1001/jamaneurol.2013.599

PubMed Abstract | CrossRef Full Text | Google Scholar

Scalfari, A., Neuhaus, A., Daumer, M., Ebers, G. C., and Muraro, P. A. (2011). Age and disability accumulation in multiple sclerosis. Neurology 77, 1246–1252. doi: 10.1212/WNL.0b013e318230a17d

PubMed Abstract | CrossRef Full Text | Google Scholar

Scalfari, A., Neuhaus, A., Degenhardt, A., Rice, G. P., Muraro, P. A., Daumer, M., et al. (2010). The natural history of multiple sclerosis, a geographically based study 10: relapses and long-term disability. Brain 133, 1914–1929. doi: 10.1093/brain/awq118

PubMed Abstract | CrossRef Full Text | Google Scholar

Schoonheim, M. M., Geurts, J. J. G., and Barkhof, F. (2010). The limits of functional reorganization in multiple sclerosis. Neurology 74, 1246–1247. doi: 10.1212/WNL.0b013e3181db9957

PubMed Abstract | CrossRef Full Text | Google Scholar

Schwartz, M., and Deczkowska, A. (2016). Neurological disease as a failure of brain-immune crosstalk: the multiple faces of neuroinflammation. Trends Immunol. 37, 668–679. doi: 10.1016/j.it.2016.08.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Stampanoni Bassi, M., Mori, F., Buttari, F., Marfia, G. A., Sancesario, A., Centonze, D., et al. (2017). Neurophysiology of synaptic functioning in multiple sclerosis. Clin. Neurophysiol. 128, 1148–1157. doi: 10.1016/j.clinph.2017.04.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Stangel, M. (2008). Neuroprotection and neuroregeneration in multiple sclerosis. J. Neurol. 255, 77–81. doi: 10.1007/s00415-008-6014-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Stankoff, B., Mrejen, S., Tourbah, A., Fontaine, B., Lyon-Caen, O., Lubetzki, C., et al. (2007). Age at onset determines the occurrence of the progressive phase of multiple sclerosis. Neurology 68, 779–781. doi: 10.1212/01.wnl.0000256732.36565.4a

PubMed Abstract | CrossRef Full Text | Google Scholar

Stellwagen, D., Beattie, E. C., Seo, J. Y., and Malenka, R. C. (2005). Differential regulation of AMPA receptor and GABA receptor trafficking by tumor necrosis factor-α. J. Neurosci. 25, 3219–3228. doi: 10.1523/JNEUROSCI.4486-04.2005

PubMed Abstract | CrossRef Full Text | Google Scholar

Stern, Y. (2002). What is cognitive reserve? Theory and research application of the reserve concept. J. Int. Neuropsychol. Soc. 8, 448–460. doi: 10.1017/s1355617702813248

PubMed Abstract | CrossRef Full Text | Google Scholar

Sumowski, J. F., Chiaravalloti, N., and DeLuca, J. (2009). Cognitive reserve protects against cognitive dysfunction in multiple sclerosis. J. Clin. Exp. Neuropsychol. 31, 913–926. doi: 10.1080/13803390902740643

PubMed Abstract | CrossRef Full Text | Google Scholar

Sumowski, J. F., Rocca, M. A., Leavitt, V. M., Riccitelli, G., Comi, G., DeLuca, J., et al. (2013). Brain reserve and cognitive reserve in multiple sclerosis: what you’ve got and how you use it. Neurology 80, 2186–2193. doi: 10.1212/WNL.0b013e318296e98b

PubMed Abstract | CrossRef Full Text | Google Scholar

Tedeholm, H., Skoog, B., Lisovskaja, V., Runmarker, B., Nerman, O., and Andersen, O. (2015). The outcome spectrum of multiple sclerosis: disability, mortality and a cluster of predictors from onset. J. Neurol. 262, 1148–1163. doi: 10.1007/s00415-015-7674-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Tomassini, V., Matthews, P. M., Thompson, A. J., Fuglø, D., Geurts, J. J., Johansen-Berg, H., et al. (2012). Neuroplasticity and functional recovery in multiple sclerosis. Nat. Rev. Neurol. 8, 635–646. doi: 10.1038/nrneurol.2012.179

PubMed Abstract | CrossRef Full Text | Google Scholar

Tremlett, H., Paty, D., and Devonshire, V. (2006). Disability progression in multiple sclerosis is slower than previously reported. Neurology 66, 172–177. doi: 10.1212/01.wnl.0000194259.90286.fe

PubMed Abstract | CrossRef Full Text | Google Scholar

Trojano, M., Liguori, M., Bosco Zimatore, G., Bugarini, R., Avolio, C., Paolicelli, D., et al. (2002). Age-related disability in multiple sclerosis. Ann. Neurol. 51, 475–480. doi: 10.1002/ana.10147

PubMed Abstract | CrossRef Full Text | Google Scholar

Tsivgoulis, G., Triantafyllou, H., Papageorgiou, C., Evangelopoulos, M. E., Kararizou, E., Sfagos, C., et al. (2007). Associations of the expanded disability status scale with anxiety and depression in multiple sclerosis outpatients. Acta Neurol. Scand. 115, 67–72. doi: 10.1111/j.1600-0404.2006.00736.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Viviani, B., and Boraso, M. S. (2011). Cytokines and neuronal channels: a molecular basis for age-related decline of neuronal function? Exp. Gerontol. 46, 199–206. doi: 10.1016/j.exger.2010.09.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Viviani, B., Bartesaghi, S., Gardoni, F., Vezzani, A., Behrens, M. M., Bartfai, T., et al. (2003). Interleukin-1β enhances NMDA receptor-mediated intracellular calcium increase through activation of the Src family of kinases. J. Neurosci. 23, 8692–8700. doi: 10.1523/jneurosci.23-25-08692.2003

PubMed Abstract | CrossRef Full Text | Google Scholar

Viviani, B., Gardoni, F., Bartesaghi, S., Corsini, E., Facchi, A., Galli, C. L., et al. (2006). Interleukin-1β released by gp120 drives neural death through tyrosine phosphorylation and trafficking of NMDA receptors. J. Biol. Chem. 281, 30212–30222. doi: 10.1074/jbc.m602156200

PubMed Abstract | CrossRef Full Text | Google Scholar

von Bernhardi, R., Eugenín-von Bernhardi, L., and Eugenín, J. (2015). Microglial cell dysregulation in brain aging and neurodegeneration. Front. Aging Neurosci. 7:124. doi: 10.3389/fnagi.2015.00124

PubMed Abstract | CrossRef Full Text | Google Scholar

von Bernhardi, R., Tichauer, J. E., and Eugenín, J. (2010). Aging-dependent changes of microglial cells and their relevance for neurodegenerative disorders. J. Neurochem. 112, 1099–1114. doi: 10.1111/j.1471-4159.2009.06537.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Walford, R. L. (1969). The immunological theory of aging. Immunol. Rev. 2, 171–171. doi: 10.1111/j.1600-065X.1969.tb00210.x

CrossRef Full Text | Google Scholar

Weiss, S., Mori, F., Rossi, S., and Centonze, D. (2014). Disability in multiple sclerosis: when synaptic long-term potentiation fails. Neurosci. Biobehav. Rev. 43, 88–99. doi: 10.1016/j.neubiorev.2014.03.023

PubMed Abstract | CrossRef Full Text | Google Scholar

Williams, R. M., Turner, A. P., Hatzakis, M., Bowen, J. D., Rodriquez, A. A., and Haselkorn, J. K. (2005). Prevalence and correlates of depression among veterans with multiple sclerosis. Neurology 64, 75–80. doi: 10.1212/01.WNL.0000148480.31424.2A

PubMed Abstract | CrossRef Full Text | Google Scholar

Zeller, D., and Classen, J. (2014). Plasticity of the motor system in multiple sclerosis. Neuroscience 283, 222–230. doi: 10.1016/j.neuroscience.2014.05.043

PubMed Abstract | CrossRef Full Text | Google Scholar

Zeller, D., aufm Kampe, K., Biller, A., Stefan, K., Gentner, R., Schütz, A., et al. (2010). Rapid-onset central motor plasticity in multiple sclerosis. Neurology 74, 728–735. doi: 10.1212/WNL.0b013e3181d31dcf

PubMed Abstract | CrossRef Full Text | Google Scholar

Zeydan, B., and Kantarci, O. H. (2018). Progressive Forms of multiple sclerosis: distinct entity or age-dependent phenomena. Neurol. Clin. 36, 163–171. doi: 10.1016/j.ncl.2017.08.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Ziemann, U., Paulus, W., Nitsche, M. A., Pascual-Leone, A., Byblow, W. D., Berardelli, A., et al. (2008). Consensus: motor cortex plasticity protocols. Brain Stimul. 1, 164–182. doi: 10.1016/j.brs.2008.06.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: aging, cognition, experimental autoimmune encephalomyelitis, multiple sclerosis, neurodegeneration, neuroinflammation, synaptic plasticity, synaptopathy

Citation: Musella A, Gentile A, Rizzo FR, De Vito F, Fresegna D, Bullitta S, Vanni V, Guadalupi L, Stampanoni Bassi M, Buttari F, Centonze D and Mandolesi G (2018) Interplay Between Age and Neuroinflammation in Multiple Sclerosis: Effects on Motor and Cognitive Functions. Front. Aging Neurosci. 10:238. doi: 10.3389/fnagi.2018.00238

Received: 30 March 2018; Accepted: 20 July 2018;
Published: 08 August 2018.

Edited by:

Brandi Ormerod, University of Florida, United States

Reviewed by:

Adelaide Fernandes, Faculdade de Farmácia, Universidade de Lisboa, Portugal
Daniel Ortuño-Sahagún, Universidad de Guadalajara, Mexico
Anna Maria Pittaluga, Università di Genova, Italy

Copyright © 2018 Musella, Gentile, Rizzo, De Vito, Fresegna, Bullitta, Vanni, Guadalupi, Stampanoni Bassi, Buttari, Centonze and Mandolesi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Diego Centonze, centonze@uniroma2.it

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