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SYSTEMATIC REVIEW article
Front. Dement.
Sec. Dementia Care
Volume 4 - 2025 |
doi: 10.3389/frdem.2025.1513644
This article is part of the Research Topic Characterizing and Measuring
Behavioral and Psychological Symptoms of Dementia (BPSD) View all 8 articles
Investigating Neuropathological Correlates of Hyperactive and Psychotic Symptoms in Dementia: A Systematic Review
Provisionally accepted- 1 Milan Center for Neuroscience, Department of Medicine and Surgery, University of Milano Bicocca, Milan, Lombardy, Italy
- 2 Department of Neurology and Neuropathology, Golgi-Cenci Foundation, Abbiategrasso, Italy
- 3 Unit of Biostatistics, Golgi-Cenci Foundation, Abbiategrasso, Milan, Italy
- 4 Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Lombardy, Italy
- 5 Department of Neurology, San Gerardo Hospital, Monza, Italy
- 6 Unit of Behavioral Neurology, Neurological Institute Foundation Casimiro Mondino (IRCCS), Pavia, Lombardy, Italy
- 7 Department of Rehabilitation ASP Golgi-Redaelli, Abbiategrasso, Milan, Italy
Behavioral and Psychological Symptoms of Dementia (BPSD) are common neuropsychiatric manifestations that complicate the clinical course of dementia and impact caregiving. Among these, the Hyperactivity-Impulsivity-Irritiability-Disinhibition-Aggression-Agitation (HIDA) and Psychosis (P) domains are particularly challenging to manage. Despite their prevalence, their underlying mechanisms and neuropathological correlates, remain poorly understood. This systematic review aims to elucidate the neuropathological basis of the HIDA and psychosis domains, exploring whether distinct proteinopathies and neural circuit dysfunctions are associated with these symptoms. The review follows PRISMA guidelines, with a systematic search conducted across MEDLINE, CENTRAL, and EMBASE databases. Inclusion criteria involved studies exploring the neuropathology of the HIDA and psychosis domains in individuals with dementia. Records were screened using PICO software, and data quality was assessed using the Newcastle-Ottawa Scale (NOS) and CARE guidelines. A narrative synthesis was conducted due to heterogeneity in the data. From 846 records identified, 37 studies met inclusion criteria. Of the 18823 cases analyzed, the most common diagnoses were Alzheimer's Disease (83.44%), Dementia with Lewy Bodies (5.37%), and Frontotemporal Dementia (13.40%). HIDA-P symptoms were distributed across all clinical diagnoses, with agitation (14.00%), delusions (11.60%), disinhibition (7.61%), and hallucinations (6.83%) being the most frequently reported behaviors. The primary neuropathological diagnosis was Alzheimer's Disease Neuropathologic Change (ADNC), present predominantly in intermediate to severe forms. The neuropathological analysis revealed the co-occurrence of multiple proteinopathies, particularly TAUopathy, TDP-43 pathology, and Lewy-related pathology (LRP), with the latter, in association with ADNC, reported in 15 studies. HIDA-P symptoms were linked with overlapping involvement of different neural circuits, particularly the amygdala and the broader limbic system. Evidence suggests that TAUopathy and multiple proteinopathies in key brain regions, such as amygdala, are central to the development of these symptoms. In contrast, the contribution of betaamyloid and vascular damage appears marginal in the genesis of HIDA and psychotic symptoms. No behavioral symptom is pathognomonic of a specific proteinopathy; rather, the topography and severity of lesions plays a more decisive role than their single molecular composition.
Keywords: Neuropathology, BPSD, Neuropsychiatric symptoms, psychosis, Dementia, Alzheimer, Lewy Bodies, FTLD
Received: 18 Oct 2024; Accepted: 09 Jan 2025.
Copyright: © 2025 Negro, Rossi, Imbimbo, Gatti, Magi, Appollonio, Costa and Poloni. 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) or licensor 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:
Tino Emanuele Poloni, Department of Neurology and Neuropathology, Golgi-Cenci Foundation, Abbiategrasso, Italy
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