Sawangpong Jandee1,2
Annelies Geeraerts1Hannelore Geysen1Nathalie Rommel1,3
Jan Tack1,4
Tim Vanuytsel1,4*- 1Department of Chronic Diseases, Translational Research Center for Gastrointestinal Disorders (TARGID), Metabolism and Ageing (CHROMETA), KU Leuven, Leuven, Belgium
- 2Gastroenterology and Hepatology Unit, Department of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand
- 3Department of Neurosciences, Experimental Otorhinolaryngology, KU Leuven, Leuven, Belgium
- 4Department of Gastroenterology and Hepatology, Leuven University Hospitals, Leuven, Belgium
Esophageal hypomotility in general and especially ineffective esophageal motility according to the Chicago criteria of primary motility disorders of the esophagus, is one of the most frequently diagnosed motility disorders on high resolution manometry and results in a large number of patients visiting gastroenterologists. Most patients with esophageal hypomotility present with gastroesophageal reflux symptoms or dysphagia. The clinical relevance of the motility pattern, however, is not well established but seems to be correlated with disease severity in reflux patients. The correlation with dysphagia is less clear. Prokinetic agents are commonly prescribed as first line pharmacologic intervention to target esophageal smooth muscle contractility and improve esophageal motor functions. However, the beneficial effects of these medications are limited and only confined to some specific drugs. Serotonergic agents, including buspirone, mosapride and prucalopride have been shown to improve parameters of esophageal motility although the effect on symptoms is less clear. Understanding on the complex correlation between esophageal hypomotility and esophageal symptoms as well as the limited evidence of prokinetic agents is necessary for physicians to appropriately manage patients with Ineffective Esophageal Motility (IEM).
Introduction
High resolution manometry (HRM) is widely applied to evaluate esophageal motor function, resulting in a better recognition of esophageal motility disorders (Sweis et al., 2018). The most recently updated classification for esophageal motility disorders, the Chicago Classification version 3.0, was proposed in 2015 after two previous versions in 2008 and 2012. This classification was developed based on the analysis of clinical studies in healthy volunteers and patients, and categorized esophageal body motility disorders into major and minor disorders of peristalsis (Boland et al., 2016). Achalasia and major disorders of peristalsis, including distal esophageal spasm, jackhammer esophagus and absent contractility, reveal clinically relevant conditions for which evidence-based treatments are available—with the exception of absent contractility. This is in strong contrast with minor esophageal motility disorders, particularly ineffective esophageal motility (IEM), which still have unclear clinical implications and of which the management is not well established (Boland et al., 2016).
IEM is reported in as many as 30% of patients undergoing HRM. It is defined by the Chicago classification as over 50% of swallows being either weak or failed [Distal Contractile Integral (DCI) ≤450 mmHg s cm], while normal lower esophageal sphincter relaxation is preserved [normal Integrated Relaxation Pressure (IRP)] (Figure 1) (Kahrilas et al., 2015).
FIGURE 1. Esophageal high-resolution manometry demonstrating Ineffective Esophageal Motility (IEM) (A) failed peristalsis (DCI <100 mmHg s cm) and (B) weak peristalsis (DCI 100–450 mmHg s cm). IEM, ineffective esophageal motility; DCI, distal contractile integral.
In this narrative review, we summarize the available literature on the clinical associations of a manometric diagnosis of IEM and its treatment with prokinetics. A PubMed literature search was performed that included published articles in English through October 31, 2020 with combinations of the terms “ineffective esophageal motility,” “high resolution manometry,” “clinical relevance,” “pharmacological treatment,” and “prokinetic.” Reference lists of the retrieved articles were also searched for additional articles.
Esophageal Hypomotility and Esophageal Symptoms
IEM is one of the most frequent findings on esophageal HRM. However, the association of esophageal hypomotility with symptoms is still controversial which makes this a confusing diagnostic entity. A prospective study of Hollenstein et al. in healthy volunteers revealed that as many as 17% of asymptomatic subjects demonstrated a pattern of IEM on routine esophageal manometry (Hollenstein et al., 2017). Moreover, IEM is detected in patients with a variety of esophageal symptoms, particularly gastroesophageal reflux symptoms and dysphagia, but these symptoms are not discriminative of IEM. A retrospective study from China evaluated 256 dysphagia patients who had unremarkable findings on esophagogastroscopy and underwent HRM. In this population IEM was the most common feature, in 38.6% of patients (Wang et al., 2019). However, several studies failed to demonstrate a correlation between IEM and esophageal symptoms (Xiao et al., 2014; Shetler et al., 2017). Indeed, proportions of heartburn, regurgitation, dysphagia, chest pain, and belching were similar in patients with and without IEM in observational studies (Min et al., 2015; Shetler et al., 2017). In addition, the correlation of the perception of dysphagia with abnormal bolus transit resulting from weak or absent peristalsis is also limited (Lazarescu et al., 2010; Roman et al., 2011).
IEM is more prevalent in smooth muscle disorders, such as scleroderma and other connective tissue disorders (Carlson et al., 2016). Moreover, phosphodiesterase inhibitors, calcium channel blockers and non-benzodiazepine antispasmodic agents can reduce esophageal contraction vigor and should be avoided in patients with esophageal hypomotility (Simren et al., 2003; Rangan et al., 2018).
Esophageal Motor Dysfunction and Gastroesophageal Reflux Disease
Available data indicate that Gastroesophageal Reflux Disease (GERD) results from multiple predisposing factors in upper gastrointestinal motility, especially transient lower esophageal sphincter relaxations (TLESRs) (Schneider et al., 2010) which are more likely to be associated with reflux in GERD patients (Sifrim et al., 2001). In addition, esophageal body hypomotility is also more frequent in pH-monitoring proven GERD (Chan et al., 2011; Savarino et al., 2017).
Impaired esophageal clearance of the refluxate caused by ineffective primary and secondary peristalsis has also been illustrated in a higher proportion of patients with erosive esophagitis compared to a non-erosive reflux disease group (29 vs. 15%; p = 0.030) (Wu et al., 2007; Chen et al., 2014). Furthermore, the study of Wang et al. also demonstrated that erosive esophagitis and increasing GERD symptom severity are consistently associated with a greater likelihood of IEM, while the prevalence of IEM in non-erosive reflux disease and physiologic acid exposure is low (Wang et al., 2009). Additionally, severe IEM, defined as over 70% ineffective peristalsis, provides supportive evidence for a more severe GERD phenotype with an increased acid exposure in supine position (Shetler et al., 2017; Rengarajan et al., 2018). These data suggest a role for IEM in the pathophysiology of GERD. However, a case could also be made that esophageal hypomotility may result from increased reflux exposure. Longitudinal data, studying the sequence between GERD and esophageal hypomotility, are not available, but improvement of hypocontractility after anti-reflux surgery has been reported, suggesting that successful anti-reflux treatment may correct esophageal dysmotility (Munitiz et al., 2004). However, prolonged proton pump inhibitor (PPI) treatment in 23 patients with severe erosive esophagitis did not correct esophageal hypomotility (Xu et al., 2007). In a recent study on the reproducibility of esophageal manometric diagnoses, PPI treatment was not clearly associated with improved motility in esophageal hypomotility (Sandhu et al., 2020).
Natural History and Prognosis
There is limited understanding of the natural history of IEM. However, IEM does not progress over time, and quality of life does not seem to be much impacted (Ravi et al., 2015). Patients with this minor esophageal motor abnormality reported minimal symptoms and needed few medical interventions during long-term follow-up over 6 years. Interestingly, the presence of peristaltic reserve by provocative maneuvers including multiple rapid swallowing (MRS) predicted a better prognosis and efficacy of prokinetics (Min et al., 2015; Gyawali et al., 2019).
General Pharmacological Management
Pharmacologic interventions that are able to improve esophageal smooth muscle contractility or associated symptoms, are still limited and poorly effective (Smout and Fox, 2012). There is also no clear directive on when IEM needs management, as symptoms (e.g., dysphagia) and even GERD is not consistently identified with IEM. Therefore—unless GERD is identified—the decision if and how symptomatic patients with IEM should be treated, is challenging.
Diet, lifestyle modification and medical GERD management remain the cornerstone of therapy (Triadafilopoulos et al., 2016). Basically, acid-suppressive medication will treat reflux and reflux-related symptoms but it may not improve esophageal motor function (Xu et al., 2007; Sandhu et al., 2020). Besides PPI therapy, prokinetic agents are advised in GERD patients with esophageal motility disorders and PPI-refractory symptoms to enhance clearance of the refluxed contents (Scarpellini et al., 2016; Lin et al., 2019).
Taking into account the limitations of IEM in terms of correlation to symptoms and GERD, we propose an algorithm to guide clinical decision making on prokinetic prescription in patients with esophageal hypomotility (Figure 2).
FIGURE 2. Algorithm for decision making on prokinetic prescription in patients with esophageal hypomotility. IEM, ineffective esophageal motility; GERD, gastroesophageal reflux disease.
Prokinetic Treatment
Esophageal peristalsis results from a concerted contraction and relaxation of circular and longitudinal musculature to propel the ingested food bolus toward the stomach. Peristalsis in the proximal esophagus, which is composed entirely of striated muscle, is dependent on central mechanisms, involving sequential activation of vagal lower motor neurons originating from the nucleus ambiguous (Kahrilas and Boeckxstaens, 2013). In contrast, distal esophageal peristalsis, which is mainly composed of smooth muscle fibers, is controlled by both central input, but mainly orchestrated by the ganglia of the enteric nervous system in the esophageal wall (Figure 3). There are two types of postganglionic myenteric motor neurons: excitatory neurons releasing the neurotransmitter acetylcholine (ACh), and inhibitory neurons that contain nitric oxide (NO) and vasoactive intestinal polypeptide (VIP). The balanced activation and interaction between these neurons and neurotransmitters are critical for the normal peristaltic function of the esophagus (Park and Conklin, 1999) and can be targeted by pharmacologic interventions, using prokinetics, in patients with severe esophageal hypomotility or absent contractility to restore esophageal motor function (Table 1; Figure 4). In patients with mild esophageal hypomotility we recommend a conservative approach taking into account the limited available clinical evidence and benign natural history. We also propose a hierarchy in the use of the available prokinetics based on the efficacy data and adverse events (Figure 4). In this overview we did not focus on cisapride and tegaserod because these drugs have been withdrawn from the market because of cardiovascular adverse events. Although tegaserod has been re-approved in 2019, the specific indication was limited to female patients with constipation predominant irritable bowel syndrome.
FIGURE 3. Schematic overview demonstrating the motor innervation of the esophagus and pharmacological targets to enhance esophageal peristalsis. Dashed line signify uncertainty of the exact receptor localization. DMN, Dorsal motor nucleus; Ach, Acetylcholine; NO, Nitric oxide; VIP, Vasoactive intestinal polypeptide; 5-HT, 5-Hydroxytryptamine; M, Muscarinic; DA, Dopamine.
TABLE 1. Potentially beneficial prokinetic medications for esophageal hypomotility that have been studied in patients.
FIGURE 4. Guided algorithm illustrating prokinetic drugs application in setting of esophageal hypomotility GERD, Gastroesophageal reflux disease; IEM, Ineffective esophageal motility; 5-HT, 5-Hydroxytrptamine.
Dopamine 2 Receptor Blockers
Metoclopramide augmented esophageal contraction in healthy volunteers (Mikami et al., 2016) but in IEM, this conventional prokinetic agent is not beneficial (Gyawali et al., 2019). The acute effects of oral metoclopramide (40 mg/day) and domperidone (80 mg/day) on esophageal motor activity and acid reflux has been assessed in a randomized, double-blind, placebo-controlled study in 20 patients with erosive esophagitis. Both drugs caused a significant increase in lower esophageal sphincter (LES) pressure. However, neither esophageal body motility nor duration of esophageal acid exposure were affected by the prokinetics in comparison to placebo (Grande et al., 1992). Both domperidone (QT prolongation) and metoclopramide (extrapyramidal manifestations) have been associated with relevant adverse events, which are potentially serious (Leelakanok et al., 2016; Svendsen et al., 2018). In view of the lack of substantial efficacy they should probably not be used when attempting to treat esophageal hypomotility.
Serotonin Modulating Agents
Buspirone
Buspirone, an anxiolytic drug, is a partial agonist for 5-HT (hydroxytryptamine) 1A receptors, as well as an antagonist for dopamine D2 autoreceptors, with some evidence of a weak agonistic effect on 5-HT2 receptors (Loane and Politis, 2012). In the enteric nervous system, 5-HT1A receptors activation can release ACh from the nerve terminals and then stimulate esophageal motor function by muscarinic receptors on smooth muscle cells. (Eduard et al., 2017). Buspirone has been shown to augment esophageal peristaltic amplitude in healthy volunteers. Blonski et al. and Di Stefano et al. administered 20 mg of buspirone to healthy adults and measured esophageal motility by conventional manometry within 60 min of administration in a blinded, placebo-controlled trial. The mean distal esophageal amplitude and duration were increased in both studies after a single dose of buspirone (Blonski et al., 2009; Di Stefano et al., 2012).
In systemic sclerosis (SSc), Karamanolis et al. evaluated 21 consecutive symptomatic patients with esophageal hypomotility, using a one-time dose of 10 mg buspirone compared to 10 mg domperidone. They found an increased resting lower esophageal sphincter (LES) pressure after buspirone, but no other significant change in esophageal peristalsis (Karamanolis et al., 2015). Another study of the same group, showed the same results in a non-randomized open-label trial of 4 weeks of 20 mg buspirone dosage in 22 SSc patients (Karamanolis et al., 2016). However, patients with SSc are a specific group within the spectrum of esophageal hypomotility and in many patients, esophageal manometry will show absent contractility rather than IEM. Even if the data are limited, the pathophysiological mechanisms underlying esophageal dysmotility in SSc are probably due to a complex interplay of vascular, immune, and neural abnormalities. Pharmacological therapy may provide some benefit in neuropathic and myopathic dysfunction, while it will most likely not be efficient in later stages of fibrosis (Suto and Czirjak, 2009; Scheerens et al., 2015).
Recently, buspirone was studied in IEM and functional dysphagia patients, but there was no statistically significant difference in the high resolution esophageal parameters measured, as well as symptom outcomes compared to placebo (Table 1) (Aggarwal et al., 2018).
Mosapride
Mosapride is a 5-HT4 receptor agonist, and its metabolites also have a weak 5-HT3 antagonistic effect. Mosapride has no affinity for 5-HT1, 5-HT2 or dopamine D2 receptors. In 20 asymptomatic volunteers, mosapride 3 mg t.i.d. for 3 days increased the rate of complete bolus transit and accelerated esophageal bolus transit in a randomized double-blind crossover design (Cho et al., 2006). It has also been demonstrated that a single 40 mg dose of mosapride increased the likelihood of secondary peristaltic responses to abrupt intra-esophageal air distension (Chen et al., 2011). Another study in nine healthy volunteers by Fukazawa et al. (2014) revealed that mosapride 40 mg augmented peristaltic contractions, especially in the distal esophageal segments (Fukazawa et al., 2014).
In GERD patients, mosapride was significantly more effective than placebo in decreasing the total number of reflux episodes (Ruth et al., 1998). Moreover, a high dose of mosapride (90 mg/day) has been reported to improve esophageal motor function and acid reflux parameters (Ruth et al., 2003).
In IEM patients, a single high-dose of mosapride (40 mg) decreased the threshold volume of secondary peristalsis during rapid air distension compared with placebo, but had limited effect on the motor properties (Chen et al., 2013). A partial effect of mosapride on esophageal motility has only been shown with high dose, in contrast to low or standard dose (15 mg/day) which did not change the esophageal motility parameters (Koshino et al., 2010).
Prucalopride
Prucalopride is an enterokinetic agent which acts by facilitating the release of ACh from neurons of the myenteric plexus via a high affinity and specificity for 5-HT4 receptors (Briejer et al., 2001). Because of its highly specific effect on the 5-HT4 receptor in the absence of affinity for the hERG cardiac potassium channel, no cardiac toxicity has been reported in contrast to older 5-HT4 agonists, including cisapride (De Maeyer et at., 2008; Tack et al., 2012). Acute administration of 4 mg prucalopride enhanced mechanosensitivity of distension-induced secondary peristalsis and promoted esophageal contractility in 11 healthy adults (Yi et al., 2016). Kessing et al. demonstrated that 4 mg-prucalopride for 6 days in 21 healthy subjects reduced esophageal acid exposure and accelerated gastric emptying without significant effects on esophageal motility (Kessing et al., 2014).
In GERD patients with IEM, a single-dose of prucalopride enhanced primary and secondary peristalsis. The threshold volume for triggering secondary peristalsis during slow and rapid injection of air into esophagus was decreased, with limited impact on secondary peristaltic amplitude (Lei et al., 2018).
Sumatriptan
Sumatriptan is a 5-HT1D receptor agonist used in the treatment of migraine. In 3–5% of the patients this medication triggered chest symptoms which were hypothesized to originate from esophageal hypercontractility (Brown et al., 1991). In 16 healthy volunteers, one subcutaneous injection of 6 mg of sumatriptan significantly altered esophageal motor function with higher amplitude of esophageal contractions (Foster et al., 1999).
In patients with dysphagia and chest pain with IEM on manometry, a subcutaneous injection of sumatriptan increased the number of swallows and primary peristaltic waves, but not the amplitude or propagation velocity of esophageal motility (Grossi et al., 2003).
Motilin Receptor Agonists
Erythromycin
Erythromycin is an old macrolide antibiotic with prokinetic properties. The prokinetic action of erythromycin has been mainly attributed to its property of activating motilin receptors on smooth muscle fibers (Sanger et al., 2013). Its prokinetic efficacy was studied in GERD patients with a significant increase of the amplitude, duration, velocity and strength of esophageal peristalsis after a single intravenously administered dose (Chrysos et al., 2001).
Furthermore, oral erythromycin improved esophageal and gastric motility in diabetic patients and also resulted in a better control of blood sugar. The esophageal transit time, evaluated by radionuclide labeled liquid and solid meals, was significantly shorter (Chang et al., 2003). Another study from Taiwan reported an improvement of esophageal hypomotility in 15 diabetic patients, as evaluated by a non-invasive radionuclide esophageal transit test (Tsai et al., 1995). Despite a possible benefit on esophageal motility, disadvantages, including the risk of inducing microbial resistance, tachyphylaxis and cardiac dysrhythmia (QTc prolongation), should be taken into consideration (Goossens et al., 2005; Ray, et al., 2004).
Muscarinic Receptor Modulating Agents
Bethanechol
Bethanechol, a direct-acting muscarinic receptor agonist, has been used in the past as a promotility agent for treating GERD. This drug acts by mimicking the effect of ACh directly at the postganglionic cholinergic receptors, and has been shown to increase the LES pressure and improve esophageal peristaltic pressures in healthy volunteers (Ramirez and Richter, 1993).
In patients with severe IEM, oral bethanechol has been shown to significantly improve contraction pressures, distal esophageal amplitude and complete bolus transit of the esophagus (Agrawal et al., 2007). A retrospective chart review of 26 patients with a known diagnosis of IEM who were treated with bethanechol at the esophageal disorders clinic, also reported a positive response, defined as improvement of dysphagia, in 50% of patients (Grevenitis et al., 2012). However, more than a quarter of patients discontinued the treatment due to intolerable cholinergic side effects, including nausea, somnolence and increased urinary frequency.
Conclusion and Future Direction
It is important to emphasize that esophageal hypomotility is a manometric diagnosis that can be seen in healthy asymptomatic individuals and does not necessarily have a clear relevance in esophageal symptoms. Prokinetic agents can be considered in patients with esophageal symptoms thought to originate from IEM. However, currently available conventional prokinetic agents (mainly dopamine-2 antagonists) have not shown ability to restore the esophageal motor function in IEM. The potentially beneficial pharmacological agents are confined to specific serotonergic agents and motilin receptor agonists, but the scientific evidence is limited and larger future studies with a double-blind, randomized controlled design potentially including simultaneously impedance monitoring for bolus flow are needed to clearly identify its efficacy and clinical implication in patients with esophageal hypomotility.
Author Contributions
SJ performed the literature review. SJ and TV drafted the first manuscript. AG, HG, NR, and JT revised the manuscript and provided substantial comments.
Funding
JT is supported by a Methusalem grant of KU Leuven and TV is a senior clinical investigator of the Flanders Research Foundation (FWO Vlaanderen).
Conflict of Interest
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.
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Keywords: esophageal hypomotility, ineffective esophageal motility, high resolution manometry, prokinetic, gastroesophageal reflux, dysphagia
Citation: Jandee S, Geeraerts A, Geysen H, Rommel N, Tack J and Vanuytsel T (2021) Management of Ineffective Esophageal Hypomotility. Front. Pharmacol. 12:638915. doi: 10.3389/fphar.2021.638915
Received: 07 December 2020; Accepted: 12 May 2021;
Published: 26 May 2021.
Edited by:
Stefano Fiorucci, University of Perugia, ItalyReviewed by:
Dan-Lucian Dumitraşcu, Iuliu Haieganu University of Medicine and Pharmacy, RomaniaRinaldo Pellicano, Molinette Hospital, Italy
Copyright © 2021 Jandee, Geeraerts, Geysen, Rommel, Tack and Vanuytsel. 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: Tim Vanuytsel, dGltLnZhbnV5dHNlbEBrdWxldXZlbi5iZQ==