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Multiple Sclerosis Is Associated With Achalasia and Diffuse Esophageal Spasm

BACKGROUND/AIMS: Multiple sclerosis (MS) is an inflammatory disease characterized by the demyelination of primarily the central nervous system. Diffuse esophageal spasm (DES) and achalasia are disorders of esophageal peristalsis and esophagogastric junction outflow, respectively, which cause clinica...

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Autores principales: Kim, Yeseong, Shibli, Fahmi, Fu, Yuhan, Song, Gengqing, Fass, Ronnie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Neurogastroenterology and Motility 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577467/
https://www.ncbi.nlm.nih.gov/pubmed/37528077
http://dx.doi.org/10.5056/jnm22173
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author Kim, Yeseong
Shibli, Fahmi
Fu, Yuhan
Song, Gengqing
Fass, Ronnie
author_facet Kim, Yeseong
Shibli, Fahmi
Fu, Yuhan
Song, Gengqing
Fass, Ronnie
author_sort Kim, Yeseong
collection PubMed
description BACKGROUND/AIMS: Multiple sclerosis (MS) is an inflammatory disease characterized by the demyelination of primarily the central nervous system. Diffuse esophageal spasm (DES) and achalasia are disorders of esophageal peristalsis and esophagogastric junction outflow, respectively, which cause clinical symptoms of dysphagia. Mechanisms involving dysfunction of the pre- and post-ganglionic nerve fibers of the myenteric plexus have been proposed. We sought to determine whether MS confers an increased risk of developing achalasia or DES. METHODS: Cohort analysis was done using the Explorys database. Univariate logistic regression was performed to determine the odds MS confers to each motility disorder studied. Comparison of proportions of dysautonomia comorbidities was performed among the cohorts. Patients with a prior diagnosis of diabetes mellitus, chronic Chagas’ disease, opioid use, or CREST syndrome were excluded from the study. RESULTS: Odds of MS patients developing achalasia or DES were (OR, 2.09; 95% CI, 1.73-2.52; P < 0.001) and (OR, 3.15; 95% CI, 2.89-3.42; P < 0.001), respectively. In the MS/achalasia cohort, 27.27%, 18.18%, 9.09%, and 45.45% patients had urinary incontinence, gastroparesis, impotence, and insomnia, respectively. In the MS/DES cohort, 35.19%, 11.11%, 3.70%, and 55.56% had these symptoms. In MS patients without motility disorders, 12.64%, 0.79%, 2.21%, and 21.85% had these symptoms. CONCLUSIONS: Patients with MS have higher odds of developing achalasia or DES compared to patients without MS. MS patients with achalasia or DES have higher rates of dysautonomia comorbidities. This suggests that these patients have a more severe disease phenotype in regards to the extent of neuronal degradation and demyelination causing the autonomic dysfunction.
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spelling pubmed-105774672023-10-30 Multiple Sclerosis Is Associated With Achalasia and Diffuse Esophageal Spasm Kim, Yeseong Shibli, Fahmi Fu, Yuhan Song, Gengqing Fass, Ronnie J Neurogastroenterol Motil Original Article BACKGROUND/AIMS: Multiple sclerosis (MS) is an inflammatory disease characterized by the demyelination of primarily the central nervous system. Diffuse esophageal spasm (DES) and achalasia are disorders of esophageal peristalsis and esophagogastric junction outflow, respectively, which cause clinical symptoms of dysphagia. Mechanisms involving dysfunction of the pre- and post-ganglionic nerve fibers of the myenteric plexus have been proposed. We sought to determine whether MS confers an increased risk of developing achalasia or DES. METHODS: Cohort analysis was done using the Explorys database. Univariate logistic regression was performed to determine the odds MS confers to each motility disorder studied. Comparison of proportions of dysautonomia comorbidities was performed among the cohorts. Patients with a prior diagnosis of diabetes mellitus, chronic Chagas’ disease, opioid use, or CREST syndrome were excluded from the study. RESULTS: Odds of MS patients developing achalasia or DES were (OR, 2.09; 95% CI, 1.73-2.52; P < 0.001) and (OR, 3.15; 95% CI, 2.89-3.42; P < 0.001), respectively. In the MS/achalasia cohort, 27.27%, 18.18%, 9.09%, and 45.45% patients had urinary incontinence, gastroparesis, impotence, and insomnia, respectively. In the MS/DES cohort, 35.19%, 11.11%, 3.70%, and 55.56% had these symptoms. In MS patients without motility disorders, 12.64%, 0.79%, 2.21%, and 21.85% had these symptoms. CONCLUSIONS: Patients with MS have higher odds of developing achalasia or DES compared to patients without MS. MS patients with achalasia or DES have higher rates of dysautonomia comorbidities. This suggests that these patients have a more severe disease phenotype in regards to the extent of neuronal degradation and demyelination causing the autonomic dysfunction. The Korean Society of Neurogastroenterology and Motility 2023-10-30 2023-10-30 /pmc/articles/PMC10577467/ /pubmed/37528077 http://dx.doi.org/10.5056/jnm22173 Text en © 2023 The Korean Society of Neurogastroenterology and Motility https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Yeseong
Shibli, Fahmi
Fu, Yuhan
Song, Gengqing
Fass, Ronnie
Multiple Sclerosis Is Associated With Achalasia and Diffuse Esophageal Spasm
title Multiple Sclerosis Is Associated With Achalasia and Diffuse Esophageal Spasm
title_full Multiple Sclerosis Is Associated With Achalasia and Diffuse Esophageal Spasm
title_fullStr Multiple Sclerosis Is Associated With Achalasia and Diffuse Esophageal Spasm
title_full_unstemmed Multiple Sclerosis Is Associated With Achalasia and Diffuse Esophageal Spasm
title_short Multiple Sclerosis Is Associated With Achalasia and Diffuse Esophageal Spasm
title_sort multiple sclerosis is associated with achalasia and diffuse esophageal spasm
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577467/
https://www.ncbi.nlm.nih.gov/pubmed/37528077
http://dx.doi.org/10.5056/jnm22173
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