Multiple Sclerosis Is Associated With Achalasia and Diffuse Esophageal Spasm.

IF 3.3 3区 医学 Q2 CLINICAL NEUROLOGY
Journal of Neurogastroenterology and Motility Pub Date : 2023-10-30 Epub Date: 2023-08-02 DOI:10.5056/jnm22173
Yeseong Kim, Fahmi Shibli, Yuhan Fu, Gengqing Song, Ronnie Fass
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引用次数: 0

Abstract

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 both disorders of esophageal peristalsis 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.

多发性硬化与贲门失弛缓症和弥漫性食管痉挛有关。
背景/目的:多发性硬化症(MS)是一种以中枢神经系统脱髓鞘为主要特征的炎症性疾病。弥漫性食管痉挛(DES)和贲门失弛缓症都是引起临床吞咽困难症状的食管蠕动障碍。肌间丛节前和节后神经纤维功能障碍的机制已经提出。我们试图确定MS是否会增加患贲门失弛缓症或DES的风险。方法:使用Explorys数据库进行队列分析。进行单变量逻辑回归,以确定MS赋予所研究的每种运动障碍的几率。比较各队列中自主神经功能障碍合并症的比例。既往诊断为糖尿病、慢性恰加斯病、阿片类药物使用或CREST综合征的患者被排除在研究之外。结果:MS患者发生贲门失弛缓症或DES的几率分别为(or,2.09;95%可信区间,1.73-2.52;P<0.001)和(or,3.15;95%置信区间,2.89-3.42;P>0.001)。在MS/贲门失弛缓症队列中,27.27%、18.18%、9.09%和45.45%的患者分别患有尿失禁、胃轻瘫、阳痿和失眠。在MS/DES队列中,35.19%、11.11%、3.70%和55.56%有这些症状。在没有运动障碍的MS患者中,12.64%、0.79%、2.21%和21.85%有这些症状。结论:与没有MS的患者相比,患有MS的患者发展为贲门失弛缓症或DES的几率更高。这表明,这些患者在引起自主神经功能障碍的神经元退化和脱髓鞘程度方面具有更严重的疾病表型。
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来源期刊
Journal of Neurogastroenterology and Motility
Journal of Neurogastroenterology and Motility GASTROENTEROLOGY & HEPATOLOGY-CLINICAL NEUROLOGY
CiteScore
6.30
自引率
8.80%
发文量
96
期刊介绍: Journal of Neurogastroenterology and Motility (J Neurogastroenterol Motil) is a joint official journal of the Korean Society of Neurogastroenterology and Motility, the Thai Neurogastroenterology and Motility Society, the Japanese Society of Neurogastroenterology and Motility, the Indian Motility and Functional Disease Association, the Chinese Society of Gastrointestinal Motility, the South East Asia Gastro-Neuro Motility Association, the Taiwan Neurogastroenterology and Motility Society and the Asian Neurogastroenterology and Motility Association, launched in January 2010 after the title change from the Korean Journal of Neurogastroenterology and Motility, published from 1994 to 2009.
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