Kim Yeseong, Shibli Fahmi, Fu Yuhan, Song Gengqing, Fass Ronnie
Department of Internal Medicine, MetroHealth Medical Center, Case Western Reserve University, Cleveland, OH, USA.
Division of Gastroenterology and Hepatology, The Esophageal and Swallowing Center, MetroHealth Medical Center, Case Western Reserve University, Cleveland, OH, USA.
J Neurogastroenterol Motil. 2023 Oct 30;29(4):478-485. doi: 10.5056/jnm22173. Epub 2023 Aug 2.
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.
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.
Odds of MS patients developing achalasia or DES were (OR, 2.09; 95% CI, 1.73-2.52; < 0.001) and (OR, 3.15; 95% CI, 2.89-3.42; < 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.
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.
背景/目的:多发性硬化症(MS)是一种以中枢神经系统主要脱髓鞘为特征的炎症性疾病。弥漫性食管痉挛(DES)和贲门失弛缓症均为食管蠕动障碍,可导致吞咽困难的临床症状。有人提出,其机制涉及肌间神经丛节前和节后神经纤维功能障碍。我们试图确定MS是否会增加患贲门失弛缓症或DES的风险。
使用Explorys数据库进行队列分析。进行单因素逻辑回归以确定MS赋予所研究的每种动力障碍的比值比。在各队列中比较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、使用阿片类药物或患有CREST综合征的患者被排除在研究之外。
MS患者患贲门失弛缓症或DES的比值比分别为(比值比,2.09;95%置信区间,1.73 - 2.52;P < 0.001)和(比值比,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,分别有27.27%、18.18%、9.09%和45.45%的患者有尿失禁、胃轻瘫、阳痿和失眠症状。在MS/DES队列中,有这些症状的患者分别为35.19%、11.11%、3.70%和55.56%。在无动力障碍的MS患者中,有这些症状的患者分别为12.64%、0.79%、2.21%和21.85%。
与无MS的患者相比,MS患者患贲门失弛缓症或DES的几率更高。患有贲门失弛缓症或DES的MS患者自主神经功能障碍合并症的发生率更高。这表明就导致自主神经功能障碍的神经元退化和脱髓鞘程度而言,这些患者的疾病表型更严重。