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由于直立性心动过速综合征,嗜酸性粒细胞性胃肠病患者自主神经功能障碍的患病率增加。

Increased prevalence of autonomic dysfunction due to postural orthostatic tachycardia syndrome in patients with eosinophilic gastrointestinal disorders.

机构信息

Center for Esophageal Diseases and Swallowing, Center for Gastrointestinal Biology and Disease, Division of Gastroenterology and Hepatology, University of North Carolina School of Medicine, Chapel Hill, NC, USA.

出版信息

J Gastrointestin Liver Dis. 2019 Mar;28(1):47-51. doi: 10.15403/jgld.2014.1121.281.syd.

Abstract

BACKGROUND AND AIMS

Eosinophilic gastrointestinal disorders (EGIDs) have been linked with atopic conditions, connective tissue disorders, and autoimmunity, but the association between EGIDs and autonomic dysfunction has not been extensively described. We aimed to assess this association and determine the prevalence of autonomic dysfunction in our EGID population.

METHODS

In this retrospective cohort study, we analyzed adult patients in the University of North Carolina Eosinophilic Esophagitis (EoE)/EGID database who also had a diagnosis of comorbid autonomic dysfunction (postural orthostatic tachycardia syndrome [POTS] or gastroparesis). The electronic medical record was abstracted and disease characteristics summarized.

RESULTS

We identified seven patients who had EGID and autonomic dysfunction. All had POTS and were Caucasian, and five (71%) were female; 2 also had gastroparesis. Onset of autonomic symptoms coincided with onset of EGID symptoms in 3 patients (43%) or with an acute EGID flare in 3. In no cases did successful control of EGID lead to improvement of autonomic symptoms. Two subjects (29%) had comorbid Ehlers-Danlos syndrome and mast cell activation syndrome. The prevalence of POTS in EGID patients was 7/560 (1.25%), compared to an estimated 0.17% prevalence of POTS in the general population.

CONCLUSIONS

The prevalence of autonomic dysfunction was 5-10-fold higher in EGID than expected in the general population, suggesting an association between the two conditions, though the underlying mechanism is unclear. Providers should consider comorbid autonomic dysfunction in patients with EGID, particularly when symptoms persist despite treatment.

摘要

背景和目的

嗜酸性粒细胞性胃肠道疾病(EGIDs)与特应性疾病、结缔组织疾病和自身免疫有关,但 EGIDs 与自主神经功能障碍之间的关联尚未得到广泛描述。我们旨在评估这种关联,并确定我们的 EGID 人群中自主神经功能障碍的患病率。

方法

在这项回顾性队列研究中,我们分析了北卡罗来纳大学嗜酸性食管炎(EoE)/EGID 数据库中患有合并自主神经功能障碍(直立性心动过速综合征[POTS]或胃轻瘫)的成年患者。从电子病历中提取信息并总结疾病特征。

结果

我们确定了 7 名患有 EGID 和自主神经功能障碍的患者。所有患者均患有 POTS,均为白种人,其中 5 名(71%)为女性;2 名还患有胃轻瘫。3 名患者(43%)的自主症状与 EGID 症状同时出现,3 名患者的自主症状与急性 EGID 发作同时出现。在没有成功控制 EGID 的情况下,自主症状均未得到改善。2 名患者(29%)患有埃勒斯-当洛斯综合征和肥大细胞激活综合征。EGID 患者中 POTS 的患病率为 7/560(1.25%),而普通人群中 POTS 的患病率估计为 0.17%。

结论

EGID 患者自主神经功能障碍的患病率比普通人群高 5-10 倍,提示这两种疾病之间存在关联,但潜在机制尚不清楚。在治疗后症状仍持续存在的情况下,医生应考虑 EGID 患者合并自主神经功能障碍的可能性。

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