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干燥综合征相关免疫反应性自主神经病:病例系列及文献复习。

Immunoresponsive Autonomic Neuropathy in Sjögren Syndrome-Case Series and Literature Review.

出版信息

Am J Ther. 2019 Jan/Feb;26(1):e66-e71. doi: 10.1097/MJT.0000000000000583.

Abstract

BACKGROUND

Sjögren syndrome (SS) is one of the most common autoimmune disorders that classically affects exocrine glands, resulting in keratoconjunctivitis sicca and xerostomia, and frequently is associated with other systemic symptoms. SS appears to have a particular predilection for involving the autonomic nervous system.

STUDY QUESTION

Does immunotherapy improve signs and symptoms of autonomic nervous system impairment in SS?

STUDY DESIGN

This is a retrospective review of patients seen in the autonomic clinic at our institution who underwent an evaluation for a suspected autonomic disorder that ultimately was attributed to SS. SS patients who were treated with immunotherapy and completed autonomic testing before and after treatment were included in this review.

RESULTS

A total of 4 patients were identified who were treated for SS-related autonomic dysfunction with immunotherapy and underwent repeat autonomic testing after treatment. Marked clinical and functional improvement was seen after treatment with intravenous immunoglobulin in all patients and adjunctive rituximab therapy in 1 patient. The clinical improvement with immunotherapy in these patients correlated with markedly improved findings on autonomic testing in all.

MEASURES AND OUTCOMES

Clinical symptoms and results of autonomic testing prior to and following immunotherapy were assessed.

CONCLUSIONS

Autonomic signs and symptoms in SS are potentially immunoresponsive, but immunotherapy in these patients may require repeated, ongoing, or adjunctive therapy for optimal and sustained improvement.

摘要

背景

干燥综合征(SS)是最常见的自身免疫性疾病之一,经典地影响外分泌腺,导致干眼症和口干症,并且经常与其他全身症状相关。SS 似乎对自主神经系统有特殊的倾向。

研究问题

免疫疗法是否能改善 SS 患者自主神经系统损伤的症状和体征?

研究设计

这是对在我们机构自主神经诊所就诊的患者进行的回顾性研究,这些患者因疑似自主神经紊乱而接受评估,最终被归因于 SS。接受免疫治疗且在治疗前后完成自主神经测试的 SS 患者被纳入本研究。

结果

共确定了 4 名患者,他们因 SS 相关自主神经功能障碍接受免疫治疗,并在治疗后接受重复自主神经测试。所有患者在接受静脉注射免疫球蛋白治疗后均出现明显的临床和功能改善,1 例患者接受辅助利妥昔单抗治疗。这些患者的免疫治疗临床改善与自主神经测试的明显改善相关。

措施和结果

评估了免疫治疗前后的临床症状和自主神经测试结果。

结论

SS 中的自主神经症状是潜在的免疫反应性的,但这些患者的免疫疗法可能需要重复、持续或辅助治疗以获得最佳和持续的改善。

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