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多系统萎缩病理学与原发性干燥综合征有关。

Multiple system atrophy pathology is associated with primary Sjögren's syndrome.

机构信息

Department of Pathology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.

Department of Pathology, Homer Stryker M.D. School of Medicine, Western Michigan University, Kalamazoo, Michigan, USA.

出版信息

JCI Insight. 2020 Aug 6;5(15):138619. doi: 10.1172/jci.insight.138619.

Abstract

BACKGROUNDOur objective was to investigate whether primary Sjögren's syndrome (pSS) is associated with multiple system atrophy (MSA).METHODSWe performed a retrospective cohort study assessing (a) rates of MSA in a cohort of patients with pSS and (b) rates of pSS in a cohort of patients with MSA. These data were compared with rates in respective control groups. We additionally reviewed the neuropathologic findings in 2 patients with pSS, cerebellar degeneration, parkinsonism, and autonomic dysfunction.RESULTSOur cohort of 308 patients with pSS had a greater incidence of MSA compared with 4 large population-based studies and had a significantly higher prevalence of at least probable MSA (1% vs. 0%, P = 0.02) compared with 776 patients in a control cohort of patients with other autoimmune disorders. Our cohort of 26 autopsy-proven patients with MSA had a significantly higher prevalence of pSS compared with a cohort of 115 patients with other autopsy-proven neurodegenerative disorders (8% vs. 0%, P = 0.03). The 2 patients we described with pSS and progressive neurodegenerative disease showed classic MSA pathology at autopsy.CONCLUSIONOur findings provide evidence for an association between MSA and pSS that is specific to both pSS, among autoimmune disorders, and MSA, among neurodegenerative disorders. The 2 cases we describe of autopsy-proven MSA support that MSA pathology can explain neurologic disease in a subset of patients with pSS. These findings together support the hypothesis that systemic autoimmune disease plays a role in neurodegeneration.FUNDINGThe Michigan Brain Bank is supported in part through NIH grant P30AG053760.

摘要

背景

本研究旨在探究原发性干燥综合征(pSS)是否与多系统萎缩(MSA)相关。

方法

我们进行了一项回顾性队列研究,评估了(a)pSS 患者队列中 MSA 的发生率,以及(b)MSA 患者队列中 pSS 的发生率。将这些数据与各自对照组的发生率进行比较。我们还回顾了 2 例具有 pSS、小脑变性、帕金森病和自主神经功能障碍的患者的神经病理学发现。

结果

我们的 308 例 pSS 患者队列中 MSA 的发病率高于 4 项大型基于人群的研究,并且与其他自身免疫性疾病患者的 776 例对照组相比,至少可能的 MSA 患病率显著更高(1% vs. 0%,P=0.02)。我们的 26 例经尸检证实的 MSA 患者队列中 pSS 的患病率明显高于 115 例其他经尸检证实的神经退行性疾病患者队列(8% vs. 0%,P=0.03)。我们描述的 2 例具有 pSS 和进行性神经退行性疾病的患者在尸检中表现出典型的 MSA 病理学。

结论

我们的研究结果提供了证据表明 MSA 和 pSS 之间存在关联,这种关联在 pSS 与自身免疫性疾病以及 MSA 与神经退行性疾病之间均具有特异性。我们描述的 2 例经尸检证实的 MSA 病例支持 MSA 病理学可以解释一部分 pSS 患者的神经疾病。这些发现共同支持了全身性自身免疫性疾病在神经退行性变中起作用的假说。

资金

密歇根脑库部分得到 NIH 授予 P30AG053760 的支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c076/7455075/c9c584e06b83/jciinsight-5-138619-g183.jpg

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