Suppr超能文献

日本获得性自身免疫性自主神经功能障碍儿童和青少年中的 gAChR 抗体。

gAChR antibodies in children and adolescents with acquired autoimmune dysautonomia in Japan.

机构信息

Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.

Department of Pediatrics, Tokyo Metropolitan Ohtsuka Hospital, Tokyo, Japan.

出版信息

Ann Clin Transl Neurol. 2021 Apr;8(4):790-799. doi: 10.1002/acn3.51317. Epub 2021 Feb 23.

Abstract

OBJECTIVE

Patients with acquired autonomic dysfunction may have antibodies specific to the ganglionic nicotinic acetylcholine receptor (gAChR). However, the clinical features of children and adolescents with acquired autonomic dysfunction (AAD) remain unclear. This study aimed to determine the clinical features of pediatric patients with acquired autonomic dysfunction.

METHODS

This study retrospectively examined a series of patients of AAD with serum gAChR antibodies who were referred to our laboratory for antibody testing between January 2012 and April 2019. The study included 200 patients (<20 years, 20 cases; ≥20 years, 175 cases) with clinical features of AAD.

RESULTS

Upon comparing pediatric and adult patients, we found that antecedent infection and autonomic symptoms at onset with gastrointestinal symptoms occurred more frequently in children with AAD. We confirmed that four children (20.0%) met the diagnostic criteria for postural orthostatic tachycardia syndrome (POTS). A significantly higher number of children than adults had POTS (P = 0.002). In addition, upper GI dysfunction was more prevalent in children than in adults (P = 0.042). In particular, nausea and vomiting occurred in 60.0% of children with AAD and in 21.1% of adults (P < 0.001). The frequency of paralytic ileus was significantly higher in children with AAD (20.0%) relative to adults (6.3%) (P = 0.030). Regarding extra-autonomic manifestations, encephalopathy was more frequent in children (15.0%) than in adults (1.1%) (P < 0.001).

INTERPRETATION

Pediatric AAD patients have their own clinical characteristics, and these features may be unique to children and adolescents.

摘要

目的

获得性自主神经功能障碍患者可能具有针对神经节烟碱型乙酰胆碱受体(gAChR)的特异性抗体。然而,儿童和青少年获得性自主神经功能障碍(AAD)的临床特征尚不清楚。本研究旨在确定获得性自主神经功能障碍患儿的临床特征。

方法

本研究回顾性分析了 2012 年 1 月至 2019 年 4 月期间因抗体检测而被转至我院实验室的一系列 AAD 血清 gAChR 抗体阳性患者。该研究纳入了 200 例(<20 岁 20 例;≥20 岁 175 例)有 AAD 临床特征的患者。

结果

在比较儿科和成年患者时,我们发现 AAD 患儿前驱感染和发病时的自主神经症状以及胃肠道症状更为常见。我们证实有 4 名儿童(20.0%)符合体位性心动过速综合征(POTS)的诊断标准。患有 POTS 的儿童明显多于成年人(P=0.002)。此外,上消化道功能障碍在儿童中比在成人中更为常见(P=0.042)。特别是,AAD 患儿中有 60.0%出现恶心和呕吐,而成人仅为 21.1%(P<0.001)。AAD 患儿麻痹性肠梗阻的发生率明显高于成人(20.0%对 6.3%)(P=0.030)。关于非自主神经表现,脑病在儿童中更为常见(15.0%),而成人仅为 1.1%(P<0.001)。

结论

儿科 AAD 患者具有自身的临床特征,这些特征可能是儿童和青少年所特有的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50dc/8045944/0c8b9f89e298/ACN3-8-790-g002.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验