重症肌无力自身抗体:聚类分析及临床相关性。

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Frontiers in Neurology Pub Date : 2025-02-04 eCollection Date: 2025-01-01 DOI:10.3389/fneur.2025.1537783
Xupeng Sun, Meijie Qu, Xi Rong, Mingxing Lv, Yunbin Zhao, Yunjun Yan, Lin Liu, Na Sun, Hua Yue, Min Liu
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摘要

目的:探讨644例重症肌无力(MG)患者自身抗体簇及其与临床特征的相关性。方法:回顾664例MG患者的病历资料。选取5种自身抗体AChR、MuSK、titin、RyR、LRP4进行聚类分析。比较两组患者的临床表现。在没有事先聚类的情况下,也进行了个体自身抗体与临床表现以及不同MGFA亚型之间的单独关联分析。结果:鉴定出两个独立的自身抗体簇,临床表现有显著差异。第1组(485例)的特点是RyR-、titin-和AChR-的比例较高,第2组(179例)的特点是RyR+、titin+和AChR+的比例较高。第2组患者年龄较大,QMG评分和并发症的发生率较高,特别是高血压、糖尿病、心脑血管疾病和眼病。个体抗体分析显示,男性病例更可能是AChR+和titin+,年龄较大与AChR+、RyR+和titin+相关。在MGFA亚型中,AChR、MuSK、titin、并发症、胸腺瘤和高血压存在显著差异。随着MG严重程度从I型增加到V型,AChR+、RyR+和titin+比例在IIa期达到峰值。MuSK+患者相对少见,多出现在b亚型组。b型患者MuSK+患病率高于a型患者,心脑血管疾病发病率高于a型患者。结论:总体而言,簇2特征对患者不利。本研究为中国MG患者的临床和自身抗体谱提供了有价值的见解。
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Autoantibodies in myasthenia gravis: cluster analysis and clinical correlations.

Objective: This study aimed to explore autoantibody clusters and their correlations with clinical features in 644 myasthenia gravis (MG) patients.

Methods: Medical records of 664 MG patients were reviewed. Five autoantibodies (AChR, MuSK, titin, RyR, and LRP4) were selected for cluster analysis. The various clinical manifestations were compared between clusters. Separate association analyses between individual autoantibodies and clinical manifestations as well as among different MGFA subtypes were also performed without prior clustering.

Results: Two separate autoantibody clusters were identified, with significantly different clinical manifestations. Cluster 1 (485 patients) was characterized by higher proportions of RyR-, titin-, and AChR-, while cluster 2 (179 patients) had higher proportions of RyR+, titin+, and AChR+. Cluster 2 patients were older and had elevated QMG scores and odds of complications, particularly hypertension, diabetes, cardiovascular and cerebrovascular diseases, and eye conditions. Individual antibody analysis revealed that male cases were more likely to be AChR+ and titin+, and older age was associated with AChR+, RyR+, and titin+. Among MGFA subtypes, significant differences were detected in AChR, MuSK, titin, complications, thymoma, and hypertension. As MG severity increased from types I to V, AChR+, RyR+, and titin+ proportions peaked at stage IIa. MuSK+ patients were relatively rare and mostly present in the subtype b group. Type b patients had higher MuSK+ prevalence and increased cardiovascular and cerebrovascular disease incidence rates than type a cases.

Conclusion: Overall, cluster 2 features were less favorable to patients. This study provides valuable insights into the clinical and autoantibody profiles of Chinese MG patients.

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来源期刊
Frontiers in Neurology
Frontiers in Neurology CLINICAL NEUROLOGYNEUROSCIENCES -NEUROSCIENCES
CiteScore
4.90
自引率
8.80%
发文量
2792
审稿时长
14 weeks
期刊介绍: The section Stroke aims to quickly and accurately publish important experimental, translational and clinical studies, and reviews that contribute to the knowledge of stroke, its causes, manifestations, diagnosis, and management.
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