Suppr超能文献

中国抗 AChR-MuSK-LRP4 抗体阴性重症肌无力的临床特征。

Clinical characteristics of anti-AChR-MuSK-LRP4 antibody-negative myasthenia gravis in China.

机构信息

Department of Neurology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Department of Neuroimmunology, Henan Institute of Medical and Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, China.

出版信息

Muscle Nerve. 2023 Jun;67(6):481-488. doi: 10.1002/mus.27822. Epub 2023 Apr 3.

Abstract

INTRODUCTION/AIMS: Descriptions of the clinical characteristics of anti-AChR-MuSK-LRP4 antibody-negative myasthenia gravis (triple-negative myasthenia gravis, TNMG) are lacking in the current literature. Therefore, we investigated the clinical characteristics of TNMG in Chinese patients.

METHODS

We retrospectively analyzed 925 patients with MG registered in the Department of Neuroimmunology, Henan Institute of Medical and Pharmaceutical Sciences from January 2015 to March 2021.

RESULTS

One hundred six patients diagnosed with TNMG were included in the study. The average age of onset was 32.4 y, with a male-to-female ratio of 1:1. The age of onset showed a bimodal distribution: 0-9 y and 40-49 y. Adult patients were more likely to have weakness of limb and bulbar muscles (p < .05). Thymic hyperplasia was found in 20.2% of the patients. Younger patients were more likely to relapse. The rate of adult early-onset myasthenia gravis reaching complete stable remission and pharmacological remission was 47.6%, and the prognosis was better than that in juvenile-onset myasthenia gravis (p = .019). Older age of onset was the only risk factor for the development of generalized TNMG from ocular TNMG (R = 1.046, p = .002, 95% confidence interval 1.017-1.077).

DISCUSSION

This study showed that the clinical characteristics of patients with TNMG varied among the different age groups. Significant findings included a bimodal distribution of onset age, coexisting thymic hyperplasia, and a generally favorable prognosis.

摘要

介绍/目的:目前文献中缺乏抗 AChR-MuSK-LRP4 抗体阴性重症肌无力(三阴性重症肌无力,TNMG)的临床特征描述。因此,我们研究了中国患者 TNMG 的临床特征。

方法

我们回顾性分析了 2015 年 1 月至 2021 年 3 月在河南医学高等专科学校神经免疫科登记的 925 例 MG 患者。

结果

本研究纳入了 106 例诊断为 TNMG 的患者。发病平均年龄为 32.4 岁,男女比例为 1:1。发病年龄呈双峰分布:0-9 岁和 40-49 岁。成年患者更易出现四肢和球部肌肉无力(p<0.05)。20.2%的患者有胸腺增生。年轻患者更易复发。成年早发型 MG 完全稳定缓解和药物缓解率为 47.6%,预后优于青少年起病型 MG(p=0.019)。发病年龄较大是从眼肌型 TNMG 发展为全身型 TNMG 的唯一危险因素(R=1.046,p=0.002,95%置信区间 1.017-1.077)。

讨论

本研究表明,TNMG 患者的临床特征在不同年龄组之间存在差异。重要发现包括发病年龄双峰分布、伴发胸腺增生以及总体预后良好。

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