重症肌无力危象的危险因素:中国西南地区回顾性研究

IF 2.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Xue Lin, Hongxi Chen, Xiaofei Wang, Ziyan Shi, Rui Wang, Hongyu Zhou
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引用次数: 0

摘要

背景:重症肌无力危象(MC)是一种罕见但潜在致命的并发症,可显著恶化重症肌无力(MG)患者的预后。然而,预测MC的发生仍然具有挑战性。因此,本研究旨在确定与MC相关的潜在危险因素。方法:使用四川大学华西医院2004年1月至2023年8月MG队列数据库进行回顾性研究。结果:纳入最终分析的1150例MG患者中,128例(11.1%)至少经历过一次MC发作。确定的MC独立危险因素包括年龄(风险比[HR]: 1.02, 95%可信区间[CI]: 1.01-1.03, p <;0.001),定量MG (QMG)评分(HR: 1.04, 95% CI: 1.01-1.07, p = 0.003),诊断时美国MG基金会(MGFA)分级(HR: 3.19, 95% CI: 2.38-4.28, p <;0.001),胸腺瘤的存在(HR: 3.21, 95% CI: 2.13-4.85, p <;0.001)。相比之下,广泛性MG (p = 0.891)和抗肌肉特异性酪氨酸激酶(MuSK)抗体的存在(p = 0.107)并没有显著增加发生MC的风险。结论:年龄、QMG评分和诊断时MGFA分级所显示的疾病严重程度以及胸腺瘤的存在被确定为MG患者MC的潜在预测因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Risk Factors for Myasthenic Crisis in Patients With Myasthenia Gravis: A Retrospective Study in Southwest China

Risk Factors for Myasthenic Crisis in Patients With Myasthenia Gravis: A Retrospective Study in Southwest China

Background: Myasthenic crisis (MC) is a rare but potentially fatal complication that can significantly worsen the prognosis of patients with myasthenia gravis (MG). However, predicting the occurrence of MC remains challenging. Therefore, this study aimed to identify potential risk factors associated with MC.

Methods: A retrospective study was conducted using the MG Cohort Database at the West China Hospital of Sichuan University from January 2004 to August 2023. The multivariate Cox regression analysis was performed to determine the risk factors for MC.

Results: Among the 1150 patients with MG included in the final analysis, 128 (11.1%) experienced at least one episode of MC. Independent risk factors identified for MC included age (hazard ratio [HR]: 1.02, 95% confidence interval [CI]: 1.01–1.03, p < 0.001), quantitative MG (QMG) score (HR: 1.04, 95% CI: 1.01–1.07, p = 0.003), MG Foundation of America (MGFA) class at diagnosis (HR: 3.19, 95% CI: 2.38–4.28, p < 0.001), and the presence of thymoma (HR: 3.21, 95% CI: 2.13–4.85, p < 0.001). In contrast, generalized MG (p = 0.891) and the presence of antimuscle-specific tyrosine kinase (MuSK) antibodies (p = 0.107) did not significantly increase the risk of developing MC.

Conclusion: Age, disease severity as indicated by the QMG score and MGFA class at diagnosis, along with thymoma presence were identified as potential predictors for MC in patients diagnosed with MG.

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来源期刊
CiteScore
5.30
自引率
0.00%
发文量
274
审稿时长
3-8 weeks
期刊介绍: IJCP is a general medical journal. IJCP gives special priority to work that has international appeal. IJCP publishes: Editorials. IJCP Editorials are commissioned. [Peer reviewed at the editor''s discretion] Perspectives. Most IJCP Perspectives are commissioned. Example. [Peer reviewed at the editor''s discretion] Study design and interpretation. Example. [Always peer reviewed] Original data from clinical investigations. In particular: Primary research papers from RCTs, observational studies, epidemiological studies; pre-specified sub-analyses; pooled analyses. [Always peer reviewed] Meta-analyses. [Always peer reviewed] Systematic reviews. From October 2009, special priority will be given to systematic reviews. [Always peer reviewed] Non-systematic/narrative reviews. From October 2009, reviews that are not systematic will be considered only if they include a discrete Methods section that must explicitly describe the authors'' approach. Special priority will, however, be given to systematic reviews. [Always peer reviewed] ''How to…'' papers. Example. [Always peer reviewed] Consensus statements. [Always peer reviewed] Short reports. [Always peer reviewed] Letters. [Peer reviewed at the editor''s discretion] International scope IJCP publishes work from investigators globally. Around 30% of IJCP articles list an author from the UK. Around 30% of IJCP articles list an author from the USA or Canada. Around 45% of IJCP articles list an author from a European country that is not the UK. Around 15% of articles published in IJCP list an author from a country in the Asia-Pacific region.
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