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免疫抑制对眼肌型重症肌无力发生全身症状风险的影响:一项回顾性队列研究。

Effect of Immunosuppression in Risk of Developing Generalized Symptoms in Ocular Myasthenia Gravis: A Retrospective Cohort Study.

机构信息

From the Department of Neurology (D.M.), National Institute of Mental Health and Neuro Sciences, Bangalore, India; Prosserman Centre for Neuromuscular Disease (D.M., M.A., H.D.K., V.B., M.G.M., C.B.-T.), Toronto General Hospital, University Health Network; and Institute of Health Policy (C.B.-T.), Management and Evaluation, University of Toronto, Ontario, Canada.

出版信息

Neurology. 2024 Aug 27;103(4):e209722. doi: 10.1212/WNL.0000000000209722. Epub 2024 Jul 30.

Abstract

BACKGROUNDS AND OBJECTIVES

Early use of immunosuppression has been suggested to prevent generalization of ocular myasthenia gravis (OMG), but high-quality evidence is limited in this regard. We examined whether treatment with prednisone and other immunosuppressants reduce the risk of generalization in OMG.

METHODS

This is a retrospective study of consecutive adults with pure OMG who had a minimum 6 months of follow-up. The main outcome was the time to developing generalized symptoms. We used propensity scores to create matched data sets of patients treated with prednisone or any immunosuppressant vs controls. We also used unmatched models with inverse probability of treatment weights (IPTW) and variable exposure times. We used Cox proportional hazards model to estimate hazard ratio (HR) for generalization, comparing treated patients vs controls.

RESULTS

A total of 154 patients were included, with a mean follow-up of 87.4 ± 73 months since onset. Forty-three (28%) were generalized, and mean time to generalization from diagnosis was 24.2 ± 24.1 months. Patients who received prednisone had lower risk of generalization than controls, with pooled HR 0.43 (95% CI 0.19-1.06) for the matched model, HR 0.46 (95% CI 0.21-0.89) for the IPTW model, and for HR 0.44 (95% CI 0.23-0.81) for the time-dependent exposure model. Patients who received any immunosuppressant had lower risk of generalization, with HR 0.30 (95% CI 0.11-0.77), 0.32 (95% CI 0.14-0.70), and 0.35 (95% CI 0.15-0.80) for the matched, IPTW, and IPTW-varying exposure models, respectively.

DISCUSSION

Our study provides evidence that steroidal and nonsteroidal immunosuppression in patients with OMG is associated with a reduced risk of developing generalized symptoms over time. This supports the early use of immunosuppression in this population.

CLASSIFICATION OF EVIDENCE

This study provides Class III evidence that treatment of OMG with corticosteroids or nonsteroidal immunosuppressants reduces the risk of generalization.

摘要

背景和目的

早期使用免疫抑制治疗被认为可以预防眼肌型重症肌无力(OMG)的全身性发展,但这方面的高质量证据有限。我们研究了泼尼松和其他免疫抑制剂的治疗是否可以降低 OMG 患者全身性发展的风险。

方法

这是一项连续纳入成年纯 OMG 患者的回顾性研究,患者的随访时间至少为 6 个月。主要结局是出现全身症状的时间。我们使用倾向评分创建了接受泼尼松或任何免疫抑制剂治疗的患者与对照组的匹配数据集。我们还使用了无匹配的逆概率治疗权重(IPT)和可变暴露时间模型。我们使用 Cox 比例风险模型来估计全身性发展的风险比(HR),比较治疗组和对照组。

结果

共纳入 154 例患者,自发病以来的平均随访时间为 87.4 ± 73 个月。43 例(28%)发生全身性发展,从诊断到全身性发展的平均时间为 24.2 ± 24.1 个月。接受泼尼松治疗的患者发生全身性发展的风险低于对照组,匹配模型的汇总 HR 为 0.43(95%CI 0.19-1.06),IPT 模型的 HR 为 0.46(95%CI 0.21-0.89),时间依赖的暴露模型的 HR 为 0.44(95%CI 0.23-0.81)。接受任何免疫抑制剂治疗的患者发生全身性发展的风险较低,匹配模型、IPT 模型和 IPT 随时间变化的暴露模型的 HR 分别为 0.30(95%CI 0.11-0.77)、0.32(95%CI 0.14-0.70)和 0.35(95%CI 0.15-0.80)。

讨论

我们的研究提供了证据表明,在 OMG 患者中使用类固醇和非类固醇免疫抑制剂与随着时间的推移发展为全身症状的风险降低相关。这支持在该人群中早期使用免疫抑制治疗。

分类证据

本研究提供了 III 级证据,表明治疗 OMG 时使用皮质类固醇或非甾体免疫抑制剂可降低全身性发展的风险。

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