Institute of Medicine, School of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Division of Cardiology, Department of Internal Medicine, Chung-Shan Medical University Hospital, Taichung, Taiwan.
Front Immunol. 2021 Apr 2;12:631869. doi: 10.3389/fimmu.2021.631869. eCollection 2021.
Hydroxychloroquine (HCQ) is widely used to treat rheumatic diseases including rheumatoid arthritis (RA), systemic lupus erythematosus (SLE) and Sjögren's syndrome (SS). Cardiac arrhythmia has been concerned as important safety issue for HCQ. The aim of this study was to investigate whether hydroxychloroquine increases new-onset arrhythmia among patients with RA, SLE or SS.
This was a retrospective cohort study that conducted from the longitudinal health insurance database of Taiwan. Patients with newly diagnosed RA, SLE or SS with age ≥20 years old were selected from 2000 to 2012. Patients who received HCQ and without HCQ treatment groups were matched by propensity score to minimize the effect of selection bias and confounders. The Cox proportional hazard model was used to analyze the risk of arrhythmia between the two groups after controlling for related variables.
A total of 15892 patients were selected to participate and finally 3575 patients were enrolled in each group after matching. There was no different risk of all arrhythmia in patients using HCQ than without HCQ (adjusted hazards ratio 0.81, 95% CI 0.61-1.07) and ventricular arrhythmia as well. The incidence of arrhythmia did not increase when HCQ co-administrated with macrolides. The arrhythmia risk was also not different regardless of daily HCQ dose <400mg or ≥400mg or follow-up duration of ≦4 months or >4 months.
The administration of HCQ did not increase the risk of all cardiac arrhythmia and ventricular arrhythmia regardless of different duration of treatment (≦4 months or >4 months) or cumulative dose (<400mg or ≥400mg) in patients with common autoimmune diseases such as RA, SLE and SS.
羟氯喹(HCQ)广泛用于治疗风湿性疾病,包括类风湿关节炎(RA)、系统性红斑狼疮(SLE)和干燥综合征(SS)。心律失常已被认为是 HCQ 的一个重要安全问题。本研究旨在探讨 HCQ 是否会增加 RA、SLE 或 SS 患者新发心律失常的风险。
这是一项回顾性队列研究,在台湾的纵向健康保险数据库中进行。从 2000 年至 2012 年,选择年龄≥20 岁、新诊断为 RA、SLE 或 SS 的患者。通过倾向评分匹配接受 HCQ 和未接受 HCQ 治疗的患者,以最小化选择偏差和混杂因素的影响。在控制相关变量后,采用 Cox 比例风险模型分析两组心律失常的风险。
共选择了 15892 名患者参与,最终匹配后每组有 3575 名患者入组。与未使用 HCQ 的患者相比,使用 HCQ 的患者发生所有心律失常(调整后的危险比 0.81,95%CI 0.61-1.07)和室性心律失常的风险无差异。当 HCQ 与大环内酯类药物联合使用时,心律失常的发生率并没有增加。无论 HCQ 的日剂量<400mg 或≥400mg 或随访时间≦4 个月或>4 个月,心律失常的风险也没有差异。
在 RA、SLE 和 SS 等常见自身免疫性疾病患者中,无论治疗时间(≦4 个月或>4 个月)或累积剂量(<400mg 或≥400mg)长短不同,HCQ 的使用并未增加所有心律失常和室性心律失常的风险。