National Referral Centre for Rare Autoimmune and Systemic Diseases, Hôpital Cochin, AP-HP Centre and Université Paris Cité and Centre de Recherche en Epidémiologie et Statistiques (CRESS), Unité Inserm 1153, Université de Paris Cité, Paris, France.
Biologie du médicament-Toxicologie, AP-HP Centre-Hôpital Cochin, Université Paris Cité, and UMR8038 CNRS, U1268 INSERM, Université Paris Cité, PRES Sorbonne Paris Cité, CARPEM, Paris, France.
Arthritis Rheumatol. 2023 Dec;75(12):2195-2206. doi: 10.1002/art.42645. Epub 2023 Nov 13.
The goals of this study were to assess the associations of severe nonadherence to hydroxychloroquine (HCQ), objectively assessed by HCQ serum levels, and risks of systemic lupus erythematosus (SLE) flares, damage, and mortality rates over five years of follow-up.
The Systemic Lupus International Collaborating Clinics (SLICC) Inception Cohort is an international multicenter initiative (33 centers throughout 11 countries). The serum of patients prescribed HCQ for at least three months at enrollment were analyzed. Severe nonadherence was defined by a serum HCQ level <106 ng/mL or <53 ng/mL for HCQ doses of 400 or 200 mg/day, respectively. Associations with the risk of a flare (defined as a Systemic Lupus Erythematosus Disease Activity Index 2000 increase ≥4 points, initiation of prednisone or immunosuppressive drugs, or new renal involvement) were studied with logistic regression, and associations with damage (first SLICC/American College of Rheumatology Damage Index [SDI] increase ≥1 point) and mortality with separate Cox proportional hazard models.
Of the 1,849 cohort participants, 660 patients (88% women) were included. Median (interquartile range) serum HCQ was 388 ng/mL (244-566); 48 patients (7.3%) had severe HCQ nonadherence. No covariates were clearly associated with severe nonadherence, which was, however, independently associated with both flare (odds ratio 3.38; 95% confidence interval [CI] 1.80-6.42) and an increase in the SDI within each of the first three years (hazard ratio [HR] 1.92 at three years; 95% CI 1.05-3.50). Eleven patients died within five years, including 3 with severe nonadherence (crude HR 5.41; 95% CI 1.43-20.39).
Severe nonadherence was independently associated with the risks of an SLE flare in the following year, early damage, and five-year mortality.
本研究旨在评估羟氯喹(HCQ)严重不依从与系统性红斑狼疮(SLE)发作、损伤和五年内死亡率风险之间的关联,严重不依从通过 HCQ 血清水平客观评估。
系统性红斑狼疮国际合作临床研究(SLICC)起始队列是一项国际性多中心倡议(来自 11 个国家的 33 个中心)。入组时至少服用 HCQ 三个月的患者的血清进行分析。严重不依从定义为血清 HCQ 水平<106ng/ml(400mg/天剂量时)或<53ng/ml(200mg/天剂量时)。使用逻辑回归研究与发作风险的关联(定义为系统性红斑狼疮疾病活动指数 2000 增加≥4 分、开始使用泼尼松或免疫抑制剂或新的肾脏受累),使用单独的 Cox 比例风险模型研究与损伤(第一个 SLICC/美国风湿病学会损伤指数[SDI]增加≥1 分)和死亡率的关联。
在 1849 名队列参与者中,纳入了 660 名患者(88%为女性)。中位(四分位间距)血清 HCQ 为 388ng/ml(244-566);48 名患者(7.3%)存在严重的 HCQ 不依从。没有明确的协变量与严重不依从相关,但严重不依从与发作(比值比 3.38;95%置信区间[CI]1.80-6.42)和前三年每个 SDI 的增加(3 年时 HR 1.92;95%CI1.05-3.50)均独立相关。五年内 11 名患者死亡,其中 3 名严重不依从(粗 HR 5.41;95%CI1.43-20.39)。
严重不依从与 SLE 发作、早期损伤和五年死亡率风险独立相关。