Ng R, Bernatsky S, Rahme E
1 Research Institute of the McGill University Health Centre, Medicine, Montreal, Canada.
2 Divisions of Rheumatology and Clinical Epidemiology, McGill University Health Centre, Medicine - Rheumatology, Montreal, Canada.
Lupus. 2017 Aug;26(9):1005-1011. doi: 10.1177/0961203317692435. Epub 2017 Feb 8.
Objective Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by an array of organ manifestations that can appear during flares and disappear during remissions. The objectives of this study were: (i) to examine SLE manifestation groups longitudinally in an SLE cohort; and (ii) to assess the association between early antimalarial treatment and renal manifestations. Methods Seven SLE manifestation groups-cutaneous, hematologic, lung, musculoskeletal, neuropsychiatric, serositis, renal-were tracked using Kaplan-Meier survival curves in an incident SLE cohort from Quebec health administrative data ( n = 2010). A subgroup with provincial drug insurance coverage was followed over time to examine the association between early antimalarial treatment (within three months after SLE diagnosis) and renal manifestations using a Cox proportional hazards survival model. Results Cutaneous manifestations was the most common manifestation at SLE diagnosis (30.0%, 95% CI: 27.7-32.2%). About two-thirds (66.2%, 95% CI: 63.4-68.9%) of patients had evidence of at least one SLE manifestation at diagnosis, which increased to 87.2% (95% CI: 84.2-90.3%) by the end of follow-up. After adjusting for age, sex, early concomitant systemic steroid therapy, Charlson comorbidity index, primary care visits in the year prior and other SLE manifestations at baseline, no statistically significant association was established between antimalarial therapy and renal manifestations. Conclusion This study provides insight regarding organ manifestations within a population-based sample. Most patients identified with SLE had other diagnostic evidence that supports an underlying diagnosis of SLE. No protective effects for antimalarial agents against renal manifestations could be established in this population-based cohort.
目的 系统性红斑狼疮(SLE)是一种自身免疫性疾病,其特征是一系列器官表现可在病情发作时出现,缓解期消失。本研究的目的是:(i)在一个SLE队列中纵向检查SLE表现组;(ii)评估早期抗疟治疗与肾脏表现之间的关联。方法 利用魁北克卫生行政数据中的一个新发SLE队列(n = 2010),采用Kaplan-Meier生存曲线追踪7个SLE表现组——皮肤、血液学、肺部、肌肉骨骼、神经精神、浆膜炎、肾脏。对有省级药物保险覆盖的亚组进行随访,使用Cox比例风险生存模型检查早期抗疟治疗(SLE诊断后三个月内)与肾脏表现之间的关联。结果 皮肤表现是SLE诊断时最常见的表现(30.0%,95%CI:27.7 - 32.2%)。约三分之二(66.2%,95%CI:63.4 - 68.9%)的患者在诊断时有至少一种SLE表现的证据,到随访结束时这一比例增至87.2%(95%CI:84.2 - 90.3%)。在调整年龄、性别、早期同时使用全身性激素治疗、Charlson合并症指数、前一年的初级保健就诊次数以及基线时的其他SLE表现后,抗疟治疗与肾脏表现之间未建立统计学上的显著关联。结论 本研究为基于人群的样本中的器官表现提供了见解。大多数确诊为SLE的患者有其他诊断证据支持SLE的潜在诊断。在这个基于人群的队列中,无法确定抗疟药对肾脏表现的保护作用。