Guevara Myriam, Ng Bernard
Section of Rheumatology, Department of Medicine, Louisiana State University Health Sciences Center, New Orleans, LA, USA.
Section of Rheumatology, VA Puget Sound Healthcare System, Seattle, WA, USA;Division of Rheumatology, Department of Medicine, University of Washington, Seattle, WA, USA.
Eur J Rheumatol. 2021 Apr;8(2):62-66. doi: 10.5152/eurjrheum.2020.20193.
Despite remarkable improvements in rheumatoid arthritis (RA) treatment, there is evidence indicating that the mortality gap between patients with RA and the general population is not closing. The increase in mortality rates in patients with RA is predominantly due to cardiovascular disease (CVD). Literature suggests that important links exist between RA inflammation and atherosclerosis in CVD. Dyslipidemia is a well-known risk factor of atherosclerosis. Previous studies have suggested that antimalarials, chloroquine diphosphate, and hydroxychloroquine (HCQ), used in the treatment of autoimmune diseases, have a beneficial effect on the lipid levels. However, the studies had small sample sizes. We analyzed a Veterans Affair RA cohort of 2,925 patients to characterize the effect of 4 months' use of HCQ on the lipid levels.
Data for this cohort were obtained from the department of Veterans Affairs administrative database. Individuals (age ≥18 years) with a diagnosis of RA (ICD-9 code) at 2 or more outpatient visits from 1999 to 2009 were identified. Only the patients with at least 1 lipid level measured at 120-180 days before staring HCQ were included. Lipids levels on pre- and poststart dates of HCQ (120-180 days) were compared using student's t-test and adjusted for age, sex, race, C-reactive protein (CRP), and statin use with multivariable regression (analysis of variance/analysis of covariance) for the change in different lipid levels. To give equal weightage to covariables, we conducted an analysis of marginal means for race in each lipid level. All analyses were performed using STATA 11.
After adjusting for sex, age, race, statin use, and post CRP values >10 mg/dL using a linear regression, the factor driving the change in the different lipid levels was race (p values for total cholesterol, 0.006; low-density lipoprotein, 0.09; non-high-density lipoprotein [HDL], 0.03; atherogenic index, 0.08; and HDL, 0.17). When considering race individually using marginal means analysis, the race in the subgroup "others" was more influential.
Our results suggest that sex and race influences the HCQ effect on the lipid profiles in patients with RA. Use of HCQ in males is found to be associated with positive changes in the lipid profiles independent from the use of statins. There is a suggestion that whites and African Americans might be less susceptible to HCQ effect on lipid profiles than other races.
尽管类风湿关节炎(RA)的治疗有了显著改善,但有证据表明,RA患者与普通人群之间的死亡率差距并未缩小。RA患者死亡率上升主要归因于心血管疾病(CVD)。文献表明,RA炎症与CVD中的动脉粥样硬化之间存在重要联系。血脂异常是动脉粥样硬化的一个众所周知的危险因素。先前的研究表明,用于治疗自身免疫性疾病的抗疟药、磷酸氯喹和羟氯喹(HCQ)对血脂水平有有益影响。然而,这些研究的样本量较小。我们分析了一个由2925名患者组成的退伍军人事务RA队列,以确定使用4个月HCQ对血脂水平的影响。
该队列的数据来自退伍军人事务部行政数据库。确定了在1999年至2009年期间至少有2次门诊就诊诊断为RA(ICD-9编码)的个体(年龄≥18岁)。仅纳入在开始使用HCQ前120 - 180天至少测量过1次血脂水平的患者。使用学生t检验比较HCQ开始使用前后(120 - 180天)的血脂水平,并通过多变量回归(方差分析/协方差分析)对年龄、性别、种族、C反应蛋白(CRP)和他汀类药物使用情况进行调整,以分析不同血脂水平的变化。为了对协变量给予同等权重,我们对每个血脂水平的种族进行了边际均值分析。所有分析均使用STATA 11进行。
在使用线性回归对性别、年龄、种族、他汀类药物使用情况以及CRP值>10 mg/dL进行调整后,驱动不同血脂水平变化的因素是种族(总胆固醇的p值为0.006;低密度脂蛋白为0.09;非高密度脂蛋白[HDL]为0.03;致动脉粥样硬化指数为0.08;HDL为0.17)。当使用边际均值分析单独考虑种族时,“其他”亚组中的种族影响更大。
我们的结果表明,性别和种族会影响HCQ对RA患者血脂谱的作用。发现男性使用HCQ与血脂谱的积极变化相关,且独立于他汀类药物的使用。有迹象表明,白人和非裔美国人可能比其他种族对HCQ对血脂谱的影响更不敏感。