Karp Igor, Abrahamowicz Michal, Fortin Paul R, Pilote Louise, Neville Carolyn, Pineau Christian A, Esdaile John M
University of Montreal, the Montreal University Health Center, and McGill University, Montreal, Quebec, Canada.
Arthritis Rheum. 2008 Feb 15;59(2):169-75. doi: 10.1002/art.23352.
Systemic lupus erythematosus (SLE) is characterized by a markedly elevated risk for coronary heart disease (CHD), the exact pathogenesis of which is unknown. In particular, the causal roles of corticosteroid therapy and SLE disease activity, and whether their putative effects are mediated through conventional risk factors, remain unclear.
Data abstracted retrospectively from the charts at 11,359 clinic visits for 310 patients with SLE to the Montreal General Hospital were used to investigate the associations of recent corticosteroid dose and recent Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) score with 8 CHD risk factors (total serum cholesterol, high-density lipoprotein [HDL] cholesterol, low-density lipoprotein cholesterol, apolipoprotein B [Apo B], triglycerides, systolic blood pressure [BP], body mass index, and blood glucose) and the aggregate estimate of 2-year CHD risk. Separate multivariable linear regression models estimated the mutually-adjusted effects of average daily corticosteroid dose and average SLEDAI score within the past year on the current level of each risk factor while adjusting for age, sex, cumulative damage score, disease duration, and, where appropriate, use of relevant medications.
Higher past-year corticosteroid dose was independently associated with significantly higher overall 2-year CHD risk and with higher levels of all 8 individual risk factors. Higher past-year lupus disease activity was independently associated with higher overall 2-year CHD risk, lower HDL cholesterol, and higher values of systolic BP, Apo B, triglycerides, and blood glucose.
In SLE, both recent use of corticosteroids and recent lupus activity are independently associated with higher values of several well-recognized CHD risk factors and overall 2-year CHD risk.
系统性红斑狼疮(SLE)的特征是冠心病(CHD)风险显著升高,其确切发病机制尚不清楚。特别是,皮质类固醇治疗和SLE疾病活动的因果作用,以及它们的假定作用是否通过传统风险因素介导,仍不明确。
回顾性提取蒙特利尔总医院310例SLE患者11359次门诊病历数据,以研究近期皮质类固醇剂量和近期系统性红斑狼疮疾病活动指数(SLEDAI)评分与8种CHD风险因素(总血清胆固醇、高密度脂蛋白[HDL]胆固醇、低密度脂蛋白胆固醇、载脂蛋白B[Apo B]、甘油三酯、收缩压[BP]、体重指数和血糖)以及2年CHD风险的总体估计值之间的关联。单独的多变量线性回归模型估计了过去一年中平均每日皮质类固醇剂量和平均SLEDAI评分对当前各风险因素水平的相互调整效应,同时调整了年龄、性别、累积损伤评分、疾病持续时间以及在适当情况下使用的相关药物。
过去一年较高的皮质类固醇剂量与显著较高的总体2年CHD风险以及所有8种个体风险因素的较高水平独立相关。过去一年较高的狼疮疾病活动与较高的总体2年CHD风险、较低的HDL胆固醇以及收缩压、Apo B、甘油三酯和血糖的较高值独立相关。
在SLE中,近期使用皮质类固醇和近期狼疮活动均与几种公认的CHD风险因素的较高值以及总体2年CHD风险独立相关。