Bastian H M, Alarcón G S, Roseman J M, McGwin G, Vilá L M, Fessler B J, Reveille J D
Department of Medicine, Division of Clinical Immunology and Rheumatology, The University of Alabama, Birmingham, USA.
Rheumatology (Oxford). 2007 Apr;46(4):683-9. doi: 10.1093/rheumatology/kel347. Epub 2006 Nov 28.
To determine the factors predictive of new or worsening proteinuria in a large multiethnic cohort of patients with systemic lupus erythematosus (SLE).
Five hundred and twenty-nine SLE patients from a multiethnic US cohort [LUpus in MInorities: NAture versus Nurture (LUMINA)] were evaluated for new or worsening proteinuria using the categories of the Systemic Lupus Activity Measure-Revised: (1), normal; (2), trace or 1+ proteinuria on the dipstick; (3), 2-3+ proteinuria and (4), > or =4+ proteinuria. A rise in urinary protein was considered a positive event visit. Basic demographic and socioeconomic variables were assessed at baseline (T0). Clinical and immunological variables including disease features, activity, duration, comorbidities (such as hypertension and diabetes), medications and autoantibodies were assessed at the visit preceding a positive event visit. Selected HLA-DR and HLA-DQ alleles, and FCGR receptor polymorphisms were assessed. Data were analysed using logistic regression analyses and generalized estimating equations.
There were 243 patients (59.1% of 93 Texan Hispanics, 37.0% of 100 Puerto Rican Hispanics, 58.0% of 181 African Americans and 29.7% of 155 Caucasians) with new or worsening proteinuria, and 364 positive events in 2801 visits. Younger age [Odds ratio (OR) = 1.013, 95% confidence limits (CL) = 1.001-1.024, P < 0.0334], anti-dsDNA (OR = 1.554, CL = 1.149-2.100, P < 0.0042), and HLA-DRB1*1503 (OR = 1.746, 95% CL = 1.573-2.2673, P < 0.0103) were found to independently predict the occurrence of new or worsening proteinuria.
The factors predictive of new or worsening proteinuria include traditional factors associated with lupus nephritis, such as age and anti-dsDNA, as well as HLA-DRB1*1503, which has not been previously described in association with lupus nephritis, new or worsening proteinuria.
确定在一个大型多民族系统性红斑狼疮(SLE)患者队列中预测新发或蛋白尿恶化的因素。
对来自美国一个多民族队列[少数族裔狼疮:先天与后天(LUMINA)]的529例SLE患者,使用系统性狼疮活动度测量修订版的分类评估新发或蛋白尿恶化情况:(1)正常;(2)尿试纸检测微量或1+蛋白尿;(3)2 - 3+蛋白尿;(4)≥4+蛋白尿。尿蛋白升高被视为阳性事件访视。在基线(T0)评估基本人口统计学和社会经济变量。在阳性事件访视前的那次访视评估临床和免疫学变量,包括疾病特征、活动度、病程、合并症(如高血压和糖尿病)、用药情况和自身抗体。评估选定的HLA - DR和HLA - DQ等位基因以及FCGR受体多态性。使用逻辑回归分析和广义估计方程分析数据。
有243例患者(93例德克萨斯西班牙裔中的59.1%,100例波多黎各西班牙裔中的37.0%,181例非裔美国人中的58.0%,155例白种人中的29.7%)出现新发或蛋白尿恶化,在2801次访视中有364次阳性事件。发现年龄较小[比值比(OR)=1.013,95%置信区间(CL)=1.001 - 1.024,P<0.0334]、抗双链DNA(OR = 1.554,CL = 1.149 - 2.100,P<0.0042)和HLA - DRB1*1503(OR = 1.746,95%CL = 1.573 - 2.2673,P<0.0103)可独立预测新发或蛋白尿恶化的发生。
预测新发或蛋白尿恶化的因素包括与狼疮性肾炎相关的传统因素,如年龄和抗双链DNA,以及HLA - DRB1*1503,此前尚未发现其与狼疮性肾炎、新发或蛋白尿恶化有关。