Gkrouzman Elena, Peng Mary, Davis-Porada Julia, Kirou Kyriakos A
Hospital for Special Surgery, New York, New York.
Columbia University Vagelos College of Physicians and Surgeons, New York, New York.
Arthritis Care Res (Hoboken). 2022 Apr;74(4):656-664. doi: 10.1002/acr.24508. Epub 2022 Mar 3.
The risk of thrombotic events is elevated in patients with systemic lupus erythematosus (SLE) compared to the general population and has been attributed to both systemic inflammation and to the presence of antiphospholipid antibodies (aPLs). Our objective was to examine differences in aPL prevalence in White and African American patients with SLE and venous thromboembolic (VTE) events, and to compare inflammatory markers at the time of a VTE event.
Records of White and African American patients with SLE and VTE events were retrieved from a rheumatology practice based at an academic hospital. A clinically significant aPL profile was defined as anti-cardiolipin IgG/IgM and/or anti-β -glycoprotein I IgG/IgM ≥40 units, and/or positive lupus anticoagulant ≥1.3. Logistic regression was used to determine predictors of a clinically significant aPL profile.
Ninety-seven patients fulfilled American College of Rheumatology and/or 2012 Systemic Lupus Erythematosus International Collaborating Clinics classification criteria for SLE, had a history of VTE events, and had available aPL tests (59 White and 38 African American patients). African American patients were 66% less likely (95% confidence interval 0.12-0.96; P = 0.04) to have a clinically significant aPL profile compared to White patients in multivariable regression. Triple positivity was most frequent among White patients, while 7 of 8 African American patients had a positive lupus anticoagulant test. At the time of a VTE event, African American patients had significantly higher levels of anti-double-stranded DNA (P = 0.02), lower hemoglobin (P = 0.01), and higher erythrocyte sedimentation rate (P = 0.008).
Among patients with SLE and VTE events, African American patients were less likely to have a clinically significant aPL profile compared to White patients, indicating that a negative aPL profile in African American patients does not decrease VTE risk.
与普通人群相比,系统性红斑狼疮(SLE)患者发生血栓事件的风险升高,这归因于全身炎症和抗磷脂抗体(aPLs)的存在。我们的目的是研究白种人和非裔美国SLE患者及静脉血栓栓塞(VTE)事件中aPL患病率的差异,并比较VTE事件发生时的炎症标志物。
从一家学术医院的风湿病科获取白种人和非裔美国SLE及VTE事件患者的记录。具有临床意义的aPL谱定义为抗心磷脂IgG/IgM和/或抗β2糖蛋白I IgG/IgM≥40单位,和/或狼疮抗凝物阳性≥1.3。采用逻辑回归确定具有临床意义的aPL谱的预测因素。
97例患者符合美国风湿病学会和/或2012年系统性红斑狼疮国际协作临床分类标准的SLE,有VTE事件病史,且有可用的aPL检测结果(59例白种人和38例非裔美国患者)。在多变量回归中,与白种人患者相比,非裔美国患者具有临床意义的aPL谱的可能性低66%(95%置信区间0.12 - 0.96;P = 0.04)。三联阳性在白种人患者中最常见,而8例非裔美国患者中有7例狼疮抗凝物检测呈阳性。在VTE事件发生时,非裔美国患者的抗双链DNA水平显著更高(P = 0.02),血红蛋白更低(P = 0.01),红细胞沉降率更高(P = 0.008)。
在SLE和VTE事件患者中,与白种人患者相比,非裔美国患者具有临床意义的aPL谱的可能性较小,这表明非裔美国患者aPL谱阴性并不会降低VTE风险。