Hospital for Special Surgery, New York, New York.
University of California School of Medicine, San Francisco.
Arthritis Care Res (Hoboken). 2018 Feb;70(2):230-235. doi: 10.1002/acr.23263. Epub 2017 Dec 29.
We examined rates of adverse pregnancy outcomes (APO) by race/ethnicity among women with systemic lupus erythematosus (SLE), with and without antiphospholipid antibodies (aPL), and whether socioeconomic status (SES) accounted for differences.
Data were from the PROMISSE (Predictors of Pregnancy Outcome: Biomarkers in Antiphospholipid Antibody Syndrome and Systemic Lupus Erythematosus) study, a multicenter study that enrolled 346 patients with SLE and 62 patients with SLE and aPL (50% white, 20% African American, 17% Hispanic, 12% Asian/Pacific Islander). Measures of SES were educational attainment, median community income, and community education. Logistic regression analyses were conducted to determine odds of APO for each racial/ethnic group, controlling first for age and clinical variables, and then for SES.
The frequency of APO in white women with SLE, with and without aPL, was 29% and 11%, respectively. For African American and Hispanic women it was approximately 2-fold greater. In African American women with SLE alone, adjustment for clinical variables attenuated the odds ratio (OR) from 2.7 (95% confidence interval [95% CI] 1.3-5.5) to 2.3 (95% CI 1.1-5.1), and after additional adjustment for SES, there were no longer significant differences in APO compared to whites. In contrast, in SLE patients with aPL, whites, African Americans, and Hispanics had markedly higher risks of APO compared to white SLE patients without aPL (OR 3.5 [95% CI 1.4-7.7], OR 12.4 [95% CI 1.9-79.8], and OR 10.4 [95% CI 2.5-42.4], respectively), which were not accounted for by clinical or SES covariates.
This finding suggests that for African American women with SLE without aPL, SES factors are key contributors to disparities in APO, despite monthly care from experts, whereas other factors contribute to disparities in SLE with aPL.
我们研究了红斑狼疮(SLE)患者和抗磷脂抗体(aPL)阳性或阴性的 SLE 患者的不良妊娠结局(APO)发生率,并探讨了社会经济地位(SES)是否导致了差异。
数据来自 PROMISSE(预测妊娠结局:抗磷脂抗体综合征和系统性红斑狼疮中的生物标志物)研究,这是一项多中心研究,共纳入了 346 名 SLE 患者和 62 名 SLE 和 aPL 患者(50%为白人,20%为非裔美国人,17%为西班牙裔,12%为亚洲/太平洋岛民)。SES 测量指标包括教育程度、社区中位数收入和社区教育水平。我们采用逻辑回归分析来确定每个种族/族裔群体的 APO 比值比(OR),首先控制年龄和临床变量,然后控制 SES。
白人 SLE 患者伴有和不伴有 aPL 的 APO 发生率分别为 29%和 11%。非裔美国人和西班牙裔的发生率则约为两倍。在仅有 SLE 的非裔美国女性中,调整临床变量后,OR 从 2.7(95%置信区间 [95%CI] 1.3-5.5)降至 2.3(95%CI 1.1-5.1),并且在进一步调整 SES 后,与白人相比,APO 差异不再显著。相比之下,在有 aPL 的 SLE 患者中,与无 aPL 的白人 SLE 患者相比,白人、非裔美国人和西班牙裔的 APO 风险明显更高(OR 3.5 [95%CI 1.4-7.7],OR 12.4 [95%CI 1.9-79.8],OR 10.4 [95%CI 2.5-42.4]),这与临床或 SES 协变量无关。
这项研究表明,对于无 aPL 的 SLE 非裔美国女性,尽管每月都有专家进行护理,但 SES 因素是导致 APO 差异的关键因素,而其他因素则导致了有 aPL 的 SLE 患者的差异。