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Does SLE widen or narrow race/ethnic disparities in the risk of five co-morbid conditions? Evidence from a community-based outpatient care system

机译:SLE扩大或狭窄的种族/民族差异是否有五种共同病态条件的风险? 来自社区的门诊护理系统的证据

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Objective: The heterogeneous spectrum of systemic lupus erythematosus (SLE) often presents with secondary complications such as cardiovascular disease (CVD), infections and neoplasms. Our study assessed whether the presence of SLE independently increases or reduces the disparities, accounting for the already higher risk of these outcomes among racial/ethnic minority groups without SLE. Methods: We defined a cohort using electronic health records data (2005-2016) from a mixed-payer community-based outpatient setting in California serving patients of diverse racial/ethnic backgrounds. The eligible population included adult patients with SLE and matched non-SLE patients (>= 18 years old). SLE was the primary exposure. The following outcomes were identified: pneumonia, other infections, CVD and neoplasms. For each racial/ethnic group, we calculated the proportion of incident co-morbidities by SLE exposure, followed by logistic regression for each outcome with SLE as the exposure. We evaluated interaction on the additive and multiplicative scales by calculating the relative excess risk due to interaction and estimating the cross-product term in each model. Results: We identified 1036 SLE cases and 8875 controls. The incidence for all outcomes was higher among the SLE exposed. We found little difference in the odds of the outcomes associated with SLE across racial/ethnic groups, even after multivariable adjustment. This finding was consistent on the multiplicative and additive scales. Conclusion: We demonstrated that SLE status does not independently confer substantial interaction or heterogeneity by race/ethnicity toward the risk of pneumonia, other infections, CVD or neoplasms. Further studies in larger datasets are necessary to validate this novel finding.
机译:目的:全身性狼疮性红斑(SLE)的异质谱常用于次要并发症,如心血管疾病(CVD),感染和肿瘤。我们的研究评估了SLE是否存在独立增加或减少差距,占这些没有SLE的种族/少数群体之间这些结果的风险更高。方法:我们使用电子健康记录数据(2005-2016)从加利福尼亚州的混合付款人社区门诊环境中使用电子健康记录数据(2005-2016),服务于多元化的种族/民族背景。符合条件的人群包括SLE和匹配的非SLE患者的成人患者(> = 18岁)。 SLE是主要的曝光。确定了以下结果:肺炎,其他感染,CVD和肿瘤。对于每个种族/民族,我们通过SLE暴露计算了事故辅病原体的比例,随后对每个结果的逻辑回归为暴露。通过计算相互作用和估计每个模型中的横向产品术语,通过计算相对过量的风险来评估添加剂和乘法尺度的相互作用。结果:我们确定了1036个SLE案例和8875个控制。曝光的SLE中所有结果的发病率较高。我们发现与种族/族群的SLE相关的结果的几乎没有差异,即使在多变量调整后也是如此。这一发现在乘法和添加剂尺度上是一致的。结论:我们证明,SLE状态不会通过种族/种族对肺炎,其他感染,CVD或肿瘤的风险独立赋予大量相互作用或异质性。在较大数据集中进一步的研究是验证这部小型发现的必要条件。

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