Race, Ethnicity, and Disparities in the Risk of End-Organ Lupus Manifestations Following a Systemic Lupus Erythematosus Diagnosis in a Multiethnic Cohort

被引:14
作者
Aguirre, Alfredo [1 ]
Izadi, Zara [1 ]
Trupin, Laura [1 ]
Barbour, Kamil E. [2 ]
Greenlund, Kurt J. [2 ]
Katz, Patti [1 ]
Lanata, Cristina [3 ]
Criswell, Lindsey [3 ]
Dall'Era, Maria [1 ]
Yazdany, Jinoos [1 ]
机构
[1] Univ Calif San Francisco, San Francisco, CA 94143 USA
[2] Ctr Dis Control & Prevent, Atlanta, GA USA
[3] Natl Human Genome Res Inst, Natl Inst Hlth, Bethesda, MD USA
基金
美国医疗保健研究与质量局;
关键词
DISEASE-ACTIVITY; REVISED CRITERIA; NEPHRITIS; MORTALITY; LUMINA; DAMAGE; CLASSIFICATION; ASSOCIATION; PREVALENCE; CALIFORNIA;
D O I
10.1002/acr.24892
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Data on the onset of lupus manifestations across multiple organ domains and in diverse populations are limited. The objective was to analyze racial and ethnic differences in the risk of end-organ lupus manifestations following systemic lupus erythematosus (SLE) diagnosis in a multiethnic cohort. Methods The California Lupus Epidemiology Study (CLUES) is a longitudinal study of SLE. Data on major end-organ lupus manifestations were collected and categorized by organ system: renal, hematologic, neurologic, cardiovascular, and pulmonary. Multiorgan disease was defined as manifestations in >= 2 of these distinct organ systems. Kaplan-Meier curves assessed end-organ disease-free survival, and Cox proportional hazards regression estimated the rate of end-organ disease following SLE diagnosis, adjusting for age at diagnosis, sex, and self-reported race and ethnicity (White, Hispanic, Black, and Asian). Results Of 326 participants, 89% were female; the mean age was 45 years. Self-reported race and ethnicity were 30% White, 23% Hispanic, 11% Black, and 36% Asian. Multiorgan disease occurred in 29%. Compared to White participants, Hispanic and Asian participants had higher rates, respectively, of renal (hazard ratio [HR] 2.9 [95% confidence interval (95% CI) 1.8-4.7], HR 2.9 [95% CI 1.9-4.6]); hematologic (HR 2.7 [95% CI 1.3-5.7], HR 2.1 [95% CI 1.0-4.2]); and multiorgan disease (HR 3.3 [95% CI 1.8-5.9], HR 2.5 [95% CI 1.4-4.4]) following SLE diagnosis. Conclusion We found heightened risks of developing renal, hematologic, and multiorgan disease following SLE diagnosis among Hispanic and Asian patients with SLE, as well as a high burden of multiorgan disease among CLUES participants.
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收藏
页码:34 / 43
页数:10
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