Rashmi Dhital, Rebecca J Baer, Dilli R Poudel, Tracy M Frech, Christina Chambers
{"title":"Racial differences in cardiovascular events and adverse pregnancy outcomes among pregnant individuals with SLE.","authors":"Rashmi Dhital, Rebecca J Baer, Dilli R Poudel, Tracy M Frech, Christina Chambers","doi":"10.1136/lupus-2025-001846","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>We aimed to characterise differences in the occurrence of maternal cardiovascular events (CVEs) and adverse pregnancy outcomes (APOs) in each of four racial/ethnic groups compared with non-Hispanic white women with SLE and to evaluate whether the relationship between CVEs and APOs differed across or within racial/ethnic groups.</p><p><strong>Methods: </strong>Using a California population-based birth cohort (2005-2020), we identified pregnant individuals with SLE via International Classification of Diseases codes from maternal discharge records. Self-reported racial/ethnic groups were categorised as Asian, Hispanic, non-Hispanic black, non-Hispanic white and other. Individuals with reported race or ethnicity as 'unknown' or 'not stated' were excluded from the study. Log-linear regression estimated adjusted relative risks (aRRs) of CVEs and APOs in each racial/ethnic group compared with non-Hispanic white individuals, adjusting for a propensity score derived from maternal age, payer, education, comorbidities and SLE-related variables. We performed CVE-stratified analyses for racial/ethnic differences in APOs and examined associations between CVEs and APOs within each racial/ethnic group.</p><p><strong>Results: </strong>Among 8188 liveborn singletons from women with SLE, non-Hispanic black women had the highest prevalence of maternal CVEs (4.0% vs 1.6-2.0% in other groups), maternal APOs (24.6% vs 13.5-17.2%) and infant APOs (54.6% vs 34.6-49.4%). Relative to non-Hispanic white women, non-Hispanic black women had an aRR of 1.6 (95% CI 0.9 to 2.6) for maternal CVEs and 1.3 (95% CI 1.1 to 1.6) for maternal APOs, whereas infant APO risks were significantly higher across three of four racial/ethnic groups compared with non-Hispanic white women.</p><p><strong>Conclusions: </strong>Non-Hispanic black women exhibited the highest absolute burden for the adverse outcomes studied. Relative to non-Hispanic white individuals, elevated adjusted risks based on race/ethnicity were most consistent for infant APOs, whereas elevated risks for maternal APOs and CVEs were found primarily among non-Hispanic black individuals. Social drivers of health need consideration while caring for pregnant individuals with SLE.</p>","PeriodicalId":18126,"journal":{"name":"Lupus Science & Medicine","volume":"13 2","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2026-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13583854/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lupus Science & Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1136/lupus-2025-001846","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: We aimed to characterise differences in the occurrence of maternal cardiovascular events (CVEs) and adverse pregnancy outcomes (APOs) in each of four racial/ethnic groups compared with non-Hispanic white women with SLE and to evaluate whether the relationship between CVEs and APOs differed across or within racial/ethnic groups.
Methods: Using a California population-based birth cohort (2005-2020), we identified pregnant individuals with SLE via International Classification of Diseases codes from maternal discharge records. Self-reported racial/ethnic groups were categorised as Asian, Hispanic, non-Hispanic black, non-Hispanic white and other. Individuals with reported race or ethnicity as 'unknown' or 'not stated' were excluded from the study. Log-linear regression estimated adjusted relative risks (aRRs) of CVEs and APOs in each racial/ethnic group compared with non-Hispanic white individuals, adjusting for a propensity score derived from maternal age, payer, education, comorbidities and SLE-related variables. We performed CVE-stratified analyses for racial/ethnic differences in APOs and examined associations between CVEs and APOs within each racial/ethnic group.
Results: Among 8188 liveborn singletons from women with SLE, non-Hispanic black women had the highest prevalence of maternal CVEs (4.0% vs 1.6-2.0% in other groups), maternal APOs (24.6% vs 13.5-17.2%) and infant APOs (54.6% vs 34.6-49.4%). Relative to non-Hispanic white women, non-Hispanic black women had an aRR of 1.6 (95% CI 0.9 to 2.6) for maternal CVEs and 1.3 (95% CI 1.1 to 1.6) for maternal APOs, whereas infant APO risks were significantly higher across three of four racial/ethnic groups compared with non-Hispanic white women.
Conclusions: Non-Hispanic black women exhibited the highest absolute burden for the adverse outcomes studied. Relative to non-Hispanic white individuals, elevated adjusted risks based on race/ethnicity were most consistent for infant APOs, whereas elevated risks for maternal APOs and CVEs were found primarily among non-Hispanic black individuals. Social drivers of health need consideration while caring for pregnant individuals with SLE.
期刊介绍:
Lupus Science & Medicine is a global, peer reviewed, open access online journal that provides a central point for publication of basic, clinical, translational, and epidemiological studies of all aspects of lupus and related diseases. It is the first lupus-specific open access journal in the world and was developed in response to the need for a barrier-free forum for publication of groundbreaking studies in lupus. The journal publishes research on lupus from fields including, but not limited to: rheumatology, dermatology, nephrology, immunology, pediatrics, cardiology, hepatology, pulmonology, obstetrics and gynecology, and psychiatry.