Department of Obstetrics and Gynecology, University of Utah Health, Salt Lake City, Utah, USA.
Department of Obstetrics and Gynecology, Ohio State University, Columbus, Ohio, USA.
BJOG. 2023 Sep;130(10):1197-1206. doi: 10.1111/1471-0528.17486. Epub 2023 Apr 17.
To assess the relationship between allostatic load, a measure of cumulative chronic stress in early pregnancy and cardiovascular disease risk, 2-7 years postpartum, and pathways contributing to racial disparities in cardiovascular disease risk.
Secondary analysis of a prospective cohort study.
Pregnant women.
Our primary exposure was high allostatic load in the first trimester, defined as at least 4 of 12 biomarkers (systolic blood pressure, diastolic blood pressure, body mass index, cholesterol, low-density lipoprotein, high-density lipoprotein, high-sensitivity C-reactive protein, triglycerides, insulin, glucose, creatinine and albumin) in the unfavourable quartile. Logistic regression was used to test the association between high allostatic load and main outcome adjusted for confounders: time from index pregnancy and follow up, age, education, smoking, gravidity, bleeding in the first trimester, index adverse pregnancy outcomes, and health insurance. Each main outcome component and allostatic load were analysed secondarily. Mediation and moderation analyses assessed the role of high allostatic load in racial disparities of cardiovascular disease risk.
Incident cardiovascular disease risk: hypertension, or metabolic disorders.
Cardiovascular disease risk was identified in 1462/4022 individuals (hypertension: 36.6%, metabolic disorder: 15.4%). After adjustment, allostatic load was associated with cardiovascular disease risk (adjusted odds ratio [aOR] 2.0, 95% CI 1.8-2.3), hypertension (aOR 2.1, 95% CI 1.8-2.4) and metabolic disorder (aOR 1.7, 95% CI 1.5-2.1). Allostatic load was a partial mediator between race and cardiovascular disease risk. Race did not significantly moderate this relationship.
High allostatic load during pregnancy is associated with cardiovascular disease risk. The relationships between stress, subsequent cardiovascular risk and race warrant further study.
评估妊娠早期累积性慢性应激的生物压力指标与心血管疾病风险之间的关系,以及导致心血管疾病风险种族差异的途径。
前瞻性队列研究的二次分析。
多中心人群,孕妇。
我们的主要暴露是妊娠早期高生物压力,定义为至少有 12 种生物标志物(收缩压、舒张压、体重指数、胆固醇、低密度脂蛋白、高密度脂蛋白、高敏 C 反应蛋白、甘油三酯、胰岛素、血糖、肌酐和白蛋白)中的 4 种处于不利四分位数。使用逻辑回归检验高生物压力与主要结局之间的关联,该结局在调整混杂因素后进行测试:从指数妊娠和随访开始的时间、年龄、教育、吸烟、孕次、妊娠早期出血、指数不良妊娠结局和健康保险。次要分析每个主要结局成分和生物压力。中介和调节分析评估了高生物压力在心血管疾病风险种族差异中的作用。
心血管疾病风险:高血压或代谢紊乱。
在 4022 名个体中,有 1462 人(高血压:36.6%,代谢紊乱:15.4%)确定了心血管疾病风险。调整后,生物压力与心血管疾病风险(调整后的优势比[aOR]2.0,95%可信区间[CI]1.8-2.3)、高血压(aOR 2.1,95%CI 1.8-2.4)和代谢紊乱(aOR 1.7,95%CI 1.5-2.1)相关。生物压力是种族与心血管疾病风险之间的部分中介。种族并没有显著调节这种关系。
妊娠期间高生物压力与心血管疾病风险相关。压力、随后的心血管风险与种族之间的关系值得进一步研究。