Department of Medicine Solna, Clinical Epidemiology Division, Karolinska Institutet, Karolinska University Hospital, D1: 04, Stockholm SE-171 76, Sweden.
School of Population and Public Health, University of British Columbia, 2206 East Mall, Vancouver BC V6T 1Z3, Canada.
Eur Heart J. 2024 Oct 7;45(38):4111-4123. doi: 10.1093/eurheartj/ehae547.
A variety of maternal heart conditions are associated with abnormal placentation and reduced foetal growth. However, their impact on offspring's long-term cardiovascular health is poorly studied. This study aims to investigate the association between intrauterine exposure to pre-existing maternal cardiovascular disease (CVD) and offspring CVD occurring from infancy to early adulthood, using paternal CVD as a negative control.
This nationwide cohort study used register data of live singletons without major malformations or congenital heart disease born between 1992 and 2019 in Sweden. Hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated using Cox proportional hazards models, adjusted for essential maternal characteristics. Paternal CVD served as a negative control for assessment of unmeasured genetic and environmental confounding.
Of the 2 597 786 offspring analysed (49.1% female), 26 471 (1.0%) were born to mothers with pre-existing CVD. During a median follow-up of 14 years (range 1-29 years), 17 382 offspring were diagnosed with CVD. Offspring of mothers with CVD had 2.09 times higher adjusted HR of CVD (95% CI 1.83, 2.39) compared with offspring of mothers without CVD. Compared with maternal CVD, paternal CVD showed an association of smaller magnitude (HR 1.49, 95% CI 1.32, 1.68). Increased hazards of offspring CVD were also found when stratifying maternal CVD into maternal arrhythmia (HR 2.94, 95% CI 2.41, 3.58), vascular (HR 1.59, 95% CI 1.21, 2.10), and structural heart diseases (HR 1.48, 95% CI 1.08, 2.02).
Maternal CVD was associated with an increased risk of CVD in offspring during childhood and young adulthood. Paternal comparison suggests that genetic or shared familial factors may not fully explain this association.
多种母体心脏疾病与异常胎盘形成和胎儿生长受限有关。然而,它们对后代长期心血管健康的影响研究甚少。本研究旨在调查宫内暴露于母亲先前存在的心血管疾病(CVD)与婴儿至成年早期发生的后代 CVD 之间的关联,以父亲 CVD 为阴性对照。
这是一项全国性队列研究,使用瑞典 1992 年至 2019 年间出生的无重大畸形或先天性心脏病的活单胎儿的登记数据。使用 Cox 比例风险模型估计危险比(HRs)和 95%置信区间(CIs),并根据基本的母体特征进行调整。父亲 CVD 作为评估未测量的遗传和环境混杂因素的阴性对照。
在分析的 2597786 名后代中(49.1%为女性),有 26471 名(1.0%)出生于患有先前存在的 CVD 的母亲。在中位随访 14 年(范围 1-29 年)期间,有 17382 名后代被诊断为 CVD。与无 CVD 的母亲相比,CVD 母亲的后代发生 CVD 的调整后 HR 高出 2.09 倍(95%CI 1.83,2.39)。与母亲 CVD 相比,父亲 CVD 的关联幅度较小(HR 1.49,95%CI 1.32,1.68)。当将母亲 CVD 分层为心律失常(HR 2.94,95%CI 2.41,3.58)、血管(HR 1.59,95%CI 1.21,2.10)和结构性心脏病(HR 1.48,95%CI 1.08,2.02)时,后代 CVD 的发生风险也有所增加。
母亲 CVD 与儿童和青年期后代 CVD 风险增加相关。与父亲的比较表明,遗传或共同的家族因素可能无法完全解释这种关联。