Tohoku University Graduate School of Medicine, Sendai, Japan.
Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.
Acta Obstet Gynecol Scand. 2024 Jun;103(6):1192-1200. doi: 10.1111/aogs.14820. Epub 2024 Mar 7.
Developmental delay at an early age indicates the probability of continued problems after school age. Hypertensive disorders of pregnancy (HDP) are associated with developmental delays in offspring, with inconsistent outcomes. Neonatal outcomes vary according to HDP exposure and are relevant to development in later years. Here we aimed to clarify the relationship between HDP and developmental delay in offspring and whether neonatal outcomes mediate this association.
We used data from 5934 mother-child pairs from the Tohoku Medical Megabank Project Birth and Three-Generation Cohort Study, a prospective cohort study conducted in Japan between July 2013 and March 2017. The Ages and Stages Questionnaires, third edition, at 24 and 42 months of age, measured developmental delay in five areas. We performed multivariate quasi-Poisson regression and causal mediation analysis by neonatal outcomes.
At 24 months of age, compared to offspring born from normotensive mothers, offspring born from HDP-affected mothers were more likely to experience developmental delay (risk ratio [RR] 1.29, 95% confidence interval [CI]: 1.09-1.52) in the areas of communication (RR 1.21, 95% CI: 1.00-1.45) and personal-social (RR 1.15, 95% CI: 1.03-1.28). This association was mediated by neonatal outcomes: preterm birth, neonatal asphyxia, NICU admission, and neonatal small head circumference. No association was observed between HDP and developmental delay at 42 months of age.
Exposure to HDP during fetal life is associated with offspring developmental delay. This association is partly mediated by neonatal outcomes.
儿童早期发育迟缓表明其在学龄后持续存在问题的可能性。妊娠高血压疾病(HDP)与后代发育迟缓有关,但结果不一致。新生儿结局因 HDP 暴露而异,与日后的发展相关。在此,我们旨在阐明 HDP 与后代发育迟缓之间的关系,以及新生儿结局是否在其中起中介作用。
我们使用了日本 2013 年 7 月至 2017 年 3 月期间进行的 Tohoku 医学 Megabank 项目母婴三代队列前瞻性研究中的 5934 对母婴数据。在 24 个月和 42 个月时,使用《年龄与阶段问卷》(第三版)测量五个领域的发育迟缓。我们通过新生儿结局进行了多变量拟泊松回归和因果中介分析。
在 24 个月时,与正常血压母亲所生的后代相比,HDP 母亲所生的后代在沟通(RR 1.21,95%置信区间[CI]:1.00-1.45)和个人社会(RR 1.15,95%CI:1.03-1.28)领域更有可能出现发育迟缓。这种关联部分由新生儿结局介导:早产、新生儿窒息、NICU 入院和新生儿小头围。在 42 个月时,未观察到 HDP 与发育迟缓之间存在关联。
胎儿期暴露于 HDP 与后代发育迟缓有关。这种关联部分由新生儿结局介导。