Hypertension. 2023 May;80(5):e75-e89. doi: 10.1161/HYP.0000000000000227. Epub 2023 Mar 23.
There is increasing interest in the long-term cardiovascular health of women with complicated pregnancies and their affected offspring. Emerging antenatal risk factors such as preeclampsia appear to increase the risk of hypertension and cardiovascular disease across the life course in both the offspring and women after pregnancy. However, the antenatal programming mechanisms responsible are complex and incompletely understood, with roots in alterations in the development, structure, and function of the kidney, heart, vasculature, and brain. The renin-angiotensin-aldosterone system is a major regulator of maternal-fetal health through the placental interface, as well as kidney and cardiovascular tissue development and function. Renin-angiotensin-aldosterone system dysregulation plays a critical role in the development of pregnancy complications such as preeclampsia and programming of long-term adverse cardiovascular health in both the mother and the offspring. An improved understanding of antenatal renin-angiotensin-aldosterone system programming is crucial to identify at-risk individuals and to facilitate development of novel therapies to prevent and treat disease across the life course. Given the inherent complexities of the renin-angiotensin-aldosterone system, it is imperative that preclinical and translational research studies adhere to best practices to accurately and rigorously measure components of the renin-angiotensin-aldosterone system. This comprehensive synthesis of preclinical and translational scientific evidence of the mechanistic role of the renin-angiotensin-aldosterone system in antenatal programming of hypertension and cardiovascular disease will help (1) to ensure that future research uses best research practices, (2) to identify pressing needs, and (3) to guide future investigations to maximize potential outcomes. This will facilitate more rapid and efficient translation to clinical care and improve health outcomes.
人们越来越关注患有复杂妊娠的女性及其受影响后代的长期心血管健康。新出现的产前危险因素,如先兆子痫,似乎会增加后代和妊娠后女性整个生命周期内高血压和心血管疾病的风险。然而,负责的产前编程机制很复杂,且尚未完全被理解,其根源在于肾脏、心脏、血管和大脑的发育、结构和功能的改变。肾素-血管紧张素-醛固酮系统通过胎盘界面以及肾脏和心血管组织的发育和功能,是调节母婴健康的主要调节因子。肾素-血管紧张素-醛固酮系统失调在妊娠并发症(如先兆子痫)的发展以及母亲和后代长期不良心血管健康的编程中起着关键作用。对产前肾素-血管紧张素-醛固酮系统编程的更好理解对于确定高危人群以及促进开发预防和治疗整个生命周期疾病的新疗法至关重要。鉴于肾素-血管紧张素-醛固酮系统的固有复杂性,临床前和转化研究必须遵循最佳实践,以准确和严格地测量肾素-血管紧张素-醛固酮系统的各个组成部分。本综述综合了肾素-血管紧张素-醛固酮系统在产前高血压和心血管疾病编程中的机制作用的临床前和转化科学证据,将有助于:(1) 确保未来的研究使用最佳的研究实践;(2) 确定紧迫的需求;(3) 指导未来的研究以最大限度地发挥潜力。这将促进更快速和有效的临床护理转化,并改善健康结果。