Oxford Cardiovascular Clinical Research Facility, Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
Oxford Cardiovascular Clinical Research Facility, Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom,
Fetal Diagn Ther. 2020;47(5):373-386. doi: 10.1159/000501906. Epub 2019 Sep 18.
Formation of the human heart involves complex biological signals, interactions, specification of myocardial progenitor cells, and heart tube looping. To facilitate survival in the hypoxemic intrauterine environment, the fetus possesses structural, physiological, and functional cardiovascular adaptations that are fundamentally different from the neonate. At birth, upon separation from the placental circulation, the neonatal cardiovascular system takes over responsibility of vital processes for survival. The transition from the fetal to neonatal circulation is considered to be a period of intricate physiological, anatomical, and biochemical changes in the cardiovascular system. With a successful cardiopulmonary transition to the extrauterine environment, the fetal shunts are functionally modified or eliminated, enabling independent life. Investigations using medical imaging tools such as ultrasound and magnetic resonance imaging have helped to define normal and abnormal patterns of cardiac remodeling both in utero and ex utero. This has not only allowed for a better understanding of how congenital cardiac malformations alter the hemodynamic transition to the extrauterine environment but also how other more common complications during pregnancy including intrauterine growth restriction, preeclampsia, and preterm delivery adversely affect offspring cardiac remodeling during this early transitional period. This review article describes key cardiac progenitors involved in embryonic heart development; the cellular, physiological, and anatomical changes during the transition from fetal to neonatal circulation; as well as the unique impact that different pregnancy complications have on cardiac remodeling.
人类心脏的形成涉及复杂的生物信号、相互作用、心肌祖细胞的特化以及心管环曲。为了在低氧的宫内环境中生存,胎儿具有结构、生理和功能上的心血管适应,这些适应与新生儿有根本的不同。出生时,胎儿与胎盘循环分离后,新生儿心血管系统开始负责生存的重要过程。从胎儿循环到新生儿循环的转变被认为是心血管系统发生复杂的生理、解剖和生化变化的时期。随着心肺向体外环境的成功过渡,胎儿分流功能得到修正或消除,从而能够独立生存。使用超声和磁共振成像等医学成像工具的研究有助于确定宫内和宫外心脏重塑的正常和异常模式。这不仅使人们更好地了解先天性心脏畸形如何改变向体外环境的血液动力学过渡,还了解妊娠期间的其他更常见并发症,如宫内生长受限、子痫前期和早产,如何在这一早期过渡时期对后代心脏重塑产生不利影响。本文综述了胚胎心脏发育过程中涉及的关键心脏祖细胞;胎儿到新生儿循环过渡期间的细胞、生理和解剖变化;以及不同妊娠并发症对心脏重塑的独特影响。