Service of Cardiology, Centre de Recherche CHU Sainte Justine, Université de Montréal, Montréal, Québec, Canada.
Can J Cardiol. 2013 Jul;29(7):803-10. doi: 10.1016/j.cjca.2013.03.011. Epub 2013 May 22.
Heart failure is a major problem in the patient with congenital heart disease. Normally interpreted as a sequela of surgical interventions or abnormal preoperative loading conditions, there is increasing evidence that congenital heart malformations and abnormal ventricular function can have the same underlying genetic cause. With the changing demographic characteristics and increasing complexity of care for patients with congenital heart disease, it can be anticipated that heart failure will be a rapidly growing concern in our field. In this article, we aim to give an overview of recent findings from mouse and human models that highlight shared pathways for the regulation of cardiac development and contractility, and their importance for medical care in the near future.
心力衰竭是先天性心脏病患者的一个主要问题。通常被解释为手术干预或异常术前负荷条件的后遗症,但越来越多的证据表明,先天性心脏畸形和异常心室功能可能有相同的潜在遗传原因。随着先天性心脏病患者人口统计学特征的变化和护理复杂性的增加,可以预计心力衰竭将成为我们领域中一个迅速增长的关注点。在本文中,我们旨在概述来自小鼠和人类模型的最新发现,这些发现强调了心脏发育和收缩性调节的共同途径,以及它们对未来医疗保健的重要性。