Piacentini Gerardo, Digilio M Cristina, Sarkozy Anna, Placidi Silvia, Dallapiccola Bruno, Marino Bruno
Pediatric Cardiology, Department of Pediatrics, La Sapienza University, Rome, Italy.
J Cardiovasc Med (Hagerstown). 2007 Jan;8(1):7-11. doi: 10.2459/01.JCM.0000247428.51828.51.
Congenital heart defects (CHDs) are the most common birth defects in humans and over the last 20 years significant progress has been made in the understanding of the molecular and genetic determinants of an increasing number of CHDs. Fundamental to this progress has been the contribution of five fields of research: the epidemiological results of the Baltimore-Washington Infant Study (BWIS); the pathogenetic classification introduced by Clark; the Human Genome Project; genotype-phenotype correlation and familial recurrence studies; and transgenic animals. The recently advanced cytogenetic techniques can now detect subtle rearrangements in chromosomes, which may be overlooked by standard methods and, more recently, molecular instruments such as linkage analysis and positional cloning are being used to identify genes causing Mendelian monogenic syndromes with CHDs, such as Holt-Oram, Ellis-van Creveld and Noonan/LEOPARD syndromes. Finally, useful information is yet available with regard to genes causing isolated CHDs in individuals who do not have a genetic syndrome (an example is the mutation of NKX2.5 and GATA4 genes causing atrial septal defect). The future perspectives for the genetics of CHDs will involve three fields of interest: diagnosis; therapy; and prognosis.
先天性心脏病(CHD)是人类最常见的出生缺陷,在过去20年里,在了解越来越多CHD的分子和遗传决定因素方面取得了重大进展。这一进展的基础是五个研究领域的贡献:巴尔的摩-华盛顿婴儿研究(BWIS)的流行病学结果;克拉克提出的病因分类;人类基因组计划;基因型-表型相关性和家族复发研究;以及转基因动物。最近发展起来的细胞遗传学技术现在可以检测染色体中的细微重排,而这些重排可能会被标准方法忽略,并且最近,诸如连锁分析和定位克隆等分子手段正被用于识别导致伴有CHD的孟德尔单基因综合征的基因,如 Holt-Oram、Ellis-van Creveld 和 Noonan/LEOPARD 综合征。最后,对于没有遗传综合征的个体中导致孤立性CHD的基因也有了有用的信息(例如导致房间隔缺损的NKX2.5和GATA4基因突变)。CHD遗传学的未来前景将涉及三个感兴趣的领域:诊断;治疗;以及预后。