| Literature DB >> 24275306 |
Akl C Fahed1, Amy E Roberts, Seema Mital, Neal K Lakdawala.
Abstract
Heart failure (HF) is a common cause of morbidity and mortality in congenital heart disease (CHD), with increasing prevalence because of improved treatment options and outcomes. Genetic factors and acquired postnatal factors in CHD might play a major role in the progression to HF. This article proposes 3 routes that lead to HF in CHD: rare monogenic entities that cause both CHD and HF; severe CHD lesions in which acquired hemodynamic effects of CHD or surgery result in HF; and, most commonly, a combined effect of complex genetics in overlapping pathways and acquired stressors caused by the primary lesion. Published by Elsevier Inc.Entities:
Keywords: Adult; Congenital heart disease; Genomics; Heart failure
Mesh:
Year: 2014 PMID: 24275306 PMCID: PMC3874878 DOI: 10.1016/j.hfc.2013.09.017
Source DB: PubMed Journal: Heart Fail Clin ISSN: 1551-7136 Impact factor: 3.179