McCarthy Jeanette J
School of Public Health, San Diego State University, 5500 Campanile Drive, San Diego, CA 92182-4162, USA.
Nutr Metab Cardiovasc Dis. 2007 Feb;17(2):153-61. doi: 10.1016/j.numecd.2006.01.005. Epub 2006 Mar 31.
Despite decades of research, the genetic basis of coronary heart disease and its metabolic risk factors is poorly understood. Few studies consider that sex may modify the effect of gene variants on disease. Investigation of gene by sex interaction may help to elucidate underlying genetic susceptibilities and explain the sexual dimorphism of these complex traits.
The aim of this review is to summarize evidence for gene by sex interaction in the etiology of coronary heart disease and the metabolic syndrome.
Published literature was examined in the areas of familial aggregation of coronary heart disease; heritability of body mass, insulin resistance, hypertension and dyslipidemia; genome-wide linkage analysis in humans and rodents; and large-scale genetic association studies. Possible mechanisms of gene by sex interaction are discussed including X-linked inheritance, confounding by risk factors and the effect of sex hormones.
The strongest evidence for gene by sex interaction in relation to coronary heart disease and the metabolic syndrome is in the etiology of body mass, insulin resistance and possibly dyslipidemia. Genetic studies of these traits would benefit from taking sex differences into account. Alternative mechanisms underlying gene by sex interaction, besides obvious sex hormone differences, should be considered.
尽管经过数十年研究,但冠心病及其代谢危险因素的遗传基础仍知之甚少。很少有研究考虑性别可能会改变基因变异对疾病的影响。对基因与性别的相互作用进行研究可能有助于阐明潜在的遗传易感性,并解释这些复杂性状的性别差异。
本综述的目的是总结冠心病和代谢综合征病因中基因与性别相互作用的证据。
对已发表文献在冠心病家族聚集、体重、胰岛素抵抗、高血压和血脂异常的遗传性、人类和啮齿动物的全基因组连锁分析以及大规模遗传关联研究等领域进行了审查。讨论了基因与性别相互作用的可能机制,包括X连锁遗传、危险因素的混杂作用以及性激素的影响。
关于冠心病和代谢综合征,基因与性别相互作用的最有力证据存在于体重、胰岛素抵抗以及可能的血脂异常的病因中。这些性状的遗传研究若考虑性别差异将受益匪浅。除了明显的性激素差异外,还应考虑基因与性别相互作用的其他潜在机制。