Lusis Aldons J
Department of Medicine, University of California, Los Angeles, CA 90095-1679, USA.
Trends Cardiovasc Med. 2003 Nov;13(8):309-16. doi: 10.1016/j.tcm.2003.08.001.
The common forms of cardiovascular disease (CVD) have a complex etiology, involving multiple genetic influences and important environmental interactions. Because of this complexity, it has proved difficult to apply the positional cloning approaches that have revolutionized understanding of Mendelian (single-gene) disorders; and the understanding of the genetics of CVD and its underlying cause, atherosclerosis, remains poor. This review, organized into 10 broad questions, summarizes the understanding of the genetics of common, complex forms of CVD. Implications for DNA-based diagnosis, pharmacogenetics, and risk assessment are also discussed.
心血管疾病(CVD)的常见形式病因复杂,涉及多种基因影响以及重要的环境相互作用。由于这种复杂性,已证明难以应用那些彻底改变了对孟德尔(单基因)疾病理解的定位克隆方法;并且对心血管疾病及其潜在病因动脉粥样硬化的遗传学理解仍然不足。本综述分为10个宽泛的问题,总结了对常见复杂形式心血管疾病遗传学的理解。还讨论了对基于DNA的诊断、药物遗传学和风险评估的影响。