University of Ottawa Heart Institute, Ottawa, Ontario, Canada.
Curr Opin Cardiol. 2012 May;27(3):221-7. doi: 10.1097/HCO.0b013e3283515b4b.
Prevention of coronary artery disease (CAD) is an appropriate goal for the 21st century. Randomized clinical studies consistently show a 30-40% reduction in mortality and morbidity by modifying known risk factors. However, genetic risk, estimated to account for 40-60% of susceptibility to CAD, has until recently been unknown. Comprehensive prevention will require knowledge of both.
The 21st century technology has responded to the challenge. Whereas the first genetic risk variant was not discovered until 2007 (9p21), a total of 36 genetic risk factors for CAD have been discovered and verified in large sample sizes. A startling discovery was that over two-thirds of these factors do not act through known risk factors or mechanisms. This obviously has great implications for the pathogenesis of CAD and presents many potential targets for new therapy. These genetic risk factors occur more commonly in the population than expected, with over half of them occurring in more than 50% of the population, and 10 of them occurring in at least 75% of the population.
The role of genetic risk factors in genetic screening for prevention of heart disease is yet to be defined. The technology is already available, but functional analysis may be a prerequisite for their clinical application.
预防冠状动脉疾病(CAD)是 21 世纪的适当目标。随机临床试验一致表明,通过改变已知的危险因素,可以将死亡率和发病率降低 30-40%。然而,直到最近,遗传风险(估计占 CAD 易感性的 40-60%)才被发现。全面预防需要两者兼知。
21 世纪的技术已经应对了这一挑战。尽管直到 2007 年才发现第一个遗传风险变异体(9p21),但已经在大量样本中发现并验证了总共 36 个 CAD 的遗传风险因素。一个惊人的发现是,这些因素中超过三分之二并非通过已知的危险因素或机制起作用。这显然对 CAD 的发病机制具有重大影响,并为新疗法提供了许多潜在的靶点。这些遗传风险因素在人群中的出现频率高于预期,其中超过一半的因素出现在超过 50%的人群中,有 10 个因素至少出现在 75%的人群中。
遗传风险因素在心脏病遗传筛查预防中的作用尚未确定。该技术已经可用,但功能分析可能是其临床应用的前提。