Chaer Rabih A, Billeh Rana, Massad Malek G
Division of Cardiothoracic Surgery, Department of Surgery, The University of Illinois College of Medicine at Chicago, Chicago, IL 60612, USA.
Cardiology. 2004;101(1-3):122-30. doi: 10.1159/000075993.
Despite the notable recent scientific advances, our ability to detect and prevent premature coronary artery disease (CAD) remains limited, and the identification of patients at risk is yet to be based on objective scientific testing. Eliciting a family history of CAD currently remains the only available screening tool to identify patients with a genetic predisposition. The risk of CAD attributable to genes appears to be most significant at younger ages, and this may explain the lack of definite markers for the disease. Candidate gene association studies focusing on young patients with CAD will, therefore, be more likely to identify a true genetic risk. In this report, we review the known genetic risk factors for premature CAD. We also discuss the potential gene manipulation therapy of CAD as well as of vein graft atherosclerosis following coronary artery bypass surgery.
尽管近期取得了显著的科学进展,但我们检测和预防早发性冠状动脉疾病(CAD)的能力仍然有限,且识别高危患者尚未基于客观的科学检测。目前,询问CAD家族史仍是识别具有遗传易感性患者的唯一可用筛查工具。基因所致的CAD风险在年轻时似乎最为显著,这或许可以解释为何该疾病缺乏明确的标志物。因此,针对年轻CAD患者的候选基因关联研究更有可能识别出真正的遗传风险。在本报告中,我们回顾了已知的早发性CAD遗传风险因素。我们还讨论了CAD以及冠状动脉旁路移植术后静脉移植物动脉粥样硬化的潜在基因操纵治疗。