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Genetics and gene manipulation therapy of premature coronary artery disease.

机译:早发冠心病的遗传学和基因操纵疗法。

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摘要

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.
机译:尽管最近有科学上的显着进步,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,并且对高危患者的识别尚需基于客观的科学测试。消除CAD家族史目前仍是唯一可用于识别具有遗传易感性患者的筛查工具。归因于基因的CAD风险似乎在年轻时最为显着,这可能解释了该疾病缺乏明确的标志物的原因。因此,针对年轻的CAD患者的候选基因关联研究将更有可能确定真正的遗传风险。在本报告中,我们回顾了过早CAD的已知遗传风险因素。我们还将讨论冠状动脉搭桥手术后CAD以及静脉移植物动脉粥样硬化的潜在基因操纵疗法。

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