冠状动脉疾病的个性化管理

T. Kessler, H. Schunkert
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引用次数: 0

摘要

冠状动脉疾病和心肌梗死是发病率和死亡率的主要原因。在过去的几十年里,已经确定了几种可改变和不可改变的潜在疾病风险因素。最近,全基因组关联研究和下一代测序导致遗传风险因素的发现。这些遗传危险因素的知识已被证明有助于了解冠状动脉粥样硬化的病理生理学。他们的知识在风险预测和诊断方面也可能有用。最终,利用遗传信息和新型成像技术的综合方法将改善治疗策略,实现个性化医疗。在此,我们想总结这一研究领域的最新发现,并提供如何利用这些发展来改善冠状动脉粥样硬化及其后遗症的预防和治疗的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Personalized management of coronary artery disease
Coronary artery disease and myocardial infarction are main causes of morbidity and mortality. In the past decades, several modifiable and non-modifiable risk factors underlying the disease have been identified. Recently, genome-wide association studies and next generation sequencing led to the discovery of genetic risk factors. Knowledge of these genetic risk factors has been shown to help to understand the pathophysiology of coronary atherosclerosis. Their knowledge might also be useful in risk prediction and diagnostics. Ultimately, an integrated approach using genetic information and novel imaging technologies should improve treatment strategies towards a personalized medicine. Here, we want to summarize recent findings in this research field and provide insight how these developments could be used to improve prevention and treatment of coronary atherosclerosis and its sequelae.
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