利用基因组数据评估多因素冠状动脉疾病。

Elisabeth Widén, Samuli Ripatti
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引用次数: 0

摘要

过去几年的科学进步使基于全基因组信息的疾病个性化预防和治疗成为可能。例如,已经确定了几十个影响冠状动脉疾病风险的基因组区域。芬兰和国际纵向研究都表明,如果既基于新发现的遗传风险因素,又基于长期公认的传统风险因素(如年龄、性别、吸烟、血压和血脂水平),冠状动脉疾病的风险评估可以显著改善。在这篇综述中,我们以冠状动脉疾病为例,介绍了最近的研究,旨在加强基因组信息与传统危险因素的结合,以评估具有公共卫生重要性的常见疾病的风险。我们介绍由我们开发的KardioKompassi工具,该工具综合利用个人的遗传特征结合常规健康信息来评估冠状动脉疾病的风险。我们还讨论了新开发的下一代风险预测工具为促进健康提供的前景和机遇。”
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of multifactorial coronary artery disease by utilizing genomic data.

The scientific advances in the past few years have enabled individualized prevention and treatment of diseases on the basis of genome-wide information. For example, dozens of genomic regions affecting the risk for coronary artery disease have been identified. Both Finnish and international longitudinal studies show that the risk assessment of coronary artery disease can be significantly improved if the estimate is based both on the newly discovered hereditary risk factors and the long-recognized traditional risk factors, e.g. age, gender, smoking, blood pressure, and serum lipid levels. In this review, by using coronary artery disease as an example, we present recent research aiming at enhancing the use of genome information in combination with traditional risk factors for the assessment of the risk for common disease of public health importance. We introduce the KardioKompassi tool, developed by us, which comprehensively utilizes the genetic profile of an individual in combination with conventional health information to assess the risk for coronary artery disease. We also discuss the prospects and opportunities provided by the newly developed next-generation risk prediction tools to promote health."

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