遗传流行病学中的伦理问题

S. Fullerton, K. Edwards, M. Austin
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摘要

本章回顾了2003年人类DNA全序列的突破性发现,这一发现迅速开启了基因组学和大数据时代。它讨论了“精准医学”,这是指考虑基因、环境和生活方式的个体差异,从而设计出预防、检测、诊断和治疗健康状况的新方法的概念。它还将“精准公共卫生”描述为利用个体差异更精细地为高危人群量身定制预防干预措施并改善人口健康的相关努力。本章通过对人类种群中基因型、表型和环境数据的严格研究,解决了有关基因、环境、基因-基因和基因-环境相互作用在人类健康中的作用的科学问题。它处理基因组对健康和疾病的贡献,例如评估疾病和基因变异是否在相关个体之间显示相关传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ethical Issues in Genetic Epidemiology
This chapter reviews the breakthrough discovery of the complete sequence of human DNA in 2003, which rapidly ushered in an era of genomics and big data. It discusses “precision medicine,” which refers to the notion of accounting for individual variability in genes, environment, and lifestyle to devise new ways to prevent, detect, diagnose, and treat health conditions. It also describes “precision public health” as the related effort to use individual variability to more finely tailor preventive interventions for at-risk groups and improve population health. The chapter addresses scientific questions about the roles of genes, environmental, gene–gene, and gene–environment interactions in human health through the rigorous study of genotypic, phenotypic, and environmental data in human populations. It tackles the genomic contributions to health and disease, such as the assessment of whether diseases and gene variants show correlated transmission among related individuals.
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