抑郁症的遗传风险因素

T. Halldorsdottir, H. Hilmarsdóttir
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引用次数: 1

摘要

在过去十年中,对抑郁症遗传基础的研究取得了迅速进展。这一领域的研究为改善这种毁灭性疾病的诊断、预防和治疗提供了一条有希望的途径。本章的目的是回顾抑郁症的主要遗传和基因-环境相互作用的发现。我们首先描述了用于实证研究抑郁症家族聚集性的家庭和双胞胎研究。其次,我们对迄今为止发表的全基因组关联研究(GWAS)进行了综述。在GWAS研究结果的基础上,我们将讨论多基因风险评分在预测抑郁症中的应用。我们还回顾了最强大的候选基因研究和基因与环境相互作用的研究。最后,我们讨论了研究结果的临床意义和在该领域取得进一步进展的有希望的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic Risk Factors of Depression
Research on the genetic underpinnings of depression has rapidly advanced in the past decade. This field of research provides a promising avenue toward improving the diagnosis of, prevention of, and treatment for this devastating disorder. The goal of this chapter is to review the main genetic and gene-by-environment interaction findings on depression. We first describe family and twin studies used to empirically study the familial aggregation of depression. Second, we provide a review of the genome-wide association studies (GWAS) published to date. Building on GWAS findings, we will discuss the use of polygenic risk scores in predicting depression. We also review the most robust candidate gene studies and gene-by-environment interaction studies. Finally, we discuss the clinical implications of the findings and promising strategies for making further progress within this field.
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