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将精神疾病的多基因风险评分应用于一个患有双相情感障碍和重度抑郁症的大家庭。

Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder.

作者信息

de Jong Simone, Diniz Mateus Jose Abdalla, Saloma Andiara, Gadelha Ary, Santoro Marcos L, Ota Vanessa K, Noto Cristiano, Curtis Charles, Newhouse Stephen J, Patel Hamel, Hall Lynsey S, O Reilly Paul F, Belangero Sintia I, Bressan Rodrigo A, Breen Gerome

机构信息

MRC Social Genetic and Developmental Psychiatry Centre, Institute of Psychiatry Psychology and Neuroscience, King's College London, London, SE5 8AF, UK.

National Institute of Health Research Biomedical Research Centre for Mental Health, Maudsley Hospital and Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, SE5 8AF, UK.

出版信息

Commun Biol. 2018 Oct 8;1:163. doi: 10.1038/s42003-018-0155-y. eCollection 2018.

Abstract

Psychiatric disorders are thought to have a complex genetic pathology consisting of interplay of common and rare variation. Traditionally, pedigrees are used to shed light on the latter only, while here we discuss the application of polygenic risk scores to also highlight patterns of common genetic risk. We analyze polygenic risk scores for psychiatric disorders in a large pedigree ( ~ 260) in which 30% of family members suffer from major depressive disorder or bipolar disorder. Studying patterns of assortative mating and anticipation, it appears increased polygenic risk is contributed by affected individuals who married into the family, resulting in an increasing genetic risk over generations. This may explain the observation of anticipation in mood disorders, whereby onset is earlier and the severity increases over the generations of a family. Joint analyses of rare and common variation may be a powerful way to understand the familial genetics of psychiatric disorders.

摘要

精神疾病被认为具有复杂的遗传病理学,由常见变异和罕见变异的相互作用组成。传统上,系谱仅用于阐明后者,而在此我们讨论多基因风险评分的应用,以突出常见遗传风险模式。我们在一个大型系谱(约260人)中分析了精神疾病的多基因风险评分,其中30%的家庭成员患有重度抑郁症或双相情感障碍。研究选型交配和遗传早现模式时发现,与家族成员结婚的患病个体导致多基因风险增加,从而使几代人的遗传风险不断上升。这可能解释了在情绪障碍中观察到的遗传早现现象,即一个家族几代人中发病年龄提前且病情严重程度增加。对罕见变异和常见变异进行联合分析可能是理解精神疾病家族遗传学的有效方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b537/6175827/824fb3303c55/42003_2018_155_Fig1_HTML.jpg

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