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

机译:将精神疾病的多基因风险评分应用于患有双相情感障碍和重度抑郁症的大家庭

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摘要

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 (n ~ 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.
机译:人们认为精神病具有复杂的遗传病理,包括常见和罕见变异的相互作用。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,以突出显示常见遗传风险的模式。我们分析了大型谱系(n ~~ 260)中精神疾病的多基因风险评分,其中有30%的家庭成员患有重度抑郁症或躁郁症。研究分类交配和预期的模式,看来多基因风险的增加是由与家庭结婚的受影响个体造成的,导致世代相传的遗传风险增加。这可能解释了对情绪障碍的预期观察,由此发病更早,严重程度随着家庭的发展而增加。对罕见和常见变异进行联合分析可能是了解精神疾病家族遗传的有力方法。

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