MRC Integrative Epidemiology Unit (IEU), University of Bristol, Bristol, United Kingdom.
Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
PLoS Genet. 2020 May 11;16(5):e1008185. doi: 10.1371/journal.pgen.1008185. eCollection 2020 May.
Psychiatric disorders are highly heritable and associated with a wide variety of social adversity and physical health problems. Using genetic liability (rather than phenotypic measures of disease) as a proxy for psychiatric disease risk can be a useful alternative for research questions that would traditionally require large cohort studies with long-term follow up. Here we conducted a hypothesis-free phenome-wide association study in about 330,000 participants from the UK Biobank to examine associations of polygenic risk scores (PRS) for five psychiatric disorders (major depression (MDD), bipolar disorder (BP), schizophrenia (SCZ), attention-deficit/ hyperactivity disorder (ADHD) and autism spectrum disorder (ASD)) with 23,004 outcomes in UK Biobank, using the open-source PHESANT software package. There was evidence after multiple testing (p<2.55x10-06) for associations of PRSs with 294 outcomes, most of them attributed to associations of PRSMDD (n = 167) and PRSSCZ (n = 157) with mental health factors. Among others, we found strong evidence of association of higher PRSADHD with 1.1 months younger age at first sexual intercourse [95% confidence interval [CI]: -1.25,-0.92] and a history of physical maltreatment; PRSASD with 0.01% lower erythrocyte distribution width [95%CI: -0.013,-0.007]; PRSSCZ with 0.95 lower odds of playing computer games [95%CI:0.95,0.96]; PRSMDD with a 0.12 points higher neuroticism score [95%CI:0.111,0.135] and PRSBP with 1.03 higher odds of having a university degree [95%CI:1.02,1.03]. We were able to show that genetic liabilities for five major psychiatric disorders associate with long-term aspects of adult life, including socio-demographic factors, mental and physical health. This is evident even in individuals from the general population who do not necessarily present with a psychiatric disorder diagnosis.
精神障碍的遗传性很强,与各种社会逆境和身体健康问题有关。使用遗传易感性(而不是疾病的表型测量)作为精神疾病风险的替代指标,可以用于研究传统上需要长期随访的大型队列研究的问题。在这里,我们使用开源 PHESANT 软件包,在英国生物银行的约 33 万名参与者中进行了一项无假设的全基因组关联研究,以检查五种精神障碍(重度抑郁症(MDD)、双相情感障碍(BP)、精神分裂症(SCZ)、注意缺陷/多动障碍(ADHD)和自闭症谱系障碍(ASD))的多基因风险评分(PRS)与英国生物银行 23004 个结果之间的关联。在进行多次测试后(p<2.55x10-06),PRS 与 294 个结果之间存在关联,其中大多数归因于 PRSMDD(n = 167)和 PRSSCZ(n = 157)与心理健康因素之间的关联。除此之外,我们还发现了强有力的证据表明,较高的 PRSADHD 与首次性行为的年龄提前 1.1 个月有关[95%置信区间[CI]:-1.25,-0.92]和遭受身体虐待的历史;PRSASD 与红细胞分布宽度降低 0.01%有关[95%CI:-0.013,-0.007];PRSSCZ 与玩电脑游戏的可能性降低 0.95%有关[95%CI:0.95,0.96];PRSMDD 与神经质评分高 0.12 分有关[95%CI:0.111,0.135],PRSBP 与获得大学学位的可能性增加 1.03 有关[95%CI:1.02,1.03]。我们能够表明,五种主要精神障碍的遗传易感性与成年期的长期方面相关,包括社会人口因素、心理和身体健康。即使在不一定患有精神障碍诊断的普通人群个体中,也可以看到这种情况。