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Studying individual risk factors for self-harm in the UK Biobank: A polygenic scoring and Mendelian randomisation study

机译:研究英国生物伤害的个人风险因素:一种多种子基评分和孟德尔随机化研究

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Background Identifying causal risk factors for self-harm is essential to inform preventive interventions. Epidemiological studies have identified risk factors associated with self-harm, but these associations can be subject to confounding. By implementing genetically informed methods to better account for confounding, this study aimed to better identify plausible causal risk factors for self-harm. Methods and findings Using summary statistics from 24 genome-wide association studies (GWASs) comprising 16,067 to 322,154 individuals, polygenic scores (PSs) were generated to index 24 possible individual risk factors for self-harm (i.e., mental health vulnerabilities, substance use, cognitive traits, personality traits, and physical traits) among a subset of UK Biobank participants (N = 125,925, 56.2% female) who completed an online mental health questionnaire in the period from 13 July 2016 to 27 July 2017. In total, 5,520 (4.4%) of these participants reported having self-harmed in their lifetime. In binomial regression models, PSs indexing 6 risk factors (major depressive disorder [MDD], attention deficit/hyperactivity disorder [ADHD], bipolar disorder, schizophrenia, alcohol dependence disorder, and lifetime cannabis use) predicted self-harm, with effect sizes ranging from odds ratio (OR) = 1.05 (95% CI 1.02 to 1.07, q = 0.008) for lifetime cannabis use to OR = 1.20 (95% CI 1.16 to 1.23, q = 1.33 × 10?35) for MDD. No systematic differences emerged between suicidal and non-suicidal self-harm. To further probe causal relationships, two-sample Mendelian randomisation (MR) analyses were conducted, with MDD, ADHD, and schizophrenia emerging as the most plausible causal risk factors for self-harm. The genetic liabilities for MDD and schizophrenia were associated with self-harm independently of diagnosis and medication. Main limitations include the lack of representativeness of the UK Biobank sample, that self-harm was self-reported, and the limited power of some of the included GWASs, potentially leading to possible type II error. Conclusions In addition to confirming the role of MDD, we demonstrate that ADHD and schizophrenia likely play a role in the aetiology of self-harm using multivariate genetic designs for causal inference. Among the many individual risk factors we simultaneously considered, our findings suggest that systematic detection and treatment of core psychiatric symptoms, including psychotic and impulsivity symptoms, may be beneficial among people at risk for self-harm.
机译:背景技术识别自我危害因果危险因素对于通知预防性干预措施至关重要。流行病学研究已经确定了与自我危害相关的风险因素,但这些协会可能受到混淆。通过实施转基础知识的方法来更好地解释混淆,这项研究旨在更好地识别自我伤害的合理因果危险因素。使用16,067至322,154个个体的24种基因组关联研究(GWASS)的方法和结果,产生多种子学分数(PSS),以指数24个体危险因素(即精神健康脆弱性,物质使用,在2016年7月13日至2017年7月27日,英国Biobank参与者的子集(N = 125,925,56.2%的女性)中的认知特征和身体特征)在2016年7月13日至27日。总,5,520( 4.4%)这些参与者报告在其终生中自我伤害。在二项式回归模型中,PSS索引6危险因素(重大抑郁症[MDD],注意力/多动障碍[ADHD],双相情感障碍,精神分裂症,酒精依赖障碍和寿命大麻使用)预测自伤,效果大小测量从少数(或)= 1.05(95%CI 1.02至1.07,q = 0.008),用于MDD的寿命大麻的寿命大麻使用或= 1.20(95%CI 1.16至1.23,q = 1.33×10?35)。自杀和非自杀性自我危害之间没有产生系统的差异。为了进一步探测因果关系,用MDD,ADHD和精神分裂症进行两样的孟德尔随机化(MR)分析作为自我伤害最合理的因果危险因素。 MDD和精神分裂症的遗传责任与独立于诊断和药物的自我伤害有关。主要限制包括英国Biobank样本的代表性,即自我报告的自我危害,以及一些包括的GWAS的有限力量,可能导致II型错误。结论除了确认MDD的作用外,我们证明ADHD和精神分裂症可能在使用多元遗传设计进行因果推断的自我危害中发挥作用。在我们同时考虑的许多个人风险因素中,我们的研究结果表明,系统的检测和治疗核心精神症状,包括精神病症状,可能是自我危害风险的人们中有益。

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