从跨诊断多基因风险评分中识别儿童情绪障碍:一项儿童和青少年的研究。

E. Barnett, J. Biederman, A. Doyle, J. Hess, M. DiSalvo, S. Faraone
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引用次数: 2

摘要

目的:情绪障碍通常与注意缺陷/多动障碍(ADHD)、破坏性行为障碍(DBDs)和攻击行为共存。我们的目的是确定基于这些疾病的外部全基因组关联研究(GWASs)的多基因风险评分(prs)是否可以改善情绪障碍的遗传鉴定。方法:我们结合了6个独立的家庭研究,这些研究有基因数据,并使用不同版本的《精神障碍诊断与统计手册》(DSM)对情绪障碍进行诊断。我们通过对ADHD、ADHD合并DBD、重度抑郁障碍(MDD)、双相情感障碍(BPD)和攻击行为的GWASs汇总统计计算PRSs,确定了6 - 17岁参与者的并发或未来情绪障碍。结果:在我们的485名青少年样本中,356名(73%)发展为阈下或完全情绪障碍,129名(27%)没有。对于识别任何情绪障碍参与者的7个模型,交叉验证的受试者工作特征曲线(auc)下的平均面积范围从年龄和性别基本模型的0.552到基本模型+所有5个PRSs的0.648。当单独纳入基础模型时,ADHD PRS (OR = 1.65, P < .001)、攻击性PRS (OR = 1.27, P = .02)和MDD PRS (OR = 1.23, P = .047)与任何情绪障碍的发展均显著相关。结论:使用PRSs治疗ADHD、MDD、BPD、dbd和攻击性,我们可以适度地识别情绪障碍的存在。这些发现扩展了精神疾病的跨诊断遗传成分的证据,并证明使用传统诊断边界计算的PRSs在跨诊断框架内是有用的。
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Identifying Pediatric Mood Disorders From Transdiagnostic Polygenic Risk Scores: A Study of Children and Adolescents.
Objective: Mood disorders often co-occur with attention-deficit/hyperactive disorder (ADHD), disruptive behavior disorders (DBDs), and aggression. We aimed to determine if polygenic risk scores (PRSs) based on external genome-wide association studies (GWASs) of these disorders could improve genetic identification of mood disorders. Methods: We combined 6 independent family studies that had genetic data and diagnoses for mood disorders that were made using different editions of the Diagnostic and Statistical Manual of Mental Disorders (DSM). We identified mood disorders, either concurrently or in the future, in participants between 6 and 17 years of age using PRSs calculated using summary statistics of GWASs for ADHD, ADHD with DBD, major depressive disorder (MDD), bipolar disorder (BPD), and aggression to compute PRSs. Results: In our sample of 485 youths, 356 (73%) developed a subthreshold or full mood disorder and 129 (27%) did not. The cross-validated mean areas under the receiver operating characteristic curve (AUCs) for the 7 models identifying participants with any mood disorder ranged from 0.552 in the base model of age and sex to 0.648 in the base model + all 5 PRSs. When included in the base model individually, the ADHD PRS (OR = 1.65, P < .001), Aggression PRS (OR = 1.27, P = .02), and MDD PRS (OR = 1.23, P = .047) were significantly associated with the development of any mood disorder. Conclusions: Using PRSs for ADHD, MDD, BPD, DBDs, and aggression, we could modestly identify the presence of mood disorders. These findings extend evidence for transdiagnostic genetic components of psychiatric illness and demonstrate that PRSs calculated using traditional diagnostic boundaries can be useful within a transdiagnostic framework.
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Emerging Perspectives in Addiction Psychiatry. Emerging Therapies for Attention-Deficit/Hyperactivity Disorder Charles Bowden, MD, 1938-2022. In Memoriam: Jan Fawcett, MD, 1934-2022. The Relationship Between Mental Pain, Suicide Risk, and Childhood Traumatic Experiences: Results From a Multicenter Study.
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