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首页> 外文期刊>American journal of psychiatry >High loading of polygenic risk for ADHD in children with comorbid aggression
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High loading of polygenic risk for ADHD in children with comorbid aggression

机译:高发性合并症儿童多动症多基因风险的负荷

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Objective: Although attention deficit hyperactivity disorder (ADHD) is highly heritable, genome-wide association studies (GWAS) have not yet identified any common genetic variants that contribute to risk. There is evidence that aggression or conduct disorder in children with ADHD indexes higher genetic loading and clinical severity. The authors examine whether common genetic variants considered en masse as polygenic scores for ADHD are especially enriched in children with comorbid conduct disorder. Method: Polygenic scores derived from an ADHD GWAS meta-analysis were calculated in an independent ADHD sample (452 case subjects, 5,081 comparison subjects). Multivariate logistic regression analyses were employed to compare polygenic scores in the ADHD and comparison groups and test for higher scores in ADHD case subjects with comorbid conduct disorder relative to comparison subjects and relative to those without comorbid conduct disorder. Association with symptom scores was tested using linear regression. Results: Polygenic risk for ADHD, derived from the meta-analysis, was higher in the independent ADHD group than in the comparison group. Polygenic score was significantly higher in ADHD case subjects with conduct disorder relative to ADHD case subjects without conduct disorder. ADHD polygenic score showed significant association with comorbid conduct disorder symptoms. This relationship was explained by the aggression items. Conclusions: Common genetic variation is relevant to ADHD, especially in individuals with comorbid aggression. The findings suggest that the previously published ADHD GWAS meta-analysis contains weak but true associations with common variants, support for which falls below genome-wide significance levels. The findings also highlight the fact that aggression in ADHD indexes genetic as well as clinical severity.
机译:目的:尽管注意力缺陷多动障碍(ADHD)是高度可遗传的,但全基因组关联研究(GWAS)尚未发现任何导致风险的常见遗传变异。有证据表明,患有ADHD的儿童的攻击性或品行障碍具有更高的遗传负荷和临床严重性。作者检查了被普遍视为多动症多基因评分的常见遗传变异在患有合并症的儿童中是否特别丰富。方法:在独立的ADHD样本(452例受试者,5,081个比较受试者)中计算从ADHD GWAS荟萃分析得出的多基因评分。采用多因素logistic回归分析比较ADHD和对照组的多基因评分,并测试患有共病行为障碍的ADHD病例受试者相对于比较受试者和相对于没有共病行为障碍的受试者的较高得分。使用线性回归测试与症状评分的关联。结果:荟萃分析得出的多动症多基因风险在独立的多动症组中高于对照组。与没有行为障碍的ADHD案例受试者相比,有行为障碍的ADHD案例受试者的多基因得分明显更高。多动症多基因评分显示与共病行为障碍症状显着相关。侵略性项目解释了这种关系。结论:常见的遗传变异与多动症有关,特别是在合并症患者中。研究结果表明,先前发表的ADHD GWAS荟萃分析包含与常见变体的微弱但真实的关联,对这些变异的支持低于全基因组显着性水平。这些发现还凸显了多动症的侵袭性标志着遗传和临床严重性。

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