ADHD的遗传结构与其他精神疾病和与认知相关的表型重叠
M Ribasés1, M Mitjans2, C A Hartman3
1Department of Mental Health, Hospital Universitari Vall d'Hebron, Barcelona, Spain; Psychiatric Genetics Unit, Group of Psychiatry, Mental Health and Addiction, Vall d'Hebron Research Institute (VHIR), Universitat Autònoma de Barcelona, Barcelona, Spain; Biomedical Network Research Centre on Mental Health (CIBERSAM), Barcelona, Spain; Department of Genetics, Microbiology, and Statistics, Faculty of Biology, Universitat de Barcelona, Barcelona, Spain.
遗传因素显著影响注意力缺陷/多动症障碍 (ADHD) 的并发症. 虽然双胞胎研究显示了大量的重叠,但全基因组数据显示了较小的效应和复杂的,有时是双向的,ADHD和其他疾病之间的因果关系.
科学领域:
- 精神病学是一个精神病学.
- 遗传学 遗传学是一种遗传学.
- 行为科学 行为科学
背景情况:
- 注意缺陷/多动障碍 (ADHD) 经常与其他精神疾病和特征同时发生.
- 了解这些并发症的遗传基础对于全面的精神病治疗至关重要.
研究的目的:
- 审查和解释有关ADHD并发症遗传结构的现有文献.
- 综合从定量和分子遗传研究的发现.
主要方法:
- 对定量遗传研究 (例如双胞胎研究) 的审查.
- 分析分子遗传数据,包括全基因组关联研究 (GWAS) 和多基因风险评分.
- 对遗传数据进行因果推理的检查.
主要成果:
- 定量遗传研究表明,遗传因素在ADHD并发症中起着重要的作用.
- 分子遗传相关性证实了这一模式,但与双胞胎研究相比,其效果大小较小.
- 最初的基因分析支持ADHD和并发性疾病之间的因果关系,有一些证据表明双向影响.
结论:
- ADHD与其他精神疾病的同时发生是基因可解释的.
- 需要使用全基因组方法进行进一步的研究,以确定特定的遗传变异和途径.
- 在ADHD和其常见的并发症之间存在复杂,潜在的双向,遗传关系.
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