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Common and specific genes and peripheral biomarkers in children and adults with attention-deficit/hyperactivity disorder.注意缺陷多动障碍儿童和成人的常见和特有基因及外周生物标志物。
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Neurosci Lett. 2017 Feb 3;639:88-93. doi: 10.1016/j.neulet.2016.12.068. Epub 2016 Dec 29.
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Cognitive Function of Children and Adolescents with Attention Deficit Hyperactivity Disorder and Learning Difficulties: A Developmental Perspective.注意缺陷多动障碍与学习困难儿童及青少年的认知功能:发展视角
Chin Med J (Engl). 2016 Aug 20;129(16):1922-8. doi: 10.4103/0366-6999.187861.
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Attention-deficit/hyperactivity disorder.注意缺陷多动障碍。
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Overview of Attention Deficit Hyperactivity Disorder in Young Children.幼儿注意力缺陷多动障碍概述
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Recurrent major depression and right hippocampal volume: A bivariate linkage and association study.复发性重度抑郁症与右侧海马体体积:双变量连锁与关联研究。
Hum Brain Mapp. 2016 Jan;37(1):191-202. doi: 10.1002/hbm.23025. Epub 2015 Oct 20.
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The muscarinic system, cognition and schizophrenia.毒蕈碱系统、认知与精神分裂症。
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注意缺陷多动障碍患者在连线测验中认知灵活性的遗传分析:从单核苷酸多态性、基因到通路水平。

Genetic analysis for cognitive flexibility in the trail-making test in attention deficit hyperactivity disorder patients from single nucleotide polymorphism, gene to pathway level.

机构信息

CAS Key Laboratory of Mental Health, Institute of Psychology , Beijing , China.

Department of Psychology, University of Chinese Academy of Sciences , Beijing , China.

出版信息

World J Biol Psychiatry. 2019 Jul;20(6):476-485. doi: 10.1080/15622975.2017.1386324. Epub 2017 Oct 25.

DOI:10.1080/15622975.2017.1386324
PMID:28971736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10752618/
Abstract

: Investigation of the genetic basis of endophenotype and analysis the pathways with multiple genes of small effects might increase the understanding of the genetic basis of attention deficit hyperactivity disorder (ADHD). Here we aimed to explore the genetic basis of cognitive flexibility in ADHD at the single nucleotide polymorphism (SNP), gene and pathway levels. The trail-making test was used to test the cognitive flexibility of 788 ADHD patients. A genome-wide association analysis of cognitive flexibility was conducted for 644,166 SNPs. : The top SNP rs2049161 ( = 5.08e-7) involved gene and the top gene in the gene-based analysis resulted in much literature evidence of associations with psychiatric disorders. Gene expression and network analysis showed their contribution to cognition function. The interval-enrichment analysis highlighted a potential contribution of 'adenylate cyclase activity' and to cognitive flexibility. Candidate pathway-based analysis for all SNPs found that glutamate system-, neurite outgrowth- and noradrenergic system-related pathways were significantly associated with cognitive flexibility (FDR <0.05), among which the neurite outgrowth pathway was also associated with ADHD symptoms. : This study provides evidence for the genes and pathways associated with cognitive flexibility and facilitate the uncovering of the genetic basis of ADHD.

摘要

探讨注意缺陷多动障碍(ADHD)的内表型遗传基础,并分析多个微效基因的途径,可能有助于加深对其遗传基础的理解。本研究旨在探讨 ADHD 患者在单核苷酸多态性(SNP)、基因和途径水平上认知灵活性的遗传基础。采用连线测验评估 788 例 ADHD 患者的认知灵活性。对 644166 个 SNP 进行了认知灵活性的全基因组关联分析。位于基因上的 top SNP rs2049161( = 5.08e-7)与基因相关,而在基因分析中,top 基因与精神障碍的关联有大量文献证据。基因表达和网络分析表明它们对认知功能有贡献。区间富集分析突出了“腺苷酸环化酶活性”和的潜在作用。对所有 SNP 的候选通路分析发现,谷氨酸系统、轴突生长和去甲肾上腺素能系统相关通路与认知灵活性显著相关(FDR <0.05),其中轴突生长通路也与 ADHD 症状相关。本研究为与认知灵活性相关的基因和途径提供了证据,有助于揭示 ADHD 的遗传基础。