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本文引用的文献

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Antisocial peer affiliation and externalizing disorders: Evidence for Gene × Environment × Development interaction.反社会同伴关系与外化障碍:基因×环境×发展相互作用的证据。
Dev Psychopathol. 2017 Feb;29(1):155-172. doi: 10.1017/S0954579416000109. Epub 2016 Feb 24.
2
A Genome-Wide Association Study of a Biomarker of Nicotine Metabolism.一项关于尼古丁代谢生物标志物的全基因组关联研究。
PLoS Genet. 2015 Sep 25;11(9):e1005498. doi: 10.1371/journal.pgen.1005498. eCollection 2015.
3
Meta-analysis of six genes (BDNF, DRD1, DRD3, DRD4, GRIN2B and MAOA) involved in neuroplasticity and the risk for alcohol dependence.对涉及神经可塑性和酒精依赖风险的六个基因(脑源性神经营养因子、多巴胺受体D1、多巴胺受体D3、多巴胺受体D4、谷氨酸受体亚基2B和单胺氧化酶A)的荟萃分析。
Drug Alcohol Depend. 2015 Apr 1;149:259-63. doi: 10.1016/j.drugalcdep.2015.01.017. Epub 2015 Jan 24.
4
Candidate gene-environment interaction research: reflections and recommendations.候选基因-环境相互作用研究:思考与建议。
Perspect Psychol Sci. 2015 Jan;10(1):37-59. doi: 10.1177/1745691614556682.
5
Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans.美国人群尼古丁依赖的全基因组关联研究:非裔美国人和欧裔美国人中新型风险位点的鉴定
Biol Psychiatry. 2015 Mar 1;77(5):493-503. doi: 10.1016/j.biopsych.2014.08.025. Epub 2014 Sep 16.
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Personality and Psychopathology: A Stagnant Field in Need of Development.人格与精神病理学:一个亟待发展的停滞领域。
Eur J Pers. 2014 Jul 1;28(4):362-386. doi: 10.1002/per.1962.
7
The hidden efficacy of interventions: gene×environment experiments from a differential susceptibility perspective.干预措施的潜在功效:从易感性差异的角度看基因×环境实验。
Annu Rev Psychol. 2015 Jan 3;66:381-409. doi: 10.1146/annurev-psych-010814-015407. Epub 2014 Aug 11.
8
Gene-environment interplay between parent-child relationship problems and externalizing disorders in adolescence and young adulthood.青春期和成年早期亲子关系问题与外化性障碍之间的基因-环境相互作用。
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General and specific predictors of nicotine and alcohol dependence in early adulthood: genetic and environmental influences.成年早期尼古丁和酒精依赖的一般及特定预测因素:遗传和环境影响
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A meta-analytic evaluation of the endophenotype hypothesis: effects of measurement paradigm in the psychiatric genetics of impulsivity.对内表型假说的荟萃分析评估:测量范式在冲动性精神遗传学中的作用
J Abnorm Psychol. 2014 Aug;123(3):660-75. doi: 10.1037/a0037094. Epub 2014 Jun 30.

一种针对成瘾和外化性障碍候选基因研究的测试-重复方法:五项纵向研究的合作

A Test-Replicate Approach to Candidate Gene Research on Addiction and Externalizing Disorders: A Collaboration Across Five Longitudinal Studies.

作者信息

Samek Diana R, Bailey Jennifer, Hill Karl G, Wilson Sylia, Lee Susanne, Keyes Margaret A, Epstein Marina, Smolen Andrew, Miller Michael, Winters Ken C, Hawkins J David, Catalano Richard F, Iacono William G, McGue Matt

机构信息

Department of Human Development and Family Studies, Auburn University, 203 Spidle Hall, Auburn, AL, 36849, USA.

School of Social Work, University of Washington, Seattle, WA, USA.

出版信息

Behav Genet. 2016 Sep;46(5):608-626. doi: 10.1007/s10519-016-9800-8. Epub 2016 Jul 21.

DOI:10.1007/s10519-016-9800-8
PMID:27444553
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5060092/
Abstract

This study presents results from a collaboration across five longitudinal studies seeking to test and replicate models of gene-environment interplay in the development of substance use and externalizing disorders (SUDs, EXT). We describe an overview of our conceptual models, plan for gene-environment interplay analyses, and present main effects results evaluating six candidate genes potentially relevant to SUDs and EXT (MAOA, 5-HTTLPR, COMT, DRD2, DAT1, and DRD4). All samples included rich longitudinal and phenotypic measurements from childhood/adolescence (ages 5-13) through early adulthood (ages 25-33); sample sizes ranged from 3487 in the test sample, to ~600-1000 in the replication samples. Phenotypes included lifetime symptom counts of SUDs (nicotine, alcohol and cannabis), adult antisocial behavior, and an aggregate externalizing disorder composite. Covariates included the first 10 ancestral principal components computed using all autosomal markers in subjects across the data sets, and age at the most recent assessment. Sex, ancestry, and exposure effects were thoroughly evaluated. After correcting for multiple testing, only one significant main effect was found in the test sample, but it was not replicated. Implications for subsequent gene-environment interplay analyses are discussed.

摘要

本研究展示了五项纵向研究合作得出的结果,这些研究旨在测试和复制物质使用障碍和外化性障碍(SUDs,EXT)发展过程中基因-环境相互作用的模型。我们描述了概念模型的概述、基因-环境相互作用分析计划,并呈现了评估六个可能与SUDs和EXT相关的候选基因(MAOA、5-HTTLPR、COMT、DRD2、DAT1和DRD4)的主效应结果。所有样本都包含从童年/青少年期(5至13岁)到成年早期(25至33岁)丰富的纵向和表型测量数据;样本量从测试样本中的3487人到复制样本中的约600至1000人不等。表型包括SUDs(尼古丁、酒精和大麻)的终生症状计数、成人反社会行为以及外化性障碍综合指标。协变量包括使用数据集中所有常染色体标记计算得出的前10个祖先主成分,以及最近一次评估时的年龄。对性别、血统和暴露效应进行了全面评估。在进行多重检验校正后,测试样本中仅发现一个显著的主效应,但未得到复制。文中讨论了对后续基因-环境相互作用分析的启示。