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本文引用的文献

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Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort.基于 UK Biobank 队列的全基因组分析自我报告的冒险行为和跨疾病遗传相关性。
Transl Psychiatry. 2018 Feb 2;8(1):39. doi: 10.1038/s41398-017-0079-1.
2
Psychiatric Genomics: An Update and an Agenda.精神科基因组学:最新进展与议程
Am J Psychiatry. 2018 Jan 1;175(1):15-27. doi: 10.1176/appi.ajp.2017.17030283. Epub 2017 Oct 3.
3
The intergenerational transmission of at-risk/problem gambling: The moderating role of parenting practices.高危/问题赌博的代际传递:养育方式的调节作用。
Am J Addict. 2017 Oct;26(7):707-712. doi: 10.1111/ajad.12599. Epub 2017 Sep 7.
4
Embracing polygenicity: a review of methods and tools for psychiatric genetics research.拥抱多基因性:精神遗传学研究方法和工具述评。
Psychol Med. 2018 May;48(7):1055-1067. doi: 10.1017/S0033291717002318. Epub 2017 Aug 29.
5
Leveraging Genomic Data in Smoking Cessation Trials in the Era of Precision Medicine: Why and How.利用精准医学时代的基因组数据进行戒烟临床试验:原因与方法。
Nicotine Tob Res. 2018 Mar 6;20(4):414-424. doi: 10.1093/ntr/ntx097.
6
Genetic and environmental origins of gambling behaviors from ages 18 to 25: A longitudinal twin family study.18至25岁赌博行为的遗传和环境起源:一项纵向双胞胎家庭研究。
Psychol Addict Behav. 2017 May;31(3):367-374. doi: 10.1037/adb0000266.
7
Genome-wide association study of pathological gambling.病态赌博的全基因组关联研究。
Eur Psychiatry. 2016 Aug;36:38-46. doi: 10.1016/j.eurpsy.2016.04.001. Epub 2016 Jun 14.
8
The Fourth Law of Behavior Genetics.行为遗传学第四定律。
Curr Dir Psychol Sci. 2015 Jul 1;24(4):304-312. doi: 10.1177/0963721415580430.
9
The Value of Direct Replication.直接复制的价值。
Perspect Psychol Sci. 2014 Jan;9(1):76-80. doi: 10.1177/1745691613514755.
10
Local area disadvantage and gambling involvement and disorder: Evidence for gene-environment correlation and interaction.局部地区劣势与赌博参与及障碍:基因-环境相关性与相互作用的证据。
J Abnorm Psychol. 2015 Aug;124(3):606-22. doi: 10.1037/abn0000071.

遗传和环境因素对赌博障碍易感性的影响:两项双胞胎研究的复制和合并分析。

Genetic and environmental influences on gambling disorder liability: a replication and combined analysis of two twin studies.

机构信息

University of Missouri,Columbia, MO,USA.

QIMR Berghofer,Brisbane, Queensland,Australia.

出版信息

Psychol Med. 2019 Jul;49(10):1705-1712. doi: 10.1017/S0033291718002325. Epub 2018 Aug 30.

DOI:10.1017/S0033291718002325
PMID:30160223
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6395556/
Abstract

BACKGROUND

Gambling disorder (GD), recognized in Diagnostic and Statistical Manual of Mental Disorders, Version 5 (DSM-5) as a behavioral addiction, is associated with a range of adverse outcomes. However, there has been little research on the genetic and environmental influences on the development of this disorder. This study reports results from the largest twin study of GD conducted to date.

METHODS

Replication and combined analyses were based on samples of 3292 (mean age 31.8, born 1972-79) and 4764 (mean age 37.7, born 1964-71) male, female, and unlike-sex twin pairs from the Australian Twin Registry. Univariate biometric twin models estimated the proportion of variation in the latent GD liability that could be attributed to genetic, shared environmental, and unique environmental factors, and whether these differed quantitatively or qualitatively for men and women.

RESULTS

In the replication study, when using a lower GD threshold, there was evidence for significant genetic (60%; 95% confidence interval (CI) 45-76%) and unique environmental (40%; 95% CI 24-56%), but not shared environmental contributions (0%; 95% CI 0-0%) to GD liability; this did not significantly differ from the original study. In the combined analysis, higher GD thresholds (such as one consistent with DSM-5 GD) and a multiple threshold definitions of GD yielded similar results. There was no evidence for quantitative or qualitative sex differences in the liability for GD.

CONCLUSIONS

Twin studies of GD are few in number but they tell a remarkably similar story: substantial genetic and unique environmental influences, with no evidence for shared environmental contributions or sex differences in GD liability.

摘要

背景

赌博障碍(GD),在《精神障碍诊断与统计手册》第五版(DSM-5)中被认定为一种行为成瘾,与一系列不良后果相关。然而,对于这种障碍的发展的遗传和环境影响的研究甚少。本研究报告了迄今为止针对 GD 进行的最大双胞胎研究的结果。

方法

基于来自澳大利亚双胞胎登记处的 3292 对(平均年龄 31.8 岁,出生于 1972-79 年)和 4764 对(平均年龄 37.7 岁,出生于 1964-71 年)男性、女性和非同性别双胞胎的样本进行了复制和综合分析。单变量生物计量双胞胎模型估计了潜在 GD 倾向的变异中可以归因于遗传、共享环境和独特环境因素的比例,以及这些因素在男性和女性之间是否在数量或质量上有所不同。

结果

在复制研究中,当使用较低的 GD 阈值时,GD 倾向存在显著的遗传(60%;95%置信区间[CI] 45-76%)和独特环境(40%;95%CI 24-56%)但无共享环境(0%;95%CI 0-0%)贡献;这与原始研究没有显著差异。在综合分析中,较高的 GD 阈值(例如与 DSM-5 GD 一致的阈值)和 GD 的多个阈值定义得出了相似的结果。GD 倾向没有证据表明存在定量或定性的性别差异。

结论

GD 的双胞胎研究数量较少,但它们讲述了一个惊人相似的故事:遗传和独特环境的影响很大,没有证据表明 GD 倾向存在共享环境贡献或性别差异。