University of Missouri,Columbia, MO,USA.
QIMR Berghofer,Brisbane, Queensland,Australia.
Psychol Med. 2019 Jul;49(10):1705-1712. doi: 10.1017/S0033291718002325. Epub 2018 Aug 30.
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.
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.
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.
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.
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。
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。
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。
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。