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本文引用的文献

1
The Collaborative Study on the Genetics of Alcoholism.酒精中毒遗传学合作研究
Alcohol Health Res World. 1995;19(3):228-236.
2
Parental alcohol use disorder and offspring marital outcomes.父母的酒精使用障碍与子女的婚姻结局。
Addiction. 2019 Jan;114(1):81-91. doi: 10.1111/add.14405. Epub 2018 Sep 3.
3
Polygenic Risk Scores in Clinical Psychology: Bridging Genomic Risk to Individual Differences.多基因风险评分在临床心理学中的应用:连接基因组风险与个体差异。
Annu Rev Clin Psychol. 2018 May 7;14:119-157. doi: 10.1146/annurev-clinpsy-050817-084847.
4
Social Relationships Moderate Genetic Influences on Heavy Drinking in Young Adulthood.社会关系调节了遗传因素对青年期酗酒的影响。
J Stud Alcohol Drugs. 2017 Nov;78(6):817-826. doi: 10.15288/jsad.2017.78.817.
5
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.
6
Comparison of Parent, Peer, Psychiatric, and Cannabis Use Influences Across Stages of Offspring Alcohol Involvement: Evidence from the COGA Prospective Study.父母、同伴、精神疾病及大麻使用对后代酒精使用各阶段影响的比较:来自COGA前瞻性研究的证据
Alcohol Clin Exp Res. 2017 Feb;41(2):359-368. doi: 10.1111/acer.13293. Epub 2017 Jan 10.
7
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference.β-klotho基因(KLB)与饮酒有关,其基因产物β-klotho蛋白是成纤维细胞生长因子21(FGF21)调节酒精偏好所必需的。
Proc Natl Acad Sci U S A. 2016 Dec 13;113(50):14372-14377. doi: 10.1073/pnas.1611243113. Epub 2016 Nov 28.
8
Is marriage a buzzkill? A twin study of marital status and alcohol consumption.婚姻是扫兴之事吗?一项关于婚姻状况与酒精消费的双胞胎研究。
J Fam Psychol. 2016 Sep;30(6):698-707. doi: 10.1037/fam0000221. Epub 2016 Jun 23.
9
Effect of Marriage on Risk for Onset of Alcohol Use Disorder: A Longitudinal and Co-Relative Analysis in a Swedish National Sample.婚姻对酒精使用障碍发病风险的影响:瑞典全国样本的纵向和相关性分析
Am J Psychiatry. 2016 Sep 1;173(9):911-8. doi: 10.1176/appi.ajp.2016.15111373. Epub 2016 May 16.
10
Epidemiology of DSM-5 Alcohol Use Disorder: Results From the National Epidemiologic Survey on Alcohol and Related Conditions III.《精神疾病诊断与统计手册》第五版酒精使用障碍的流行病学:来自酒精及相关状况全国流行病学调查三期的结果
JAMA Psychiatry. 2015 Aug;72(8):757-66. doi: 10.1001/jamapsychiatry.2015.0584.

采用发展的观点,在一个风险较高的成年样本中,研究婚姻对重度饮酒的调节作用。

Using a developmental perspective to examine the moderating effects of marriage on heavy episodic drinking in a young adult sample enriched for risk.

机构信息

Department of Psychology, Pusan National University, Busan, South Korea.

Department of Psychology, Virginia Commonwealth University, Richmond, VA, USA.

出版信息

Dev Psychopathol. 2021 Aug;33(3):1097-1106. doi: 10.1017/S0954579420000371.

DOI:10.1017/S0954579420000371
PMID:32611468
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7775899/
Abstract

Many studies demonstrate that marriage protects against risky alcohol use and moderates genetic influences on alcohol outcomes; however, previous work has not considered these effects from a developmental perspective or in high-risk individuals. These represent important gaps, as it cannot be assumed that marriage has uniform effects across development or in high-risk samples. We took a longitudinal developmental approach to examine whether marital status was associated with heavy episodic drinking (HED), and whether marital status moderated polygenic influences on HED. Our sample included 937 individuals (53.25% female) from the Collaborative Study on the Genetics of Alcoholism who reported their HED and marital status biennially between the ages of 21 and 25. Polygenic risk scores (PRS) were derived from a genome-wide association study of alcohol consumption. Marital status was not associated with HED; however, we observed pathogenic gene-by-environment effects that changed across young adulthood. Among those who married young (age 21), individuals with higher PRS reported more HED; however, these effects decayed over time. The same pattern was found in supplementary analyses using parental history of alcohol use disorder as the index of genetic liability. Our findings indicate that early marriage may exacerbate risk for those with higher polygenic load.

摘要

许多研究表明,婚姻可以预防危险的饮酒行为,并调节遗传因素对酒精相关结果的影响;然而,之前的研究尚未从发展的角度或在高风险个体中考虑这些影响。这些都是重要的空白,因为不能假设婚姻在整个发展过程中或在高风险样本中具有统一的效果。我们采取了纵向发展的方法来研究婚姻状况是否与重度饮酒(HED)有关,以及婚姻状况是否调节了 HED 的多基因影响。我们的样本包括来自酒精遗传合作研究的 937 名个体(53.25%为女性),他们在 21 至 25 岁之间每两年报告一次 HED 和婚姻状况。多基因风险评分(PRS)是从一项关于饮酒的全基因组关联研究中得出的。婚姻状况与 HED 无关;然而,我们观察到在整个成年早期发生变化的致病性基因-环境相互作用。在那些早婚(21 岁)的人中,PRS 较高的个体报告了更多的 HED;然而,这些影响随着时间的推移而减弱。在使用父母的酒精使用障碍史作为遗传易感性指标的补充分析中也发现了同样的模式。我们的研究结果表明,对于那些多基因负荷较高的人来说,早期婚姻可能会加剧风险。

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