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Relationship of Usual Volume and Heavy Consumption to Risk of Alcohol-Related Injury: Racial/Ethnic Disparities in Four U.S. National Alcohol Surveys.通常饮酒量和大量饮酒与酒精相关伤害风险的关系:美国四项全国酒精调查中的种族/族裔差异
J Stud Alcohol Drugs. 2016 Jan;77(1):58-67. doi: 10.15288/jsad.2016.77.58.
2
Gene expression changes in serotonin, GABA-A receptors, neuropeptides and ion channels in the dorsal raphe nucleus of adolescent alcohol-preferring (P) rats following binge-like alcohol drinking.暴饮式饮酒后,青春期酒精偏好(P)大鼠中缝背核中血清素、GABA-A受体、神经肽和离子通道的基因表达变化。
Pharmacol Biochem Behav. 2015 Feb;129:87-96. doi: 10.1016/j.pbb.2014.12.007. Epub 2014 Dec 24.
3
Racial/ethnic disparities in alcohol-related problems: differences by gender and level of heavy drinking.与酒精相关问题中的种族/民族差异:按性别和重度饮酒水平划分的差异
Alcohol Clin Exp Res. 2014 Jun;38(6):1662-70. doi: 10.1111/acer.12398. Epub 2014 Apr 14.
4
Stress and alcohol interactions: animal studies and clinical significance.应激与酒精相互作用:动物研究与临床意义。
Trends Neurosci. 2014 Apr;37(4):219-27. doi: 10.1016/j.tins.2014.02.006. Epub 2014 Mar 11.
5
The persistence of adolescent binge drinking into adulthood: findings from a 15-year prospective cohort study.青少年 binge drinking 持续至成年:一项为期 15 年的前瞻性队列研究结果。
BMJ Open. 2013 Aug 19;3(8):e003015. doi: 10.1136/bmjopen-2013-003015.
6
Gene-environment correlation: difficulties and a natural experiment-based strategy.基因-环境相关性:困难与基于自然实验的策略。
Am J Public Health. 2013 Oct;103 Suppl 1(Suppl 1):S167-73. doi: 10.2105/AJPH.2013.301415. Epub 2013 Aug 8.
7
Association, interaction, and replication analysis of genes encoding serotonin transporter and 5-HT3 receptor subunits A and B in alcohol dependence.基因编码 5-羟色胺转运体和 5-HT3 受体亚基 A 和 B 的关联、相互作用和复制分析与酒精依赖有关。
Hum Genet. 2013 Oct;132(10):1165-76. doi: 10.1007/s00439-013-1319-y. Epub 2013 Jun 12.
8
Addiction as a stress surfeit disorder.成瘾作为一种应激过度障碍。
Neuropharmacology. 2014 Jan;76 Pt B(0 0):370-82. doi: 10.1016/j.neuropharm.2013.05.024. Epub 2013 Jun 6.
9
A dual-process model of early substance use: tests in two diverse populations of adolescents.双过程模型在青少年早期物质使用中的应用:两个不同青少年群体的检验。
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10
Longitudinal relationship between drinking with peers, descriptive norms, and adolescent alcohol use.与同伴饮酒、描述性规范和青少年饮酒之间的纵向关系。
Prev Sci. 2014 Aug;15(4):497-505. doi: 10.1007/s11121-013-0391-9.

遗传、心理和人际网络因素与美国墨西哥裔青少年 2 年内 binge drinking 变化的相关性。

Genetic, Psychological, and Personal Network Factors Associated With Changes in Binge Drinking Over 2 Years Among Mexican Heritage Adolescents in the USA.

机构信息

Department of Healthy Living, Health Risk Prevention Team, Korea Health Promotion Institute, Jung-gu, Seoul, Republic of Korea.

Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

Ann Behav Med. 2019 Feb 1;53(2):126-137. doi: 10.1093/abm/kay019.

DOI:10.1093/abm/kay019
PMID:29697747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6200652/
Abstract

BACKGROUND

Despite prevalent binge drinking and alcohol-dependent symptoms among Hispanics, few studies have examined how multidimensional factors influence Hispanic adolescents' binge drinking. Purpose This study examines the effects of genetic, psychological, and social network factors on binge drinking over time among Mexican heritage adolescents in the USA and whether there are correlations among genetic variants that are associated with binge drinking and psychological and network characteristics.

METHODS

Mexican heritage adolescents (n = 731) participated in a longitudinal study, which included genetic testing at baseline, alcohol use assessments at first and second follow-ups, and questionnaires on sensation seeking, impulsivity, and peer and family network characteristics at second follow-up. Logistic regression and Spearman correlation analyses were performed.

RESULTS

After adjusting for demographic characteristics, underlying genetic clustering, and binge drinking at first follow-up, two genetic variants on tryptophan hydroxylase 2 (TPH2; rs17110451, rs7963717), sensation seeking and impulsivity, and having a greater fraction of peers who drink or encourage drinking alcohol were associated with greater risk whereas another genetic variant on TPH2 (rs11178999) and having a greater fraction of close family relationships were associated with reduced risk for binge drinking at second follow-up. Genetic variants in TPH1 (rs591556) were associated with sensation seeking and impulsivity, while genetic variants in TPH2 (rs17110451) were associated with the fraction of drinkers in family.

CONCLUSIONS

Results reveal that genetic variants in the serotonin pathway, behavioral disinhibition traits, and social networks exert joint influences on binge drinking in Mexican heritage adolescents in the USA.

摘要

背景

尽管西班牙裔人群普遍存在狂饮和酒精依赖症状,但很少有研究探讨多维因素如何影响西班牙裔青少年的狂饮行为。目的:本研究考察了遗传、心理和社交网络因素对美国墨西哥裔青少年随时间推移 binge drinking 的影响,以及与 binge drinking 相关的遗传变异与心理和网络特征之间是否存在相关性。

方法

墨西哥裔青少年(n=731)参与了一项纵向研究,该研究包括基线时的基因检测、第一次和第二次随访时的饮酒评估,以及第二次随访时的感觉寻求、冲动性以及同伴和家庭网络特征的问卷。进行了逻辑回归和 Spearman 相关分析。

结果

在调整了人口统计学特征、潜在的遗传聚类和第一次随访时的 binge drinking 后,色氨酸羟化酶 2(TPH2;rs17110451,rs7963717)上的两个遗传变异、感觉寻求和冲动性、以及有更多的同伴饮酒或鼓励饮酒的比例与更高的风险相关,而 TPH2 上的另一个遗传变异(rs11178999)和有更多的亲密家庭关系与第二次随访时 binge drinking 的风险降低相关。TPH1(rs591556)上的遗传变异与感觉寻求和冲动性相关,而 TPH2(rs17110451)上的遗传变异与家庭中饮酒者的比例相关。

结论

结果表明,血清素途径中的遗传变异、行为抑制特质和社交网络对美国墨西哥裔青少年 binge drinking 有共同影响。