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健康政策与遗传禀赋:理解对法定最低饮酒年龄法律的反应来源。

Health policy and genetic endowments: Understanding sources of response to Minimum Legal Drinking Age laws.

机构信息

La Follette School of Public Affairs, Department of Sociology, Center for Demography of Health and Aging, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Department of Biostatistics and Medical Informatics, Center for Demography of Health and Aging, University of Wisconsin-Madison, Madison, Wisconsin, USA.

出版信息

Health Econ. 2021 Jan;30(1):194-203. doi: 10.1002/hec.4183. Epub 2020 Nov 3.

DOI:10.1002/hec.4183
PMID:33140488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8173671/
Abstract

This paper uses policy-induced variation in legal access to alcohol in the United States to explore interactions between genetic predispositions and health behaviors. It is well known that Minimum Legal Drinking Age (MLDA) laws have discrete impacts on binge drinking behaviors, but less is known about heterogeneity of the effects and the characteristics of individuals most and least affected. Using the Add Health data, this paper explores differential policy effects based on polygenic scores (PGS), which are genome-wide summary measures predicting health outcomes. Specifically, we leverage PGS for alcoholism and for a broader set of risk-taking behaviors to explore heterogeneities in response to the policy and consider mechanisms for the responses. Like previous literature using the Add Health and other datasets, we find main effects of MLDA in increasing recent binge drinking episodes by approximately 5 percentage points. We find MLDA effects are concentrated entirely in individuals with high PGS for alcohol use. We are also able to compare these results with measures of parental alcoholism as a global proxy for family history.

摘要

本文利用美国法律对酒精的获取的政策变化,来探索遗传倾向与健康行为之间的相互作用。众所周知,最低法定饮酒年龄(MLDA)法对狂饮行为有明显的影响,但对于这些影响的异质性以及受影响最大和最小的个体的特征,人们知之甚少。本文利用 Add Health 数据,基于多基因评分(PGS)来探索基于遗传因素的差异政策效应,PGS 是一种预测健康结果的全基因组综合测量方法。具体来说,我们利用酒精成瘾和更广泛的风险行为的 PGS,来探索对政策的反应的异质性,并考虑反应的机制。与之前使用 Add Health 和其他数据集的文献一样,我们发现 MLDA 的主要影响是使最近的狂饮事件增加了大约 5 个百分点。我们发现 MLDA 的影响完全集中在酒精使用 PGS 较高的个体中。我们还能够将这些结果与父母酗酒的指标进行比较,将其作为家族史的一个整体代理。

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本文引用的文献

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Genetic Endowments and Wealth Inequality.遗传天赋与财富不平等。
J Polit Econ. 2020 Apr;128(4):1474-1522. doi: 10.1086/705415.
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Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.对超过 100 万人的风险容忍度和冒险行为进行全基因组关联分析,确定了数百个位点和共同的遗传影响。
Nat Genet. 2019 Feb;51(2):245-257. doi: 10.1038/s41588-018-0309-3. Epub 2019 Jan 14.
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The personal and clinical utility of polygenic risk scores.多基因风险评分的个体和临床效用。
Nat Rev Genet. 2018 Sep;19(9):581-590. doi: 10.1038/s41576-018-0018-x.
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Legal access to alcohol and criminality.合法饮酒与犯罪。
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Genes, Environments, and Sex Differences in Alcohol Research.酒精研究中的基因、环境与性别差异
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The Genetics of Success: How Single-Nucleotide Polymorphisms Associated With Educational Attainment Relate to Life-Course Development.成功的遗传学:与受教育程度相关的单核苷酸多态性如何与生命历程发展相关联。
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The Mechanisms of Alcohol Control.酒精控制的机制。
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Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.通过全基因组分析确定的与主观幸福感、抑郁症状和神经质相关的基因变异。
Nat Genet. 2016 Jun;48(6):624-33. doi: 10.1038/ng.3552. Epub 2016 Apr 18.
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The Minimum Legal Drinking Age and Crime.最低法定饮酒年龄与犯罪
Rev Econ Stat. 2015 May;97(2):521-524. doi: 10.1162/REST_a_00489.
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The heritability of alcohol use disorders: a meta-analysis of twin and adoption studies.酒精使用障碍的遗传度:双生子和收养研究的荟萃分析
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