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酒精脱氢酶基因变异与美国原住民传教士印第安人酒精依赖的保护性关联。

Protective association of genetic variation in alcohol dehydrogenase with alcohol dependence in Native American Mission Indians.

作者信息

Wall Tamara L, Carr Lucinda G, Ehlers Cindy L

机构信息

Department of Neuropharmacology, Scripps Research Institute, San Diego, CA, USA.

出版信息

Am J Psychiatry. 2003 Jan;160(1):41-6. doi: 10.1176/appi.ajp.160.1.41.

Abstract

OBJECTIVE

Two alcohol dehydrogenase genes (ADH2 and ADH3 on chromosome 4) and one aldehyde dehydrogenase gene (ALDH2 on chromosome 12) exhibit functional polymorphisms. The goal of this study was to determine whether any associations exist between the ADH2, ADH3, and ALDH2 polymorphisms and alcohol dependence in a group of Native Americans. An additional goal was to determine if any associations exist between these polymorphisms and the endophenotype, maximum number of drinks ever consumed in a 24-hour period.

METHOD

Mission Indian adults (N=340) were recruited for participation from reservations in southern California. Each participant completed an interview with the Semi-Structured Assessment for the Genetics of Alcoholism. A blood sample was collected from each participant for genotyping at the ALDH2, ADH2, and ADH3 loci.

RESULTS

Sixty percent of all participants (72% of men and 53% of women) met lifetime DSM-III-R criteria for alcohol dependence. A significant difference in the ADH2 allele distributions was found between alcohol-dependent and non-alcohol-dependent participants. Those with alcohol dependence were significantly less likely to have the ADH23 allele (odds ratio=0.28) and significantly more likely to have the ADH21 allele (odds ratio=2.00) than those who were not alcohol dependent. Individuals with ADH2*3 reported a lower number of maximum drinks ever consumed in a 24-hour period, compared to those without this allele.

CONCLUSIONS

These results are consistent with genetic linkage studies showing protective associations for alcohol dependence and related behavior on chromosome 4 and suggest that ADH2 polymorphisms may account for these findings. These results also highlight the utility of evaluating protective factors in populations with high rates of alcohol dependence.

摘要

目的

两个酒精脱氢酶基因(位于4号染色体上的ADH2和ADH3)和一个乙醛脱氢酶基因(位于12号染色体上的ALDH2)呈现出功能多态性。本研究的目的是确定ADH2、ADH3和ALDH2多态性与一组美国原住民酒精依赖之间是否存在关联。另一个目的是确定这些多态性与内表型(24小时内饮用的最大饮酒量)之间是否存在关联。

方法

从南加州的保留地招募了使命印第安成年人(N = 340)参与研究。每位参与者完成了一份关于酒精中毒遗传学的半结构化评估访谈。从每位参与者采集血样,用于对ALDH2、ADH2和ADH3基因座进行基因分型。

结果

所有参与者中有60%(男性为72%,女性为53%)符合酒精依赖的终身DSM-III-R标准。在酒精依赖和非酒精依赖参与者之间发现ADH2等位基因分布存在显著差异。与非酒精依赖者相比,酒精依赖者携带ADH23等位基因的可能性显著更低(优势比 = 0.28),而携带ADH21等位基因的可能性显著更高(优势比 = 2.00)。与没有该等位基因的个体相比,携带ADH2*3的个体报告的24小时内饮用的最大饮酒量更低。

结论

这些结果与基因连锁研究一致,该研究表明4号染色体上存在与酒精依赖及相关行为的保护性关联,并表明ADH2多态性可能解释了这些发现。这些结果还突出了在酒精依赖率高的人群中评估保护因素的效用。

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