Association of alcohol dehydrogenase genes with alcohol dependence: a comprehensive analysis

被引:179
作者
Edenberg, HJ [1 ]
Xuei, XL
Chen, HJ
Tian, HJ
Wetherill, LF
Dick, DM
Almasy, L
Bierut, L
Bucholz, KK
Goate, A
Hesselbrock, V
Kuperman, S
Nurnberger, J
Porjesz, B
Rice, J
Schuckit, M
Tischfield, J
Begleiter, H
Foroud, T
机构
[1] Indiana Univ, Sch Med, Indianapolis, IN 46202 USA
[2] Washington Univ, Sch Med, St Louis, MO USA
[3] SW Fdn Biomed Res, San Antonio, TX 78284 USA
[4] Univ Connecticut, Farmington, CT USA
[5] Univ Iowa, Carver Coll Med, Iowa City, IA USA
[6] SUNY Hlth Sci Ctr, Brooklyn, NY 11203 USA
[7] Univ Calif San Diego, San Diego, CA 92103 USA
[8] Rutgers State Univ, Piscataway, NJ USA
基金
美国国家卫生研究院;
关键词
D O I
10.1093/hmg/ddl073
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Linkage evidence indicated that gene(s) located on chromosome 4q, in the region of the alcohol dehydrogenase (ADH) genes, affected risk for alcoholism. We genotyped 110 single nucleotide polymorphisms (SNPs) across the seven ADH genes and analyzed their association with alcoholism in a set of families with multiple alcoholic members, using the pedigree disequilibrium test. There was strong evidence that variations in ADH4 are associated with alcoholism: 12 SNPs were significantly associated. The region of strongest association ran from intron 1 to 19.5 kb beyond the 3' end of the gene. Haplotype tag SNPs were selected for the block in the ADH4 gene that provided evidence of association and subsequently used in association analysis; the haplotype was significantly associated with alcoholism (P=0.01) There was weaker evidence that variations in ADH1A and ADH1B might also play a role in modifying risk. Among African-Americans, there was evidence that the ADH1B*3 allele was protective.
引用
收藏
页码:1539 / 1549
页数:11
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