A novel single nucleotide polymorphism of the neuropeptide Y (NPY) gene associated with alcohol dependence

被引:54
作者
Mottagui-Tabar, S
Prince, JA
Wahlestedt, C
Zhu, GS
Goldman, D
Heilig, M
机构
[1] NIAAA, NIH, Bethesda, MD 20892 USA
[2] Karolinska Inst, Ctr Genom & Bioinformat, Stockholm, Sweden
[3] NIAAA, Neurogenet Lab, NIH, Rockville, MD 20852 USA
[4] Scripps Res Inst, Jupiter, FL USA
关键词
neuropeptide Y polymorphisms; alcohol dependence; promoter; genetic association studies;
D O I
10.1097/01.ALC.0000164365.04961.B1
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Neuropepticle Y (NPY) is a major endogenous regulator of anxiety-related behaviors and emotionality. Transgenic work with NPY and null-mutant mice have implicated NPY in the control of alcohol consumption, suggesting that genetic variation of the prepro-NPY gene may also contribute to the heritability of alcoholism. The aim of this study was to examine whether polymorphic variants of the NPY gene are associated with the diagnosis of alcohol dependence. Methods: We compared allele frequencies of 5 NPY polymorphisms (-883-ins/del, -602, -399, -84, and + 1128) in a Nordic population of alcohol-dependent individuals (n = 428 mates; n = 149 females) and ethnically matched controls (n = 84 males; n = 93 females) for whom alcohol dependence or any diagnosis of substance disorder was excluded. Patients were further subtyped into type I (late-onset) and type 11 (early-onset) alcoholics. Results: The -602 marker showed a significant association with alcohol dependence (p = 0,0035; OR, 2.3; 95% Cl, 1.3-4.0); a trend level association was further observed for the -399 marker (p = 0.058; OR, 1.3; 95% CI, 0.99-1.7) and the + 1128 marker (p = 0.053; OR, 1.8; 95% CI, 0.99-3.1). The association for the -602 marker remained and was strengthened when analyzed in type I subjects only, although this association was not seen in type 11 patients, and there also was a significant association in the female subjects but not in males. The -602 single nucleotide polymorphism was in strong linkage dysequilibrium (r(2) = 0.7;p < 0.0001) with the + 1128 single nucleoticle polymorphism, which has previously been reported to be associated with a diagnosis of alcoholism. Haplotype-based association confirmed these results. Conclusions: We report a novel polymorphism at position -602 in the 5' region of the NPY gene that is significantly associated with alcohol dependence. We also describe the haplotype frequencies and linkage dysequilibrium pattern of four variations in that region.
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页码:702 / 707
页数:6
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