Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach

被引:68
作者
Wang, T
Franke, P
Neidt, H
Cichon, S
Knapp, M
Lichtermann, D
Maier, W
Propping, P
Nöthen, MM
机构
[1] Univ Bonn, Inst Human Genet, D-53111 Bonn, Germany
[2] Tongji Med Univ, Union Hosp, Dept Neurol, Wuhan 430022, Peoples R China
[3] Univ Bonn, Dept Psychiat, D-53105 Bonn, Germany
[4] Inst Med Biometry Informat & Epidemiol, D-53105 Bonn, Germany
关键词
COMT; substance abuse; addiction; behavior genetics; candidate gene;
D O I
10.1038/sj.mp.4000803
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
Catechol-O-methyltransferase (COMT) is a major component of the metabolic pathways of neurotransmitters such as dopamine, adrenaline, and noradrenaline. The activity of COMT is known to vary within the population; it exists in common high- and low-activity forms that are determined by a Val --> Met polymorphism at amino acid position 108/158 (in soluble or membrane-bound COMT). Recently, the low-activity allele was reported to contribute to the development of late-onset alcoholism in men.(1) The present study extends this study by utilizing a family-based association approach, and by including individuals with early-onset alcoholism. Although no significant transmission disequilibrium was found in the overall sample of 70 parent/offspring trios (TDT = 1.43, P = 0.23), we observed a preferential transmission of the low-activity allele to patients with an early onset of disease (n = 32, TDT = 4.83, P = 0.028). Our results provide further evidence for an involvement of the COMT low-activity allele in the development of alcoholism and demonstrate the need for further studies in large samples of alcoholic patients.
引用
收藏
页码:109 / 111
页数:3
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