Genetics of event-related brain potentials in response to a semantic priming paradigm in families with a history of alcoholism

被引:43
作者
Almasy, L
Porjesz, B
Blangero, J
Goate, A
Edenberg, HJ
Chorlian, DB
Kuperman, S
O'Connor, SJ
Rohrbaugh, J
Bauer, LO
Foroud, T
Rice, JP
Reich, T
Begleiter, H
机构
[1] SW Fdn Biomed Res, Dept Genet, San Antonio, TX 78245 USA
[2] SUNY Hlth Sci Ctr, Dept Psychiat, Brooklyn, NY 11203 USA
[3] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[4] Indiana Univ, Sch Med, Dept Biochem & Mol Biol, Indianapolis, IN USA
[5] Indiana Univ, Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46202 USA
[6] Univ Iowa, Dept Psychiat Res, Iowa City, IA USA
[7] Univ Connecticut, Ctr Hlth, Dept Psychiat, Farmington, CT 06032 USA
关键词
D O I
10.1086/316936
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Event-related brain potentials (ERPs) are altered in patients with a variety of psychiatric disorders and may represent quantitative correlates of disease liability that are more amenable to genetic analysis than disease status itself. Results of a genomewide linkage screen are presented for amplitude of the N4 and P3 components of the ERP, measured at 19 scalp locations in response to a semantic priming task for 604 individuals in 100 pedigrees ascertained as part of the Collaborative Study on the Genetics of Alcoholism. N4 and P3 amplitudes in response to three stimuli (nonwords, primed words [i.e., antonyms], and unprimed words) all showed significant heritabilities, the highest being .54. Both N4 and P3 showed significant genetic correlations across stimulus type at a given lead and across leads within a stimulus, indicating shared genetic influences among the traits. There were also substantial genetic correlations between the N4 and P3 amplitudes for a given lead, even across stimulus type. N4 amplitudes showed suggestive evidence of linkage in several chromosomal regions, and P3 amplitudes showed significant evidence of linkage to chromosome 5 and suggestive evidence of linkage to chromosome 4.
引用
收藏
页码:128 / 135
页数:8
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