4.2 Article

A Longitudinal Twin Study of Effects of Adolescent Alcohol Abuse on the Neurophysiology of Attention and Orienting

期刊

ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH
卷 35, 期 7, 页码 1339-1350

出版社

WILEY-BLACKWELL
DOI: 10.1111/j.1530-0277.2011.01470.x

关键词

Adolescents; Alcohol Abuse; Event-Related Potentials; P3; Twin Study

资金

  1. National Institute on Alcohol Abuse and Alcoholism [R37AA012502, R01AA08315]
  2. Academy of Finland (Center of Excellence in Complex Disease Genetics) [1211486, 118555, 100499]
  3. Emil Aaltonen Foundation
  4. Finnish Cultural Foundation
  5. Jenny and Antti Wihuri Foundation
  6. Finnish Foundation for Alcohol Studies
  7. Ella and Georg Ehrnrooth Foundation
  8. Yrjo Jahnsson Foundation
  9. NIH [R01MH083744, R01HD040712, R01NS037462, R01NS048279]

向作者/读者索取更多资源

Background: Long-term functional brain effects of adolescent alcohol abuse remain uncertain, partially because of difficulties in distinguishing inherited deficits from neuronal effects of ethanol and by confounds associated with alcohol abuse, especially nicotine exposure. We conducted a longitudinal twin study to determine neurocognitive effects of adolescent alcohol abuse, as measured with the auditory event-related potential (ERP) component P3, a putative marker of genetic vulnerability to alcoholism. Methods: Twin pairs (N = 177; 150 selected for intrapair concordance/discordance for alcohol-related problems at age 18 1/2) were recruited from ongoing studies of twins born 1975-1979 in Finland. Alcohol and tobacco use were assessed with questionnaires at ages 16, 17, 18 1/2, and similar to 25, and by a structured psychiatric interview concurrent with the ERP testing at mean age 25.8. During ERP recordings, subjects were instructed to detect target tones within a train of frequent standards and to ignore occasional novel sounds. To distinguish familial factors from ethanol effects, ERP and self-reported alcohol use measures were incorporated into hierarchical multiple regression (HMR) analysis, and intrapair differences in ERP were associated with intrapair differences in alcohol variables. Results: Novel-sound P3 amplitude correlated negatively with self-reported alcohol use in both between- and within-family analyses. No similar effect was observed for target-tone P3. HMR results suggest that twins' similarity for novel-sound P3 amplitude is modulated by their alcohol use, and this effect of alcohol use is influenced by genetic factors. Conclusions: Our results, from a large sample of twins selected from a population-based registry for pairwise concordance/discordance for alcohol problems at 18 1/2, demonstrate that adolescent alcohol abuse is associated with subtle neurophysiological changes in attention and orienting. The changes are reflected in decreased novel-sound P3 amplitude and may be modified by genetic factors.

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