Alcohol challenges in young men from alcoholic pedigrees and control families: A report from the COGA project

被引:111
作者
Schuckit, MA
Tsuang, JW
Anthenelli, RM
Tipp, JE
Nurnberger, JI
机构
[1] Department of Psychiatry (116A), Veterans Affairs Medical Center, University of California, San Diego, San Diego, CA 92161-2002
[2] Department of Psychiatry, W. Los Angeles Vet. Aff. Med. Center, Los Angeles, CA
[3] Department of Psychiatry, University of California, School of Medicine, San Diego, CA
[4] Department of Psychiatry, Indiana University Medical Center, Bloomington, IN
来源
JOURNAL OF STUDIES ON ALCOHOL | 1996年 / 57卷 / 04期
关键词
D O I
10.15288/jsa.1996.57.368
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
Objective: Alcoholism is a complex disorder that demonstrates genetic heterogeneity. Genetic linkage studied of alcohol dependence also suffer from the probability that many individuals who inherit an enhanced risk never develop the clinical syndrome. Thus, studies of genetic influences in alcohol abuse or dependence would benefit from the identification of characteristics of an individual that are associated with the probability of developing the disorder. A reduced responsivity to alcohol has been reported to characterize almost 40% of sons of alcoholics and to predict future alcohol abuse or dependence a decade later. This study explores the existence of this characteristic in a more heterogeneous sample that is part of a genetic pedigree study of families of alcoholics. Method: Eighteen to 30 year old subjects who were sons of alcohol dependent fathers and who were drinkers but not alcohol dependent were selected from pedigrees of alcoholics at all six sites of the Collaborative Study on the Genetics of Alcoholism (COGA) study. Family history negative controls matched on demography and substance use histories were selected for each subject. Data were obtained on 20 pairs of high-risk and low-risk men (40 subjects) following a challenge with 0.72 g/kg (0.9 ml/kg) of ethanol. Evaluations included measures of subjective feelings of intoxication and body sway, and changes in cortisol, ACTH and prolactin. Results: The data corroborate a lower level of intensity of response of alcohol in the sons of alcoholics especially as measured by changes in cortisol, with similar but less robust changes in subjective feelings and other measures. Conclusions: The results expand upon earlier studies by using a more heterogeneous population of men at high alcoholism risk. The data highlight the possible usefulness of the reduced response to alcohol as an adjunct to future linkage analyses.
引用
收藏
页码:368 / 377
页数:10
相关论文
共 30 条
[1]  
[Anonymous], 1987, DIAGNOSTIC STAT MANU, V4th
[2]   EEG, AUTONOMIC AND SUBJECTIVE CORRELATES OF THE RISK FOR ALCOHOLISM [J].
BAUER, LO ;
HESSELBROCK, VM .
JOURNAL OF STUDIES ON ALCOHOL, 1993, 54 (05) :577-589
[3]   A NEW, SEMISTRUCTURED PSYCHIATRIC INTERVIEW FOR USE IN GENETIC-LINKAGE STUDIES - A REPORT ON THE RELIABILITY OF THE SSAGA [J].
BUCHOLZ, KK ;
CADORET, R ;
CLONINGER, CR ;
DINWIDDIE, SH ;
HESSELBROCK, VM ;
NURNBERGER, JI ;
REICH, T ;
SCHMIDT, I ;
SCHUCKIT, MA .
JOURNAL OF STUDIES ON ALCOHOL, 1994, 55 (02) :149-158
[4]  
CHAKRAVARTI A, 1990, BANB REPORT, V33, P307
[5]   GENETICS OF ALCOHOLISM [J].
DEVOR, EJ ;
CLONINGER, CR .
ANNUAL REVIEW OF GENETICS, 1989, 23 :19-36
[6]   DIAGNOSTIC CRITERIA FOR USE IN PSYCHIATRIC RESEARCH [J].
FEIGHNER, JP ;
WOODRUFF, RA ;
WINOKUR, G ;
MUNOZ, R ;
ROBINS, E ;
GUZE, SB .
ARCHIVES OF GENERAL PSYCHIATRY, 1972, 26 (01) :57-&
[7]  
HEALTH AC, 1992, J STUD ALCOHOL, V53, P262
[8]  
IRWIN M, 1988, AM J PSYCHIAT, V145, P595
[9]  
KEPPEL GK, 1991, DESIGN ANAL RES HDB, P383
[10]   SELECTIVE BREEDING FOR ALCOHOL PREFERENCE AND ASSOCIATED RESPONSES [J].
LI, TK ;
LUMENG, L ;
DOOLITTLE, DP .
BEHAVIOR GENETICS, 1993, 23 (02) :163-170