The level of response to alcohol in daughters of alcoholics and controls

被引:91
作者
Eng, MY
Schuckit, MA
Smith, TL
机构
[1] Univ Calif San Diego, Dept Psychiat 116A, Vet Affairs San Diego Healthcare Syst, San Diego, CA 92161 USA
[2] Univ Calif San Diego, San Diego State Univ, San Diego Joint Doctoral Program Clin Psychol, San Diego, CA 92120 USA
关键词
level of response; daughters of alcoholics; alcohol use disorders;
D O I
10.1016/j.drugalcdep.2005.01.002
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: The low level of response (LR) to alcohol is a genetically influenced characteristic related to the development of alcohol use disorders (AUDs). This phenotype is found in men with a family history (FH) of alcoholism, predicts future AUDs, and has heritabilities as high as 60%. However, despite evidence of genetic influences for AUDs in both sexes, the majority of studies evaluating differences in LR across high- and low-risk groups have been conducted on males, and it is unclear how generalizable these results are to women. Methods: Twenty-five women who are family history positive (FHP) for alcohol dependence were matched with 25 women with no FH of alcoholism (FHN) on factors that may impact LR. Using an alcohol challenge paradigm, data on the reaction to a moderate dose of alcohol were gathered over a period of 3.5 h. Assessments included breath alcohol concentrations (BrACs), the Subjective High Assessment Scale (SHAS), as well as body sway or static ataxia. Results: Family history positives reported lower subjective intoxication than FHNs. In addition, when body sway scores were corrected for skewness, FHPs had significantly lower scores on alcohol-related changes in lateral sway. These differences remained after considering the effects of drinking history and BrAC values. Conclusions: This study evaluated the LR to alcohol in the largest sample of alcohol challenges in matched FHP and FHN women to date. Overall, the findings are consistent with most data from earlier investigations of smaller sized samples of FHP women. The results suggest that, similar to sons of alcoholics, a low LR to alcohol might also be characteristic of daughters of alcoholics. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:83 / 93
页数:11
相关论文
共 90 条
[1]  
[Anonymous], 1987, DIAGNOSTIC STAT MANU, V4th
[2]   DIFFERENTIAL-EFFECTS OF ETHANOL ON PUNISHED RESPONDING IN THE P-RATS AND NP-RATS [J].
BALDWIN, HA ;
WALL, TL ;
SCHUCKIT, MA ;
KOOB, GF .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1991, 15 (04) :700-704
[3]   The relationship between the family density of alcoholism and externalizing symptoms among 146 children [J].
Barnow, S ;
Schuckit, M ;
Smith, TL ;
Preuss, U ;
Danko, G .
ALCOHOL AND ALCOHOLISM, 2002, 37 (04) :383-387
[4]   Rearing condition and rh5-HTTLPR interact to influence limbic-hypothalamic-pituitary-adrenal axis response to stress in infant macaques [J].
Barr, CS ;
Newman, TK ;
Shannon, C ;
Parker, C ;
Dvoskin, RL ;
Becker, ML ;
Schwandt, M ;
Champoux, M ;
Lesch, KP ;
Goldman, D ;
Suomi, SJ ;
Higley, JD .
BIOLOGICAL PSYCHIATRY, 2004, 55 (07) :733-738
[5]   RELIABILITY OF INDIVIDUAL DIAGNOSTIC CRITERION ITEMS FOR PSYCHOACTIVE SUBSTANCE DEPENDENCE AND THE IMPACT ON DIAGNOSIS [J].
BUCHOLZ, KK ;
HESSELBROCK, VM ;
SHAYKA, JJ ;
NURNBERGER, JI ;
SCHUCKIT, MA ;
SCHMIDT, I ;
REICH, T .
JOURNAL OF STUDIES ON ALCOHOL, 1995, 56 (05) :500-505
[6]   COMPARISON OF ALCOHOL DEPENDENCE IN SUBJECTS FROM CLINICAL, COMMUNITY, AND FAMILY STUDIES [J].
BUCHOLZ, KK ;
HELZER, JE ;
SHAYKA, JJ ;
LEWIS, CE .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1994, 18 (05) :1091-1099
[7]   Interaction between the functional polymorphisms of the alcohol-metabolism genes in protection against alcoholism [J].
Chen, CC ;
Lu, RB ;
Chen, YC ;
Wang, MF ;
Chang, YC ;
Li, TK ;
Yin, SJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (03) :795-807
[8]   Effects of the menstrual cycle of white women on ethanol toxicokinetics [J].
Corrêa, CL ;
Oga, S .
JOURNAL OF STUDIES ON ALCOHOL, 2004, 65 (02) :227-231
[9]   Elevated alcohol consumption in null mutant mice lacking 5-HT1B serotonin receptors [J].
Crabbe, JC ;
Phillips, TJ ;
Feller, DJ ;
Hen, R ;
Wenger, CD ;
Lessov, CN ;
Schafer, GL .
NATURE GENETICS, 1996, 14 (01) :98-101
[10]  
DEWIT H, 1990, ALCOHOL CLIN EXP RES, V14, P63