An acute psychosocial stressor increases drinking in non-treatment-seeking alcoholics

被引:55
|
作者
Thomas, Suzanne E. [1 ]
Bacon, Amy K. [1 ]
Randall, Patrick K. [1 ]
Brady, Kathleen T. [1 ]
See, Ronald E. [1 ]
机构
[1] Med Univ S Carolina, Inst Psychiat, Charleston Alcohol Res Ctr, Charleston, SC 29425 USA
关键词
Alcohol; Relapse; Cortisol; Stress; Gender; Model; SOCIAL STRESS; URGE QUESTIONNAIRE; CUE REACTIVITY; DSM-IV; RELAPSE; CONSUMPTION; VALIDATION; RESPONSES; BEHAVIOR; DISORDERS;
D O I
10.1007/s00213-010-2163-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although studies suggest that stress is an important reason for relapse in alcoholics, few controlled studies have been conducted to examine this assumption. Evidence of stress-potentiated drinking would substantiate this clinical observation and would contribute to the development of a model that would be valuable to alcohol treatment research. The hypothesis was tested that an acute psychosocial stressor, the Trier Social Stress Test (TSST), increases alcohol consumption in non-treatment-seeking alcoholics. Seventy-nine alcohol-dependent participants (40 women) were randomly assigned to receive the TSST or a no-stress condition. Immediately afterward, all participants received an initial dose of their preferred alcoholic beverage to achieve a target blood alcohol concentration of 0.03 g/dl (to prime subsequent drinking in the laboratory). Participants then participated in a mock taste test of two glasses of beer. Primary dependent measures were whether s/he drank all of the beer available (yes/no) and total amount of beer consumed (milliliters). Stressed participants were twice as likely as non-stressed participants to drink all of the beer available, a significant effect. Although the stressed group drank more milliliters than the non-stressed group, this effect failed to reach significance, likely due to ceiling effects. There were no significant stress group x gender effects on either outcome. This study supports that stress-potentiated drinking is valid and can be modeled in a clinical laboratory setting.
引用
收藏
页码:19 / 28
页数:10
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