Effects of ondansetron in early-versus late-onset alcoholics: A prospective, open-label study

被引:87
作者
Kranzler, HR [1 ]
Pierucci-Lagha, A [1 ]
Feinn, R [1 ]
Hernandez-Avila, C [1 ]
机构
[1] Univ Connecticut, Sch Med, Dept Psychiat, Alcohol Res Ctr, Farmington, CT 06030 USA
来源
ALCOHOL-CLINICAL AND EXPERIMENTAL RESEARCH | 2003年 / 27卷 / 07期
关键词
ondansetron; 5-HT3; antagonist; alcoholism subtype; serotonin function; alcoholism treatment;
D O I
10.1097/01.ALC.0000075547.77464.76
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: Early-onset alcoholics (EOAs) have a greater familial loading for alcoholism, more severe progression of the disorder, a greater severity of comorbild. psychopathology, and a poorer response to treatment than late-onset alcoholics (LOAs). Ondansetron, a 5-hydroxytryptamine-3-antagonist, was found to be superior to placebo in the treatment of EOAs, but not of LOAs. This study compared the tolerability, and potential efficacy of an oral solution of ondansetron in EOAs versus LOAs. Methods: Forty outpatients with alcohol dependence (67.5% male; 87.5% European American; 20 EOAs; 20 LOAs) received an oral solution of ondansetron at a dosage of 4 mug/kg twice daily for 8 weeks, together with weekly relapse-prevention therapy. Results: EOAs had a significantly greater decrease in drinks per day, drinks per drinking day, and alcohol-related problems than LOAs. Changes in the level, of carbohydrate-deficient transferrin were consistent with changes in self-reported drinking behavior. Conclusions: An oral solution of ondansetron seems suitable for the treatment of alcohol dependence, yielding findings consistent with evidence from a placebo-controlled trial that ondansetron, at a dosage of 4 mug/kg twice daily, is of value in the treatment of EOAs.
引用
收藏
页码:1150 / 1155
页数:6
相关论文
共 36 条
[1]  
Arndt T, 2001, CLIN CHEM, V47, P13
[2]  
BABOR TF, 1992, ARCH GEN PSYCHIAT, V49, P599
[3]   AN INVENTORY FOR MEASURING DEPRESSION [J].
BECK, AT ;
ERBAUGH, J ;
WARD, CH ;
MOCK, J ;
MENDELSOHN, M .
ARCHIVES OF GENERAL PSYCHIATRY, 1961, 4 (06) :561-&
[4]   DEVELOPMENT AND INITIAL VALIDATION OF A MEASURE OF DRINKING URGES IN ABSTINENT ALCOHOLICS [J].
BOHN, MJ ;
KRAHN, DD ;
STAEHLER, BA .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1995, 19 (03) :600-606
[5]   NEUROGENETIC ADAPTIVE-MECHANISMS IN ALCOHOLISM [J].
CLONINGER, CR .
SCIENCE, 1987, 236 (4800) :410-416
[6]  
CLONINGER CR, 1981, ARCH GEN PSYCHIAT, V38, P861
[7]  
DICHIARA G, 1988, P NATL ACAD SCI USA, V85, P5274
[8]  
Donovan, 1992, NIAAA PROJECT MATCH, V3
[9]   EFFECTS OF ONDANSETRON PRETREATMENT ON ACUTE RESPONSES TO ETHANOL IN SOCIAL DRINKERS [J].
DOTY, P ;
ZACNY, JP ;
DEWIT, H .
BEHAVIOURAL PHARMACOLOGY, 1994, 5 (4-5) :461-469
[10]   EVIDENCE THAT THE AMYGDALA IS INVOLVED IN THE INHIBITORY EFFECTS OF 5-HT3 RECEPTOR ANTAGONISTS ON ALCOHOL-DRINKING IN RATS [J].
DYR, W ;
KOSTOWSKI, W .
ALCOHOL, 1995, 12 (04) :387-391