Glucose intolerance with atypical antipsychotics

被引:84
作者
Hedenmalm, K
Hägg, S
Ståhl, M
Mortimer, Ö
Spigset, O
机构
[1] Med Prod Agcy, Drug Epidemiol Unit, S-75103 Uppsala, Sweden
[2] Norrland Univ Hosp, Div Clin Pharmacol, Umea, Sweden
[3] WHO Uppsala Monitoring Ctr, Uppsala, Sweden
[4] St Olavs Univ Hosp, Dept Clin Pharmacol, Trondheim, Norway
关键词
D O I
10.2165/00002018-200225150-00005
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Previous studies have suggested that the atypical antipsychotics clozapine and olanzapine may be associated with an increased risk of glucose intolerance and diabetes mellitus. Early studies have also suggested an association between use of conventional antipsychotics and the development of glucose intolerance. Objective: To examine quantitatively the association between glucose intolerance including diabetes mellitus and the use of the atypical antipsychotics clozapine, olanzapine or risperidone, and to identify possible risk factors for the development of glucose intolerance during treatment with these drugs. Methods: All reports suggestive of glucose intolerance for clozapine, olanzapine and risperidone were identified in the WHO database for adverse drug reactions. In the analyses of possible risk factors for glucose intolerance all other reports of adverse drug reactions for clozapine, olanzapine and risperidone were used as reference. Using the Bayesian Confidence Propagation Neural Network method, the strengths of the associations over time between glucose intolerance and the use of these drugs were analysed. For comparison, the strengths of the associations between glucose intolerance and the use of the conventional antipsychotics haloperidol and chlorpromazine were also analysed. Results: Clozapine, olanzapine and risperidone were significantly associated with glucose intolerance. In contrast, chlorpromazine and haloperidol were not associated with glucose intolerance. For clozapine, olanzapine and risperidone grouped together, the following potential risk factors for glucose intolerance were identified: an underlying diabetic condition (odds ratio [OR] 10.22,95% CI 8.20-12.73), an increase in weight (OR 2.36, 95% Cl 1.76-3.17), male gender (OR 1.27, 95% Cl 1.11-1.47), and concomitant use of valproic acid (OR 1.97, 95% Cl 1.61-2.40), selective serotonin reuptake inhibitors (OR 1.63, 95% Cl 1.33-1.99) or buspirone (OR 2.24, 95% Cl 1.33-3.77). Conclusion: Treatment with clozapine, olanzapine or risperidone appears to be associated with an increased risk of glucose intolerance.
引用
收藏
页码:1107 / 1116
页数:10
相关论文
共 39 条
[1]  
Allison DB, 1999, AM J PSYCHIAT, V156, P1686
[2]  
ARNESON GA, 1964, J NEUROPSYCHIATRY, V5, P181
[3]   A Bayesian neural network method for adverse drug reaction signal generation [J].
Bate, A ;
Lindquist, M ;
Edwards, IR ;
Olsson, S ;
Orre, R ;
Lansner, A ;
De Freitas, RM .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1998, 54 (04) :315-321
[4]   Olanzapine-induced glucose dysregulation [J].
Bettinger, TL ;
Mendelson, SC ;
Dorson, PG ;
Crismon, ML .
ANNALS OF PHARMACOTHERAPY, 2000, 34 (7-8) :865-867
[5]  
BRAMBILLA F, 1976, DIS NERV SYST, V37, P98
[6]   Serum leptin levels increase rapidly after initiation of clozapine therapy [J].
Bromel, T ;
Blum, WF ;
Ziegler, A ;
Schulz, E ;
Bender, M ;
Fleischhaker, C ;
Remschmidt, H ;
Krieg, JC ;
Hebebrand, J .
MOLECULAR PSYCHIATRY, 1998, 3 (01) :76-80
[7]  
DYNES JB, 1969, DIS NERV SYST, V30, P341
[8]   Concepts in risk-benefit assessment - A simple merit analysis of a medicine? [J].
Edwards, IR ;
Wiholm, BE ;
Martinez, C .
DRUG SAFETY, 1996, 15 (01) :1-7
[9]   Effect of some antidepressants on glycaemia and insulin levels of normoglycaemic and alloxan-induced hyperglycaemic mice [J].
Erenmemisoglu, A ;
Ozdogan, UK ;
Saraymen, R ;
Tutus, A .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1999, 51 (06) :741-743
[10]  
Gaulin BD, 1999, AM J PSYCHIAT, V156, P1270