Abstract
Background: Both obesity and smoking are common in schizophrenia patients taking clozapine, causing cardiovascular disease and premature deaths. Methods: Two hundred and thirty-seven patients with schizophrenia or related psychoses treated with clozapine completed the Liverpool University Neuroleptic Assessment Scale (LUNSERS) and a questionnaire including current height, weight, changes therein and smoking status. Aims: The aim of this study was to analyze weight and weight change in smoking and non-smoking patients taking clozapine. A possible interaction between obesity and smoking was explored. Results: No association was found between weight change and smoking status during clozapine treatment. There was no significant difference in body mass index (BMI) between non-smokers and smokers. In the analysis of covariance (ANCOVA) with BMI as the dependent variable, the best fitting model comprised age, sex, intensity of sedation, and reported amount of smoking as explanatory variables (ηp2= 0.116; P = 0.029; power = 0.750). None of the explanatory proportions of any single factor was significant. Conclusions: Estimated according to reported weight gain and BMI, no difference was found between smoking and non-smoking clozapine-treated patients. Number of cigarettes smoked explained BMI if age and sex were taken into account. This result is in line with the findings of some general population studies, where heavy smoking has been associated with a greater risk of obesity.
Acknowledgements
This study was funded by the Satakunta Hospital District Research Foundation (EVO-funding). Acknowledgements to Ms. Ulla Hohtari-Kivimäki MHS (Health Sci.) for valuable help with data collection and to Heini Huhtala Ph.D. for helping us design the statistical methods of the study.
Declaration of interest: N.S. has received support from Bristol-Myers Squibb and Janssen-Cilag for participating international congresses. E.L has received support from Otsuka for participating international congresses. M.V has consulted for AstraZeneca and Eli Lilly; conducted clinical trials for Bristol-Myers Squibb and received support from Bristol-Myers Squibb, Eli Lilly and Lundbeck for participating international congresses and received research grant from Lundbeck and Pfizer. O.K has consulted for Janssen-Cilag and Lundbeck.
The authors has not received any support from clozapine producers and are alone responsible for the content and writing of the paper.