Undiagnosed metabolic syndrome and other adverse effects among clozapine users of Xhosa descent

dc.contributor.authorFaasen, N.en_ZA
dc.contributor.authorNiehaus, Dana J. H.en_ZA
dc.contributor.authorKoen, L.en_ZA
dc.contributor.authorJordaan, E.en_ZA
dc.date.accessioned2016-07-06T06:38:38Z
dc.date.available2016-07-06T06:38:38Z
dc.date.issued2014-07
dc.descriptionCITATION: Faasen, N., Niehaus, D.J. ., Koen, L. & Jordaan, E. 2014. Undiagnosed metabolic syndrome and other adverse effects among clozapine users of Xhosa descent. South African Journal of Psychiatry, 20(2):54-57, doi:10.7196/SAJP.528.en_ZA
dc.descriptionThe original publication is available at http://www.sajp.org.zaen_ZA
dc.description.abstractBackground. Clozapine use is known to be associated with significant side-effects, including prolongation of the QT-interval, agranulocytosis and metabolic syndrome. However, few data exist on the prevalence of clozapine side-effects in patients of Xhosa descent. Objective. To gather data from Xhosa patients with schizophrenia to establish the prevalence of clozapine side-effects in this population. Methods. Twenty-nine Xhosa patients with schizophrenia (as per the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR)) who had been receiving clozapine treatment for >1 year on an outpatient basis were selected for inclusion. All patients were participating in a genetics study in the Cape Metropolitan area. The participants were evaluated for the presence of side-effects (tests including an electrocardiogram, white blood cell count (WCC) and fasting blood glucose). Results. The prevalence of metabolic syndrome was 44.8% (95% confidence interval (CI) 26.7 - 62.9) and of undiagnosed diabetes mellitus 13.8% (95% CI 1.24 - 26.34). There was a significant association between metabolic syndrome and body mass index (BMI) (p<0.01). The mean (SD) WCC was 7.8 × 109/L (2.8), with 3.4% of the subjects having a WCC <3.5 × 109/L. Sedation (82.8%; 95% CI 69.0 - 96.5), hypersalivation (79.3%; 95% CI 64.6 - 94.1) and constipation (44.8%; 95% CI 26.7 - 62.9) were common. The mean QT-interval was 373.8 (35.9) ms and 10% had a corrected QT-interval >440 ms. There was an association between the duration of clozapine treatment and QT-interval (with Bazett’s correction). Conclusion. The high prevalence of metabolic syndrome and undiagnosed diabetes mellitus in this sample points to a need to monitor glucose levels and BMI on a regular basis. A larger study should be done to accurately quantify the differences in prevalence of side-effects between population groups.en_ZA
dc.description.urihttp://www.sajp.org.za/index.php/sajp/article/view/528
dc.description.versionPublisher's versionen_ZA
dc.format.extent4 pages
dc.identifier.citationFaasen, N., Niehaus, D.J.H., Koen, L. & Jordaan, E. 2014. Undiagnosed metabolic syndrome and other adverse effects among clozapine users of Xhosa descent. South African Journal of Psychiatry, 20(2):54-57, doi:10.7196/SAJP.528.en_ZA
dc.identifier.issn2078-6786 (online)
dc.identifier.issn1608-9685 (print)
dc.identifier.otherdoi:10.7196/SAJP.528
dc.identifier.urihttp://hdl.handle.net/10019.1/99085
dc.language.isoen_ZAen_ZA
dc.publisherAOSIS Publishingen_ZA
dc.rights.holderAuthors retain copyrighten_ZA
dc.subjectSchizophrenia --Treatment -- Complicationsen_ZA
dc.subjectMetabolic syndromeen_ZA
dc.subjectClozapine -- Side effectsen_ZA
dc.subjectXhosa (African people)en_ZA
dc.titleUndiagnosed metabolic syndrome and other adverse effects among clozapine users of Xhosa descenten_ZA
dc.typeArticleen_ZA
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