AI Article Synopsis

  • A nationwide study in Korea investigated how common metabolic syndrome (MetS) is among patients with schizophrenia or schizoaffective disorder and its link to antipsychotic medications.
  • The study included 845 patients aged 18-65 from 16 hospitals, finding that MetS affected 36.5% of the participants, with a higher prevalence in men compared to women.
  • The study highlights the need for regular screening for MetS in patients on antipsychotics due to the high rates associated with different types of these medications.

Article Abstract

Objective: We designed a nationwide study with limited exclusion criteria to investigate the prevalence of metabolic syndrome (MetS) in Korea and its relationship with antipsychotic medications.

Methods: This multicenter, cross-sectional, and observational study included patients diagnosed with schizophrenia or schizoaffective disorder. Sixteen hospitals enrolled 845 patients aged 18 to 65 years prescribed any antipsychotic medication between August 2011 and August 2013. MetS was diagnosed using the criteria of the modified Adult Treatment Panel III of the National Cholesterol Education Program with the Korean abdominal obesity definition (waist circumference ≥85 cm in women, ≥90 cm in men).

Results: The prevalence of MetS in all patients was 36.5% and was significantly higher in men than women (men, 40.8%; women, 32.2%) and was significantly correlated with age [odds ratio (OR) 1.02] and duration of illness (OR 1.03). The prevalence of MetS across antipsychotic drugs in the major monotherapy group was as follows: 18.8% for quetiapine, 22.0% for aripiprazole, 33.3% for both amisulpride and paliperidone, 34.0% for olanzapine, 35% for risperidone, 39.4% for haloperidol, and 44.7% for clozapine.

Conclusion: The prevalence of MetS is very high in patients with schizophrenia or schizoaffective disorder. Screening and monitoring of MetS is also strongly recommended.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240463PMC
http://dx.doi.org/10.4306/pi.2017.14.1.44DOI Listing

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