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Trajectories of daily antipsychotic use and weight gain in people hospitalized for the first episode of psychosis
K. Vochoskova, SR. McWhinney, M. Fialova, M. Kolenic, F. Spaniel, P. Furstova, P. Boron, Y. Okaji, P. Trancik, T. Hajek
Language English Country England, Great Britain
Document type Journal Article
Grant support
NV16-32791A
Ministerstvo Zdravotnictví Ceské Republiky
NLK
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PubMed Central
from 2020
ProQuest Central
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from 1991
- MeSH
- Antipsychotic Agents * therapeutic use adverse effects MeSH
- Adult MeSH
- Weight Gain * drug effects MeSH
- Hospitalization * statistics & numerical data MeSH
- Body Mass Index * MeSH
- Humans MeSH
- Young Adult MeSH
- Olanzapine therapeutic use MeSH
- Polypharmacy MeSH
- Prospective Studies MeSH
- Psychotic Disorders * drug therapy MeSH
- Risperidone therapeutic use adverse effects MeSH
- Risk Factors MeSH
- Schizophrenia * drug therapy MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
BACKGROUND: We need to better understand the risk factors and predictors of medication-related weight gain to improve metabolic health of individuals with schizophrenia. This study explores how trajectories of antipsychotic medication (AP) use impact body weight early in the course of schizophrenia. METHODS: We recruited 92 participants with first-episode psychosis (FEP, n = 92) during their first psychiatric hospitalization. We prospectively collected weight, body mass index (BMI), metabolic markers, and exact daily medication exposure during 6-week hospitalization. We quantified the trajectory of AP medication changes and AP polypharmacy using a novel approach based on meta-analytical ranking of medications and tested it as a predictor of weight gain together with traditional risk factors. RESULTS: Most people started treatment with risperidone (n = 57), followed by olanzapine (n = 29). Then, 48% of individuals remained on their first prescribed medication, while 33% of people remained on monotherapy. Almost half of the individuals (39/92) experienced escalation of medications, mostly switch to AP polypharmacy (90%). Only baseline BMI was a predictor of BMI change. Individuals in the top tercile of weight gain, compared to those in the bottom tercile, showed lower follow-up symptoms, a trend for longer prehospitalization antipsychotic treatment, and greater exposure to metabolically problematic medications. CONCLUSIONS: Early in the course of illness, during inpatient treatment, baseline BMI is the strongest and earliest predictor of weight gain on APs and is a better predictor than type of medication, polypharmacy, or medication switches. Baseline BMI predicted weight change over a period of weeks, when other traditional predictors demonstrated a much smaller effect.
3rd Faculty of Medicine Charles University Prague Czech Republic
Department of Psychiatry Dalhousie University Halifax NS Canada
References provided by Crossref.org
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