Weight and metabolic changes in early psychosis-association with daily quantification of medication exposure during the first hospitalization.


Journal

Acta psychiatrica Scandinavica
ISSN: 1600-0447
Titre abrégé: Acta Psychiatr Scand
Pays: United States
ID NLM: 0370364

Informations de publication

Date de publication:
09 2023
Historique:
revised: 30 05 2023
received: 18 02 2023
accepted: 06 07 2023
medline: 23 8 2023
pubmed: 2 8 2023
entrez: 2 8 2023
Statut: ppublish

Résumé

The most common causes of death in schizophrenia are cardiovascular disorders, which are closely related to metabolic syndrome/obesity. To better understand the development of metabolic alterations early in the course of illness, we quantified daily medication exposure in the first days of the first hospitalization for psychosis and related it to changes in weight and metabolic markers. We recruited participants with first episode psychosis (FEP, N = 173) during their first psychiatric hospitalization and compared them to controls (N = 204). We prospectively collected weight, body mass index, metabolic markers, and exact daily medication exposure at admission and during hospitalization. Individuals with FEP gained on average 0.97 ± 2.26 BMI points or 3.46 ± 7.81 kg of weight after an average of 44.6 days of their first inpatient treatment. Greater antipsychotic exposure was associated with greater BMI increase, but only in people with normal/low baseline BMI. Additional predictors of weight gain included type of medication and duration of treatment. Medication exposure was not directly related to metabolic markers, but higher BMI was associated with higher TGC, TSH, and lower HDL. Following inpatient treatment, participants with FEP had significantly higher BMI, TGC, prolactin, and lower fT4, HDL than controls. During their first admission, people with FEP, especially those with normal/low baseline BMI, showed a rapid and clinically significant weight increase, which was associated with exposure to antipsychotics, and with metabolic changes consistent with metabolic syndrome. These findings emphasize weight monitoring in FEP and suggest a greater need for caution when prescribing metabolically problematic antipsychotics to people with lower BMI.

Sections du résumé

BACKGROUND
The most common causes of death in schizophrenia are cardiovascular disorders, which are closely related to metabolic syndrome/obesity. To better understand the development of metabolic alterations early in the course of illness, we quantified daily medication exposure in the first days of the first hospitalization for psychosis and related it to changes in weight and metabolic markers.
STUDY DESIGN
We recruited participants with first episode psychosis (FEP, N = 173) during their first psychiatric hospitalization and compared them to controls (N = 204). We prospectively collected weight, body mass index, metabolic markers, and exact daily medication exposure at admission and during hospitalization.
STUDY RESULTS
Individuals with FEP gained on average 0.97 ± 2.26 BMI points or 3.46 ± 7.81 kg of weight after an average of 44.6 days of their first inpatient treatment. Greater antipsychotic exposure was associated with greater BMI increase, but only in people with normal/low baseline BMI. Additional predictors of weight gain included type of medication and duration of treatment. Medication exposure was not directly related to metabolic markers, but higher BMI was associated with higher TGC, TSH, and lower HDL. Following inpatient treatment, participants with FEP had significantly higher BMI, TGC, prolactin, and lower fT4, HDL than controls.
CONCLUSION
During their first admission, people with FEP, especially those with normal/low baseline BMI, showed a rapid and clinically significant weight increase, which was associated with exposure to antipsychotics, and with metabolic changes consistent with metabolic syndrome. These findings emphasize weight monitoring in FEP and suggest a greater need for caution when prescribing metabolically problematic antipsychotics to people with lower BMI.

Identifiants

pubmed: 37528692
doi: 10.1111/acps.13594
doi:

Substances chimiques

Antipsychotic Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

265-276

Subventions

Organisme : CIHR
ID : 180449
Pays : Canada
Organisme : CIHR
ID : 142255
Pays : Canada

Informations de copyright

© 2023 The Authors. Acta Psychiatrica Scandinavica published by John Wiley & Sons Ltd.

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Auteurs

Kristyna Vochoskova (K)

National Institute of Mental Health, Klecany, Czech Republic.
Third Faculty of Medicine, Charles University, Prague, Czech Republic.

Sean R McWhinney (SR)

Department of Psychiatry, Dalhousie University, Halifax, Canada.

Marketa Fialova (M)

National Institute of Mental Health, Klecany, Czech Republic.
Third Faculty of Medicine, Charles University, Prague, Czech Republic.

Marian Kolenic (M)

National Institute of Mental Health, Klecany, Czech Republic.
Third Faculty of Medicine, Charles University, Prague, Czech Republic.

Filip Spaniel (F)

National Institute of Mental Health, Klecany, Czech Republic.
Third Faculty of Medicine, Charles University, Prague, Czech Republic.

Patrik Svancer (P)

National Institute of Mental Health, Klecany, Czech Republic.
Third Faculty of Medicine, Charles University, Prague, Czech Republic.

Petra Boron (P)

Psychiatric Hospital Bohnice, Prague, Czech Republic.

Yurai Okaji (Y)

Psychiatric Hospital Bohnice, Prague, Czech Republic.

Pavel Trancik (P)

Psychiatric Hospital Bohnice, Prague, Czech Republic.

Tomas Hajek (T)

National Institute of Mental Health, Klecany, Czech Republic.
Third Faculty of Medicine, Charles University, Prague, Czech Republic.
Department of Psychiatry, Dalhousie University, Halifax, Canada.

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