Olanzapine, weight change and metabolic effects: a naturalistic 12-month follow up

Objective: Olanzapine is an atypical antipsychotic drug used to treat schizophrenia. Some of the adverse effects related to its use are obesity, hyperlipidemia, type 2 diabetes and hypertension, which may result in development of metabolic syndrome. This study aimed to investigate a possible increas...

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Veröffentlicht in:Therapeutic advances in psychopharmacology 2014-02, Vol.4 (1), p.30-36
Hauptverfasser: Salviato Balbão, Marina, Cecílio Hallak, Jaime Eduardo, Arcoverde Nunes, Emerson, Homem de Mello, Mauricio, Triffoni-Melo, Andresa de Toledo, Ferreira, Flavia Isaura de Santi, Chaves, Cristiano, Durão, Ana Maria Sertori, Ramos, Adriana Pelegrino Pinho, de Souza Crippa, José Alexandre, Queiroz, Regina Helena Costa
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container_end_page 36
container_issue 1
container_start_page 30
container_title Therapeutic advances in psychopharmacology
container_volume 4
creator Salviato Balbão, Marina
Cecílio Hallak, Jaime Eduardo
Arcoverde Nunes, Emerson
Homem de Mello, Mauricio
Triffoni-Melo, Andresa de Toledo
Ferreira, Flavia Isaura de Santi
Chaves, Cristiano
Durão, Ana Maria Sertori
Ramos, Adriana Pelegrino Pinho
de Souza Crippa, José Alexandre
Queiroz, Regina Helena Costa
description Objective: Olanzapine is an atypical antipsychotic drug used to treat schizophrenia. Some of the adverse effects related to its use are obesity, hyperlipidemia, type 2 diabetes and hypertension, which may result in development of metabolic syndrome. This study aimed to investigate a possible increase in some anthropometric and biochemical parameters, and the existence of any correlation between them in Brazilian patients with schizophrenia treated with olanzapine in the mid term. Methods: Thirty subjects with schizophrenia were evaluated, 16 women and 14 men, aged between 18 and 47 years. All patients underwent blood collection and anthropometric measurements at four different times during 12 months of follow up; thus each patient was his or her own control. Results: Evaluation of some anthropometric measurements showed significant differences when comparing the mean values obtained in each of the different data collection times (p < 0.05). However, the biochemical indicators of development of metabolic syndrome measured in our study did not show the same rate of increment, with only the total cholesterol and glucose levels presenting statistically significant changes (p < 0.05), but without the same magnitude of weight change. Conclusion: We conclude that medium-term treatment with olanzapine promoted a substantial weight gain and increased visceral fat, while the metabolic profile did not show the same magnitude of change, suggesting a dissociation between weight gain and blood parameters, despite the severe weight gain observed among subjects evaluated.
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Some of the adverse effects related to its use are obesity, hyperlipidemia, type 2 diabetes and hypertension, which may result in development of metabolic syndrome. This study aimed to investigate a possible increase in some anthropometric and biochemical parameters, and the existence of any correlation between them in Brazilian patients with schizophrenia treated with olanzapine in the mid term. Methods: Thirty subjects with schizophrenia were evaluated, 16 women and 14 men, aged between 18 and 47 years. All patients underwent blood collection and anthropometric measurements at four different times during 12 months of follow up; thus each patient was his or her own control. Results: Evaluation of some anthropometric measurements showed significant differences when comparing the mean values obtained in each of the different data collection times (p &lt; 0.05). However, the biochemical indicators of development of metabolic syndrome measured in our study did not show the same rate of increment, with only the total cholesterol and glucose levels presenting statistically significant changes (p &lt; 0.05), but without the same magnitude of weight change. 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title Olanzapine, weight change and metabolic effects: a naturalistic 12-month follow up
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