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Long-Term Evolution of Metabolic Status in Patients with Schizophrenia Stably Maintained on Second-Generation Antipsychotics

OBJECTIVE: Second-generation antipsychotics (SGAs) increase the risk of metabolic syndrome (MetS). Despite the risk of MetS, SGAs may have to be continued with change in some patients. The aim of this study was to trace the evolution of MetS in these patients. METHODS: Patients with schizophrenia wh...

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Autores principales: Jeong, Seong Hoon, Lee, Nam Young, Kim, Se Hyun, Chung, In Won, Youn, Tak, Kang, Ung Gu, Ahn, Yong Min, You, Han Young, Kim, Yong Sik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neuropsychiatric Association 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018140/
https://www.ncbi.nlm.nih.gov/pubmed/29940717
http://dx.doi.org/10.30773/pi.2018.01.18.1
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author Jeong, Seong Hoon
Lee, Nam Young
Kim, Se Hyun
Chung, In Won
Youn, Tak
Kang, Ung Gu
Ahn, Yong Min
You, Han Young
Kim, Yong Sik
author_facet Jeong, Seong Hoon
Lee, Nam Young
Kim, Se Hyun
Chung, In Won
Youn, Tak
Kang, Ung Gu
Ahn, Yong Min
You, Han Young
Kim, Yong Sik
author_sort Jeong, Seong Hoon
collection PubMed
description OBJECTIVE: Second-generation antipsychotics (SGAs) increase the risk of metabolic syndrome (MetS). Despite the risk of MetS, SGAs may have to be continued with change in some patients. The aim of this study was to trace the evolution of MetS in these patients. METHODS: Patients with schizophrenia who had been maintained on a fixed SGA regimen for more than a year were followed-up without changing the regimen. Metabolic indicators were evaluated at baseline and at follow-up. Prevalence, incidence and spontaneous normalization rate of MetS were estimated. Risk factors that might have influenced the evolution were scrutinized. RESULTS: A total of 151 subjects were included. During the mean observation period of 389.9±162.4 days, the prevalence of MetS was increased from 35.1 to 45.0%. The incidence rate was 29.6%, while the normalization rate was 26.4%, risk factors affecting incidence were age (OR=1.09, 95% CI: 1.03–1.17), baseline continuous values of metabolic syndrome risk scores (cMetS, OR=1.77, 95% CI:1.29–2.55) and baseline body weight (OR=1.06, 95% CI: 1.01–1.13). Normalization was influenced by age (OR=0.74, 95% CI: 0.57–0.89) and baseline body weight (OR=0.85, 95% CI: 0.72–0.95). CONCLUSION: The prevalence of MetS steadily increased with the continuous use of SGAs. However, individual difference was extensive and about a quarter of the patients were able to recover naturally without specific measurements.
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spelling pubmed-60181402018-06-29 Long-Term Evolution of Metabolic Status in Patients with Schizophrenia Stably Maintained on Second-Generation Antipsychotics Jeong, Seong Hoon Lee, Nam Young Kim, Se Hyun Chung, In Won Youn, Tak Kang, Ung Gu Ahn, Yong Min You, Han Young Kim, Yong Sik Psychiatry Investig Original Article OBJECTIVE: Second-generation antipsychotics (SGAs) increase the risk of metabolic syndrome (MetS). Despite the risk of MetS, SGAs may have to be continued with change in some patients. The aim of this study was to trace the evolution of MetS in these patients. METHODS: Patients with schizophrenia who had been maintained on a fixed SGA regimen for more than a year were followed-up without changing the regimen. Metabolic indicators were evaluated at baseline and at follow-up. Prevalence, incidence and spontaneous normalization rate of MetS were estimated. Risk factors that might have influenced the evolution were scrutinized. RESULTS: A total of 151 subjects were included. During the mean observation period of 389.9±162.4 days, the prevalence of MetS was increased from 35.1 to 45.0%. The incidence rate was 29.6%, while the normalization rate was 26.4%, risk factors affecting incidence were age (OR=1.09, 95% CI: 1.03–1.17), baseline continuous values of metabolic syndrome risk scores (cMetS, OR=1.77, 95% CI:1.29–2.55) and baseline body weight (OR=1.06, 95% CI: 1.01–1.13). Normalization was influenced by age (OR=0.74, 95% CI: 0.57–0.89) and baseline body weight (OR=0.85, 95% CI: 0.72–0.95). CONCLUSION: The prevalence of MetS steadily increased with the continuous use of SGAs. However, individual difference was extensive and about a quarter of the patients were able to recover naturally without specific measurements. Korean Neuropsychiatric Association 2018-06 2018-06-21 /pmc/articles/PMC6018140/ /pubmed/29940717 http://dx.doi.org/10.30773/pi.2018.01.18.1 Text en Copyright © 2018 Korean Neuropsychiatric Association This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jeong, Seong Hoon
Lee, Nam Young
Kim, Se Hyun
Chung, In Won
Youn, Tak
Kang, Ung Gu
Ahn, Yong Min
You, Han Young
Kim, Yong Sik
Long-Term Evolution of Metabolic Status in Patients with Schizophrenia Stably Maintained on Second-Generation Antipsychotics
title Long-Term Evolution of Metabolic Status in Patients with Schizophrenia Stably Maintained on Second-Generation Antipsychotics
title_full Long-Term Evolution of Metabolic Status in Patients with Schizophrenia Stably Maintained on Second-Generation Antipsychotics
title_fullStr Long-Term Evolution of Metabolic Status in Patients with Schizophrenia Stably Maintained on Second-Generation Antipsychotics
title_full_unstemmed Long-Term Evolution of Metabolic Status in Patients with Schizophrenia Stably Maintained on Second-Generation Antipsychotics
title_short Long-Term Evolution of Metabolic Status in Patients with Schizophrenia Stably Maintained on Second-Generation Antipsychotics
title_sort long-term evolution of metabolic status in patients with schizophrenia stably maintained on second-generation antipsychotics
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018140/
https://www.ncbi.nlm.nih.gov/pubmed/29940717
http://dx.doi.org/10.30773/pi.2018.01.18.1
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