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G-protein β3 Subunit Gene 825C/T Polymorphism Is Not Associated with Olanzapine-Induced Weight Gain in Korean Schizophrenic Patients

OBJECTIVE: Weight gain is a possible adverse effect of the use of antipsychotics, and is an important factor for long-term health and treatment compliance. Olanzapine is an atypical antipsychotic known to cause considerable weight gain. A relationship between weight gain and the G protein β3 subunit...

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Autores principales: Park, Young-Min, Chung, Young-Cho, Lee, Seung-Hwan, Lee, Kang-Joon, Kim, Hyun, Choi, Jung-Eun, Kang, Seung-Gul, Lee, Min-Soo, Kim, Leen, Lee, Heon-Jeong
Formato: Texto
Lenguaje:English
Publicado: Korean Neuropsychiatric Association 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796038/
https://www.ncbi.nlm.nih.gov/pubmed/20046372
http://dx.doi.org/10.4306/pi.2009.6.1.39
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author Park, Young-Min
Chung, Young-Cho
Lee, Seung-Hwan
Lee, Kang-Joon
Kim, Hyun
Choi, Jung-Eun
Kang, Seung-Gul
Lee, Min-Soo
Kim, Leen
Lee, Heon-Jeong
author_facet Park, Young-Min
Chung, Young-Cho
Lee, Seung-Hwan
Lee, Kang-Joon
Kim, Hyun
Choi, Jung-Eun
Kang, Seung-Gul
Lee, Min-Soo
Kim, Leen
Lee, Heon-Jeong
author_sort Park, Young-Min
collection PubMed
description OBJECTIVE: Weight gain is a possible adverse effect of the use of antipsychotics, and is an important factor for long-term health and treatment compliance. Olanzapine is an atypical antipsychotic known to cause considerable weight gain. A relationship between weight gain and the G protein β3 subunit gene (GNB3) 825C/T polymorphism has been reported. We therefore examined this possible association in a Korean schizophrenic patient group receiving olanzapine treatment. METHODS: Weight and height measurements were obtained prior to starting olanzapine and measured again after long-term treatment. Genotyping for the 825C/T polymorphism was performed using a PCR-based method. RESULTS: We found that long-term treatment with olanzapine resulted in mean gains in weight and body mass index (BMI) of 5.2 kg and 1.93 kg/m(2), respectively. There was a no significant difference in the mean body weight change from baseline to the endpoint after olanzapine treatment between the genotype groups (p=0.796). There were also no significant differences in genotype or allele frequencies between the severe weight-gain (more than 10%) and minimal weight-gain (less than 10%) groups (χ(2)=0.037, p=0.98; χ(2)=0.020, p=0.89). CONCLUSION: The finding from this study thus does not support a relationship between the GNB3 825C/T polymorphism and weight gain in Korean schizophrenic patients receiving olanzapine treatment.
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spelling pubmed-27960382009-12-30 G-protein β3 Subunit Gene 825C/T Polymorphism Is Not Associated with Olanzapine-Induced Weight Gain in Korean Schizophrenic Patients Park, Young-Min Chung, Young-Cho Lee, Seung-Hwan Lee, Kang-Joon Kim, Hyun Choi, Jung-Eun Kang, Seung-Gul Lee, Min-Soo Kim, Leen Lee, Heon-Jeong Psychiatry Investig Original Article OBJECTIVE: Weight gain is a possible adverse effect of the use of antipsychotics, and is an important factor for long-term health and treatment compliance. Olanzapine is an atypical antipsychotic known to cause considerable weight gain. A relationship between weight gain and the G protein β3 subunit gene (GNB3) 825C/T polymorphism has been reported. We therefore examined this possible association in a Korean schizophrenic patient group receiving olanzapine treatment. METHODS: Weight and height measurements were obtained prior to starting olanzapine and measured again after long-term treatment. Genotyping for the 825C/T polymorphism was performed using a PCR-based method. RESULTS: We found that long-term treatment with olanzapine resulted in mean gains in weight and body mass index (BMI) of 5.2 kg and 1.93 kg/m(2), respectively. There was a no significant difference in the mean body weight change from baseline to the endpoint after olanzapine treatment between the genotype groups (p=0.796). There were also no significant differences in genotype or allele frequencies between the severe weight-gain (more than 10%) and minimal weight-gain (less than 10%) groups (χ(2)=0.037, p=0.98; χ(2)=0.020, p=0.89). CONCLUSION: The finding from this study thus does not support a relationship between the GNB3 825C/T polymorphism and weight gain in Korean schizophrenic patients receiving olanzapine treatment. Korean Neuropsychiatric Association 2009-03 2009-03-31 /pmc/articles/PMC2796038/ /pubmed/20046372 http://dx.doi.org/10.4306/pi.2009.6.1.39 Text en Copyright © 2009 Official Journal of Korean Neuropsychiatric Association http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Park, Young-Min
Chung, Young-Cho
Lee, Seung-Hwan
Lee, Kang-Joon
Kim, Hyun
Choi, Jung-Eun
Kang, Seung-Gul
Lee, Min-Soo
Kim, Leen
Lee, Heon-Jeong
G-protein β3 Subunit Gene 825C/T Polymorphism Is Not Associated with Olanzapine-Induced Weight Gain in Korean Schizophrenic Patients
title G-protein β3 Subunit Gene 825C/T Polymorphism Is Not Associated with Olanzapine-Induced Weight Gain in Korean Schizophrenic Patients
title_full G-protein β3 Subunit Gene 825C/T Polymorphism Is Not Associated with Olanzapine-Induced Weight Gain in Korean Schizophrenic Patients
title_fullStr G-protein β3 Subunit Gene 825C/T Polymorphism Is Not Associated with Olanzapine-Induced Weight Gain in Korean Schizophrenic Patients
title_full_unstemmed G-protein β3 Subunit Gene 825C/T Polymorphism Is Not Associated with Olanzapine-Induced Weight Gain in Korean Schizophrenic Patients
title_short G-protein β3 Subunit Gene 825C/T Polymorphism Is Not Associated with Olanzapine-Induced Weight Gain in Korean Schizophrenic Patients
title_sort g-protein β3 subunit gene 825c/t polymorphism is not associated with olanzapine-induced weight gain in korean schizophrenic patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796038/
https://www.ncbi.nlm.nih.gov/pubmed/20046372
http://dx.doi.org/10.4306/pi.2009.6.1.39
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