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https://hdl.handle.net/11499/6677
Title: | The association of olanzapine-induced weight gain with peroxisome proliferator-activated receptor-?2 Pro12Ala polymorphism in patients with schizophrenia | Authors: | Herken, Hasan Erdal, M. Aydin, N. Sengul, C. Karadag, F. Barlas, O. Akın, Fulya |
Keywords: | alanine olanzapine peroxisome proliferator activated receptor gamma 2 proline adult aged amino acid substitution article body mass clinical evaluation diagnostic and statistical manual of mental disorders drug efficacy drug safety female gene expression genetic analysis genetic variability human major clinical study male priority journal rating scale schizophrenia side effect single nucleotide polymorphism treatment duration treatment outcome Turkey (republic) weight change weight gain Adult Alanine Antipsychotic Agents Base Sequence Benzodiazepines DNA Primers Humans Middle Aged PPAR gamma Proline Schizophrenia Weight Gain |
Abstract: | Olanzapine is a second-generation antipsychotic that may cause weight gain and metabolic syndrome in some cases. The peroxisome proliferator-activated receptor (PPAR)-? is an important gene in the progress of type II diabetes and metabolic syndrome. In recent studies the polymorphism of the PPAR-? has been studied in type II diabetes mellitus, polycystic ovary syndrome, and insulin resistance syndrome. It is aimed to evaluate the association between polymorphism of PPAR-? gene and olanzapine-induced weight gain. Our study comprised 95 unrelated subjects who strictly met Diagnostic and Statistical Manual of Mental Disorders, 4th edition (DSM-IV) criteria for schizophrenia, and all were of Turkish origin. All patients were evaluated with rating scales, and genetic analyses were performed. We found statistically significant differences between pretreatment and posttreatment body mass index and weight change in Pro12Ala polymorphism of PPAR-?2. Our results suggest that genetic polymorphism of PPAR might be important in olanzapine-induced weight gain and that genetic variance of people might be considered in antipsychotic medication selection. © 2009 Mary Ann Liebert, Inc. | URI: | https://hdl.handle.net/11499/6677 https://doi.org/10.1089/dna.2009.0893 |
ISSN: | 1044-5498 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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