Please use this identifier to cite or link to this item: 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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