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Association study of polymorphisms in Insulin Induced Gene 2 (INSIG2) with antipsychotic‐induced weight gain in European and African‐American schizophrenia patients
Author(s) -
Tiwari Arun K.,
Zai Clement C.,
Meltzer Herbert Y.,
Lieberman Jeffrey A.,
Müller Daniel J.,
Kennedy James L.
Publication year - 2010
Publication title -
human psychopharmacology: clinical and experimental
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.461
H-Index - 78
eISSN - 1099-1077
pISSN - 0885-6222
DOI - 10.1002/hup.1111
Subject(s) - clozapine , olanzapine , risperidone , antipsychotic , weight gain , haloperidol , allele , medicine , genotype , schizophrenia (object oriented programming) , oncology , endocrinology , genetics , psychiatry , biology , gene , dopamine , body weight
Objective Atypical antipsychotic drugs, in particular clozapine and olanzapine, influence cellular lipogenesis and are associated with metabolic side effects including weight gain. Insulin induced gene 2 (INSIG2) mediates feedback control of lipid synthesis and polymorphisms in the gene (rs17587100, rs10490624 and rs17047764) have been associated with antipsychotic induced weight gain. In this study we intended to replicate these findings in an independent patient population. Methods All three polymorphisms as well as an additional polymorphism (rs7566605) were genotyped in 154 patients who underwent treatment for chronic schizophrenia with one of four antipsychotics (clozapine, olanzapine, haloperidol or risperidone). Patients were evaluated for antipsychotic induced weight gain during treatment for up to 14 weeks. Results We did not observe any significant allelic, genotypic or haplotypic association of the polymorphisms with antipsychotic induced weight gain in the patients of European ancestry ( p > 0.05). In the patients of African ancestry, no haplotypic association was observed but a trend of allelic association with the C allele of rs7566605 and genotypic association with the ‘GC’ genotype in rs17047764 was observed ( p = 0.02; p Bonferroni = 0.225). Conclusion We were unable to replicate significant associations in patients of European ancestry. However, we observed a marginal effect of the rs17047764 and rs7566605 in the African‐American sample. Since the latter observations were generated in a relatively small sample set, further replication studies are warranted. Copyright © 2010 John Wiley & Sons, Ltd.