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首页> 外文期刊>Human psychopharmacology: clinical and experimental >Association study of polymorphisms in Insulin Induced Gene 2 (INSIG2) with antipsychotic-induced weight gain in European and African-American schizophrenia patients
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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

机译:协会的多态性研究胰岛素诱导基因2 (INSIG2仅)在欧洲,antipsychotic-induced体重增加非裔美国人的精神分裂症患者

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Objective Atypical antipsychotic drugs, in particular clozapine and olanzapine, influence cellular Epogenesis 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 (rsl7587100, rs10490624 and rsl7047764) 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 rsl7047764 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.
机译:客观的非典型抗精神病药物特定的氯氮平、奥氮平的影响细胞Epogenesis和相关联代谢副作用包括体重增加。胰岛素诱导基因2 (INSIG2仅)介导的反馈控制的脂质合成和多态性基因(rsl7587100 rs10490624和rsl7047764)与抗精神病药物诱导有关吗体重增加。这些发现在一个独立的复制病人的人口。多态性以及额外的154年多态性(rs7566605)基因分型病人治疗慢性精神分裂症的四抗精神病药物(氯氮平、奥氮平、氟哌啶醇或利培酮)。抗精神病药物诱导期间体重增加治疗14周。观察任何重要的等位基因,基因型或haplotypic协会的多态性抗精神病药物引起体重增加的病人欧洲血统(p > 0.05)。的非洲血统,没有haplotypic协会观察等位基因关联的趋势呢rs7566605的C等位基因和基因型的与rsl7047764 GC的基因型观察(p = 0.02;结论我们无法复制欧洲的重要关联的病人血统。rs17047764和rs7566605非裔美国人的样本。观察在一个相对较小的生成样本集,进一步复制研究必要的。

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