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首页> 外文期刊>Human psychopharmacology: clinical and experimental >Exploratory study on association of genetic variation in TBC1D1 with antipsychotic-induced weight gain
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Exploratory study on association of genetic variation in TBC1D1 with antipsychotic-induced weight gain

机译:探索性研究协会的基因变异与antipsychotic-induced TBC1D1体重增加

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摘要

Background Previous studies have shown that antipsychotics with high propensity for antipsychotic-induced weight gain (AIWG) influence glucose transporter type 4 (GLUT4) mediated glucose intake. Variation in the gene encoding TBC1 domain family member 1 (TBC1D1), a Rab-GTPase activating protein regulating GLUT4 trafficking, has been associated with obesity. Therefore, we investigated the impact of TBC1D1 polymorphisms on AIWG. Methods We analyzed rs9852 and rs35859249 in TBC1D1 in 195 schizophrenia subjects treated mostly with clozapine or olanzapine for up to 14 weeks. Association was tested using analysis of variance and analysis of covariance with change (%) from baseline weight as the dependent variable. Results Analysis of covariance showed a non-significant trend for lower weight gain in carriers of the T-allele of rs9852 than in C-allele homozygotes (p = 0.063). This effect was more pronounced in the subgroup of patients treated with clozapine or olanzapine (p = 0.024). For rs35859249, no significant association with AIWG could be detected. Conclusions This is the first study examining the association between TBC1D1 and AIWG. The moderate association of rs9852, located in the 3′UTR near a miRNA binding site, indicates an influence of TBC1D1 on AIWG. Further investigations remain necessary to elucidate the role of this gene in AIWG.
机译:之前的研究表明,背景抗精神病药物高倾向antipsychotic-induced体重增加(AIWG)影响葡萄糖转运体类型4 (GLUT4)调节葡萄糖的摄入。编码TBC1域家庭成员1 (TBC1D1)Rab-GTPase激活调节GLUT4蛋白交易,与肥胖有关。因此,我们调查了TBC1D1的影响AIWG多态性。和195年在TBC1D1 rs35859249精神分裂症受试者大多与氯氮平治疗奥氮平14周。使用方差分析进行了测试和分析协方差基准体重的变化(%)作为因变量。协方差显示非重要趋势低体重T-allele的运营商rs9852比C-allele比如(p = 0.063)。这种效应更加明显的子群与氯氮平或奥氮平治疗的患者(p = 0.024)。与AIWG可被检测到。这是第一个研究结论TBC1D1和AIWG之间的联系。rs9852协会位于3 'utr近了microrna的结合位点,表明一个的影响TBC1D1 AIWG。有必要阐明这种基因的作用

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