首页> 外文期刊>Journal of clinical psychopharmacology >The Relationships of Obesity-Related Genetic Variants With Metabolic Profiles and Response to Metformin in Clozapine-Treated Patients With Schizophrenia
【24h】

The Relationships of Obesity-Related Genetic Variants With Metabolic Profiles and Response to Metformin in Clozapine-Treated Patients With Schizophrenia

机译:肥胖相关基因变异与氯氮平治疗的精神分裂症患者代谢谱和对二甲双胍反应的关系

获取原文
获取原文并翻译 | 示例
           

摘要

Obesity-related genetic variants, including TMEM18 (rs6548238), SH2B1 (rs7498665), and GNPDA2 (rs10938397), have been shown to be associated with obesity in the general population. Our study aimed to test whether these genetic variants are associated with metabolic profiles and metformin treatment response in clozapine-treated schizophrenic patients. We recruited 107 clozapine-treated patients who were genotyped and measured their metabolic profiles. Fifty-five subjects, who had at least 1 metabolic abnormality in a range of measures, were subsequently randomized to a 24-week trial of metformin (n = 28) or placebo (n = 27). We examined the associations between TMEM18, SH2B1, GNPDA2 genetic variants and metabolic profiles at baseline in all patients and metabolic changes in the trial groups. We found a significant association between SH2B1 and blood pressure at baseline in all patients. In the metformin group, TMEM18 minor allele carriers had a greater reduction in insulin levels (P = 0.04). A significantly higher proportion of TMEM18 and GNPDA2 minor allele carriers (60% and 40%) lost more than 7% of their body weight after metformin treatment as compared with their homozygous counterparts (21.7% and 15.4%, P = 0.02 and 0.004, respectively). There were trends toward favorable metabolic changes in minor allele carrier groups. In the placebo group, no association between genetic variants and changes in metabolic profiles was found. In conclusion, the study results suggest that these genes might be associated with metabolic abnormalities and response to metformin in clozapine-treated patients with schizophrenia.
机译:肥胖相关的遗传变异体,包括TMEM18(rs6548238),SH2B1(rs7498665)和GNPDA2(rs10938397),已显示与普通人群的肥胖症有关。我们的研究旨在测试在氯氮平治疗的精神分裂症患者中这些遗传变异是否与代谢谱和二甲双胍治疗反应相关。我们招募了107名接受氯氮平治疗的患者,这些患者均经过了基因分型并测量了其代谢谱。 55名受试者在一系列测量中至少具有1种代谢异常,随后被随机分入二甲双胍(n = 28)或安慰剂(n = 27)的24周试验中。我们检查了所有患者在基线时TMEM18,SH2B1,GNPDA2遗传变异与代谢谱之间的关联以及试验组的代谢变化。我们发现在所有患者中,SH2B1与基线血压之间存在显着关联。在二甲双胍组中,TMEM18次要等位基因携带者的胰岛素水平降低幅度更大(P = 0.04)。与纯合子相比,二甲双胍治疗后,TMEM18和GNPDA2次要等位基因携带者失去体重的比例显着更高(60%和40%)(分别为21.7%和15.4%,P = 0.02和0.004) )。次要等位基因携带者群体中存在有利的代谢变化趋势。在安慰剂组中,未发现遗传变异与代谢谱变化之间的关联。总之,研究结果表明,这些基因可能与氯氮平治疗的精神分裂症患者的代谢异常和对二甲双胍的反应有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号