首页> 外文期刊>Experimental and clinical endocrinology and diabetes: Official journal, German Society of Endocrinology [and] German Diabetes Association >Analysis of the Relationship between PPAR-gamma 2 Gene Variants and Severe Insulin Resistance in Obese Patients with Impaired Glucose Tolerance.
【24h】

Analysis of the Relationship between PPAR-gamma 2 Gene Variants and Severe Insulin Resistance in Obese Patients with Impaired Glucose Tolerance.

机译:糖耐量减低的肥胖患者中PPAR-γ2基因变异与严重胰岛素抵抗之间的关系分析。

获取原文
获取原文并翻译 | 示例
           

摘要

Mutations in the peroxisome proliferator-activated receptor-gamma 2 (PPAR-gamma 2) gene may cause obesity and insulin resistance. Therefore we investigated whether known variants in the PPAR-gamma 2 gene are associated with obesity and extreme insulin resistance in obese patients with impaired glucose tolerance (IGT). The Pro115 Gln, Pro12Ala, Pro467Leu, Val290Met and a silent polymorphism C478 T were examined in 48 subjects with IGT and insulin resistance (IR), characterized by euglycemic hyperinsulinemic clamps, and in 52 healthy insulin sensitive (IS) controls. We found one proband in the IR group with the Pro115 Gln variant. This subject showed a lower whole body glucose uptake (18 micro mol/kg per min) compared to the entire IR group (29 micro mol/kg per min). The body weight of the proband (BMI 28.5 kg/m 2) was within the average of the IR group (30.3 +/- 0.8 kg/m 2). The Pro12Ala variant was not associated with differences in BMI, in the degree of insulin resistance between the IR and IS group. The Pro467Leu, Val290Met mutations and the silent polymorphism CAC478CAT were not detected in any group. In conclusion, the Pro115 Gln variant, but not the Pro12Ala mutation in the PPAR-gamma 2 gene, could be a rare cause of severe insulin resistance.
机译:过氧化物酶体增殖物激活的受体-γ2(PPAR-γ2)基因中的突变可能导致肥胖和胰岛素抵抗。因此,我们调查了糖耐量受损(IGT)肥胖患者中PPAR-γ2基因的已知变异是否与肥胖和极端胰岛素抵抗相关。在48位具有正常血糖高胰岛素钳夹特征的IGT和胰岛素抵抗(IR)的受试者和52位健康的胰岛素敏感(IS)对照中检查了Pro115 Gln,Pro12Ala,Pro467Leu,Val290Met和沉默多态性C478T。我们在IR组中发现了一个Pro115 Gln变体的先证者。与整个IR组(每分钟29 micro mol / kg)相比,该受试者的全身葡萄糖摄取量较低(每分钟18 micro mol / kg)。先证者的体重(BMI 28.5 kg / m 2)在IR组的平均值之内(30.3 +/- 0.8 kg / m 2)。 Pro12Ala变体与IR和IS组之间胰岛素抵抗程度的BMI差异无关。在任何组中均未检测到Pro467Leu,Val290Met突变和沉默多态性CAC478CAT。总之,Pro115 Gln变异体(而非PPAR-γ2基因中的Pro12Ala突变)可能是严重胰岛素抵抗的罕见原因。

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