...
首页> 外文期刊>Pharmacological research: The official journal of The Italian Pharmacological Society >Interleukin-1 (IL-1) receptor antagonist gene polymorphism in normal weight obese syndrome: Relationship to body composition and IL-1 alpha and beta plasma levels.
【24h】

Interleukin-1 (IL-1) receptor antagonist gene polymorphism in normal weight obese syndrome: Relationship to body composition and IL-1 alpha and beta plasma levels.

机译:正常体重肥胖综合征中白细胞介素-1(IL-1)受体拮抗剂基因多态性:与身体成分以及IL-1α和β血浆水平的关系。

获取原文
获取原文并翻译 | 示例

摘要

Interleukin-1 receptor antagonist concentration is upregulated in the plasma of patients with obese related disease, and its synthesis is under genetic control. We tested the hypothesis that the polymorphism in the interleukin-1 receptor antagonist gene second intron might be associated with normal weight obese syndrome. The polymorphism of intron 2 in the interleukin-1 receptor antagonist gene, containing a variable numbers of a tandem repeat (VNTR), and interleukin-1alpha and beta plasma levels were evaluated in 110 Caucasian Italian women, divided in three groups: non-obese, normal weight obese and preobese-obese. The allele 1 frequency was not significantly different in the three groups. The alleles 3 and 4 were not observed in any group. The allele 2 frequency in normal weight obese woman (12.5%) and preobese-obese (17.5%) groups were significantly different in comparison with the non-obese group (6.7%). The allele 5 was observed exclusively in non-obese and normal weight obese subjects (13.3 and 7.5%, respectively). In normal weight obese women, plasma concentrations of interleukin-1 alpha and interleukin-1 beta were significantly higher than in non-obese. The allele 2 was observed in normal weight obese as well as a significant association between the increase of interleukin-1 beta plasma amount and the allele 2 carrier. Our findings suggest that the allele 2 might be an important high-risk genetic marker for normal weight obese syndrome and obesity related diseases.
机译:肥胖相关疾病患者血浆中白介素-1受体拮抗剂的浓度上调,并且其合成处于遗传控制之下。我们检验了白介素1受体拮抗剂基因第二个内含子的多态性可能与正常体重肥胖综合征相关的假设。在110名意大利白人女性中评估了白细胞介素1受体拮抗剂基因中内含子2的多态性,该基因包含可变数目的串联重复(VNTR)以及白细胞介素1α和β血浆水平,分为三组:非肥胖,正常体重肥胖和肥胖前期肥胖。在三组中,等位基因1的频率没有显着差异。在任何组中均未观察到等位基因3和4。正常体重肥胖妇女(12.5%)和肥胖前肥胖(17.5%)组的等位基因2频率与非肥胖组(6.7%)相比有显着差异。仅在非肥胖和正常体重的肥胖受试者中观察到等位基因5(分别为13.3和7.5%)。在正常体重的肥胖妇女中,白细胞介素-1α和白介素-1β的血浆浓度显着高于非肥胖者。在体重正常的肥胖者中观察到等位基因2,并且在白介素-1β血浆量的增加与等位基因2载体之间发现显着关联。我们的研究结果表明,等位基因2可能是正常体重肥胖综合征和肥胖相关疾病的重要高风险遗传标志。

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