巴基斯坦人口中维斯法基因多态与肥胖相关代谢障碍的关联:一个病例对照研究
Sayyada Humaira Masood1,2, Taseer Ahmed Khan3, Akhter Ali Baloch4
1Department of Physiology, University of Karachi, Karachi, Pakistan. sayyadahumaira23@gmail.com.
Scientific reports
|December 28, 2023
概括
视法丁的遗传变异,特别是SNP rs2302559和rs1215113036,与患代谢综合征的风险增加有显著联系. 这些visfatin遗传变异在疾病中发挥着作用.
科学领域:
- 遗传学 是一个遗传学.
- 代谢障碍 代谢障碍 代谢障碍
- 内分泌学 在内分泌学.
背景情况:
- 肥胖和代谢障碍构成了全球卫生挑战.
- 维斯法丁 (PBEF/NAMPT) 是一种参与葡萄糖,脂质和炎症调节的阿迪波金.
研究的目的:
- 调查visfatin遗传变异与代谢综合征之间的关联.
主要方法:
- 用300个血液样本 (150个病例,150个对照) 进行病例控制研究.
- 对visfatin单核酸多态 (SNP) 的基因型频率的分析.
主要成果:
- 在视沙丁SNPrs2302559和rs1215113036与代谢综合征之间发现了显著的关联.
- 与对照组相比,在代谢综合征患者中,这些SNP的突变等位基因的频率更高.
- 赔率比:rs2302559 (18.222) 和rs1215113036 (129.40),两者均为p < 0.001.1. 这两种赔率比均为p < 0.001.
结论:
- 包括rs2302559和rs1215113036在内的Visfatin遗传变异与代谢综合征的风险增加有关.
- 这些发现表明visfatin在代谢综合征的病理生理学中的作用.
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