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清道夫受体 B 类 1 型的表达水平和遗传多态性作为 2 型糖尿病的生物标志物。

Expression Levels and Genetic Polymorphism of Scavenger Receptor Class B Type 1 as a Biomarker of Type 2 Diabetes Mellitus.

机构信息

Department of Pathology, King George's Medical University, Lucknow, India.

Department of Medicine, King George's Medical University, Lucknow, India.

出版信息

Sultan Qaboos Univ Med J. 2022 Feb;22(1):117-122. doi: 10.18295/squmj.4.2021.042. Epub 2022 Feb 28.

Abstract

OBJECTIVES

This study aimed to determine whether the expression level and genetic polymorphism scavenger receptor class B type 1 () rs5888 may be used as biological markers in type 2 diabetes mellitus (T2DM).

METHODS

This case-control study was conducted at King George's Medical University, Lucknow, India, from September 2018 to December 2019. Blood samples were collected from each individual with T2DM and each healthy individual. Total proteins were determined using western blot analysis. Additionally, restriction fragment length polymorphism analysis was achieved to detect the incidence of genetic polymorphisms.

RESULTS

A total of 600 individuals, including 300 individuals with T2DM and 300 healthy individuals, were enrolled in the study. Western blot analysis results revealed that the protein expression of SRB1 was significantly decreased in T2DM of CC variant when compared with controls ( = 0.007). The genotype distribution and the allelic frequencies for the SRB1 polymorphism were significantly different between T2DM and controls ( = 0.03). The CC genotype of the polymorphism showed a potential association with the incidence of T2DM (odds ratio = 1.19, 95% confidence interval = 0.63-2.25; = 0.577).

CONCLUSION

The expression levels and genetic polymorphisms of the CC variant may be potential biomarkers for the occurrence of T2DM.

摘要

目的

本研究旨在确定清道夫受体 B 类 1()基因 rs5888 的表达水平和遗传多态性是否可作为 2 型糖尿病(T2DM)的生物标志物。

方法

该病例对照研究于 2018 年 9 月至 2019 年 12 月在印度勒克瑙的乔治国王医科大学进行。从每位 T2DM 患者和每位健康个体采集血样。采用 Western blot 分析测定总蛋白。此外,还进行了限制性片段长度多态性分析以检测遗传多态性的发生率。

结果

共纳入 600 名个体,包括 300 名 T2DM 患者和 300 名健康个体。Western blot 分析结果显示,与对照组相比,T2DM 患者中 CC 变异型的 SRB1 蛋白表达显著降低(=0.007)。SRB1 多态性的基因型分布和等位基因频率在 T2DM 患者和对照组之间存在显著差异(=0.03)。多态性的 CC 基因型与 T2DM 的发生具有潜在相关性(比值比=1.19,95%置信区间=0.63-2.25;=0.577)。

结论

CC 变异型的表达水平和遗传多态性可能是 T2DM 发生的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e741/8904105/b131f8206e45/squmj2202-117-122f1.jpg

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