Abstract
Abstract
Background
Scavenger receptor class B, type I (SR-BI), involved in reverse cholesterol pathway, is a multilipoprotein receptor and capable of binding HDL, LDL and VLDL. SR-BI may contribute to the development of hypertension due to accumulation of cholesterol in the vessel wall via transporting lipoproteins. Therefore, it was aimed to investigate the relationship between SR-BI rs5888 and rs4238001 variants in the patient with hypertension.
Materials and methods
Seventy three subjects diagnosed with hypertension and 76 healthy subjects constituted the patient and control group, respectively. Genomic DNA was isolated from peripheral blood samples and a real-time quantitative polymerase chain reaction protocol was performed to detect variations of rs5888 and rs4238001. The results were analyzed with the SPSS 22 program and p < 0.05 was considered statistically significant.
Results and discussion
SR-BI rs4238001 variation did not show significant difference between patient and control group (p > 0.05). In the SR-BI rs5888 variation; normal homozygous CC and heterozygous CT carriers had an average 2-fold lower risk of hypertension than those carrying the TT genotype (p < 0.05).
Conclusion
SR-BI rs5888 TT variant may increase hypertension risk by reducing lipid transport to the liver from the vessel wall.
Subject
Biochemistry, medical,Clinical Biochemistry,Molecular Biology,Biochemistry
Reference52 articles.
1. High density lipoprotein uptake by scavenger receptor SR-BII;J Biol Chem,2004
2. Lipid free apolipoprotein E binds to the class B Type I scavenger receptor I (SR-BI) and enhances cholesteryl ester uptake from lipoproteins;J Biol Chem,2002
3. SR-BI: linking cholesterol and lipoprotein metabolism with breast and prostate cancer;Front Pharmacol,2016
4. Apolipoprotein A-I conformation markedly influences HDL interaction with scavenger receptor BI;J Lipid Res,2001
5. Factors affecting hypertension and blood pressure in the community;Bes Diy Derg,2017
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