Association between E-selectin gene polymorphism and essential hypertension in Hani minority
Qian Zhang
Abstract
Qian Zhang
Abstract
Objective:To investigate the association between four missense mutation in E-selectin gene including rs3917408 G/T,rs5361 A/C,rs3917429 C/T and rs5355 C/T and essential hypertension in Hani minority.Methods:E-selectin genotyped by sequence was performed in 133 normotensive subjects and 172 essential hypertensive subjects.Results:The allele frequency of the four studied polymorphism in normotensive controls and essential hypertensive cohort in Hani population were rs3917408 T:0.004vs.0.020;rs5361 C:0.049 vs 0.070;rs5368 T:0.218 vs.0.288;rs3917429 T:0.011 vs.0.061,respectively.The frequency of rs3917429 T allele in the essential hypertensive group was significantly higher than that in the normotensive controls(P0.01).No significant difference was found between the two groups in the other loci.Conclusion:The rs3917429 T allele of the E-selectin gene may play a role in genetic predisposition to developing essential hypertension in Hani minorities.
OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective:To investigate the association between four missense mutation in E-selectin gene including rs3917408 G/T,rs5361 A/C,rs3917429 C/T and rs5355 C/T and essential hypertension in Hani minority.Methods:E-selectin genotyped by sequence was performed in 133 normotensive subjects and 172 essential hypertensive subjects.Results:The allele frequency of the four studied polymorphism in normotensive controls and essential hypertensive cohort in Hani population were rs3917408 T:0.004vs.0.020;rs5361 C:0.049 vs 0.070;rs5368 T:0.218 vs.0.288;rs3917429 T:0.011 vs.0.061,respectively.The frequency of rs3917429 T allele in the essential hypertensive group was significantly higher than that in the normotensive controls(P0.01).No significant difference was found between the two groups in the other loci.Conclusion:The rs3917429 T allele of the E-selectin gene may play a role in genetic predisposition to developing essential hypertension in Hani minorities.
Key concepts: Essential hypertension, Allele, Missense mutation, Polymorphism (computer science), Genetics, Allele frequency, Internal medicine, Gene