The association of hypertension with renin-angiotensin system gene polymorphisms in the Lebanese population

被引:20
作者
Saab, Y. B. [1 ]
Gard, P. R. [2 ]
Overall, A. D. J. [2 ]
机构
[1] Lebanese Amer Univ, Sch Pharm, Byblos, Lebanon
[2] Univ Brighton, Brighton BN2 4AT, E Sussex, England
关键词
Angiotensin converting enzyme; angiotensin receptor type 1; angiotensinogen; gene; hypertension; polymorphism; CONVERTING-ENZYME GENE; ACE INSERTION/DELETION POLYMORPHISM; TYPE-1 RECEPTOR GENE; BLOOD-PRESSURE; DELETION POLYMORPHISM; ALDOSTERONE SYSTEM; RISK; DISEASE; M235T; I/D;
D O I
10.1177/1470320311408465
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Aim: The study objective was to examine the association of hypertension in the Lebanese population with three renin-angiotensin system gene polymorphisms (RAS): angiotensin-converting enzyme (ACE), angiotensinogen (AGT) and angiotensin-receptor type 1 (AT1R). Methods: A total of 270 subjects (124 hypertensive vs 146 normotensive) were genotyped for ACE insertion (I)/deletion (D), AGT (M235T), and AT(1)R (A1166C) gene polymorphisms by polymerase chain reaction and restriction fragment length polymorphism. Results: The studied genes showed no deviation from Hardy-Weinberg equilibrium. No association could be reported with the ACE I/D polymorphism, although the D allele frequency was high (77%) in patients. AGT TT genotype prevalence was found to be lower in hypertensive versus normotensive subjects (p < 0.0001). AT(1)R CC and AC genotypes were significantly more frequent in hypertensive than normotensive subjects (p < 0.0001). Conclusion: The first conducted study on the RAS gene polymorphisms in Lebanese hypertensive patients demonstrated a possible association of the AGT T and AT(1)R C alleles with hypertension.
引用
收藏
页码:588 / 594
页数:7
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