LAUSR

Objectives: Because heritability had remarkable effects on circulating ACE2, we designed this study to shed light on whether circulating levels of ACE2, angiotensin- (1- 7) and angiotensin- (1- 9) were linked to single nucleotide polymorphisms (SNPs) and haplotypes in ACE2 gene. Methods: A total of 213 patients with newly diagnosed mild to moderate EH were enrolled in the present study. Four ACE2 tag SNPs (rs2074192, rs4646171, rs4646155 and rs2106809) were genotyped, and major haplotypes consisting of these 4 SNPs were reconstructed for all subjects. Circulating levels of ACE2, angiotensin- (1- 7) and angiotensin- (1- 9) were measured using enzyme- linked immunosorbent assay Results: In female subjects, linear regression analysis suggested that rare alleles of ACE2 rs2074192 and rs2106809 were associated with reduced circulating angiotensin-(1- 7) levels (P = .007 and P = .006, respectively). ACE2 haplotype CAGC was associated with elevated circulating angiotensin- (1- 7) levels (P = .03) whereas TAGT was associated with reduced circulating angiotensin- (1- 7) levels in females (P < .001). Univariate linear regression analysis revealed that circulating ACE2 levels were positively associated with systolic blood pressure (P = .02), mean arterial pressure (P = .02) and serum creatinine (P < .001) in females whereas circulating ACE2 levels were positively associated with age (P < .001) and serum creatinine (P < .001) in males Conclusion: ACE2 SNPs and haplotypes are associated with circulating angiotensin- (1- 7) levels. ACE2 genetic variants may be the determinants of circulating angiotensin- (1- 7) levels in hypertensive females.