BACKGROUND: ATP1B1 encodes the beta subunits of Na/K ATPase which plays an important role in maintaining the normal gradients of Na(+) and K(+) across plasma membrane. A recent study demonstrated an association of ATP1B1 genetic variations with blood pressure (BP) in Americans. We aimed to investigate the association between ATP1B1 polymorphisms with BP and hypertension in a Chinese population. MATERIAL AND METHODS: Twelve tag single-nucleotide polymorphisms (SNPs) of ATP1B1 were genotyped in 906 patients with essential hypertension (EH) and 894 normotensives (NT). RESULTS: None of the selected SNPs was associated with hypertension. However, an overall significant association of haplotypes containing rs1200131, rs1200137, rs3766032, rs3766039 and rs2982468 with hypertension was observed (p=0.032). A common haplotype (G-T-A-C-T) was associated with an increased risk for hypertension (OR(adjusted)=1.717, p=0.033). In NT subjects, rs3766032AA carriers had lower systolic BP (SBP) and diastolic BP (DBP) than AG/GG carriers (SBP, 112.6+/-10.0 mmHg vs. 115.5+/-10.6 mmHg, p<0.05; DBP, 75.1+/-6.8 mmHg vs. 76.8+/-6.0 mmHg, p<0.05), and rs2982468 TT carriers had lower DBP than AT/AA carriers (74.8+/-6.9 mmHg vs. 76.3+/-6.2 mmHg; p<0.01) after correction. In NT subjects, BP showed an overall significant association with haplotypes (p=0.006, for SBP and p=0.036, for DBP). CONCLUSION: We conclude that haplotype in ATP1B1 may confer susceptibility to BP regulation and hypertension in this Chinese population.
BACKGROUND:ATP1B1 encodes the beta subunits of Na/K ATPase which plays an important role in maintaining the normal gradients of Na(+) and K(+) across plasma membrane. A recent study demonstrated an association of ATP1B1 genetic variations with blood pressure (BP) in Americans. We aimed to investigate the association between ATP1B1 polymorphisms with BP and hypertension in a Chinese population. MATERIAL AND METHODS: Twelve tag single-nucleotide polymorphisms (SNPs) of ATP1B1 were genotyped in 906 patients with essential hypertension (EH) and 894 normotensives (NT). RESULTS: None of the selected SNPs was associated with hypertension. However, an overall significant association of haplotypes containing rs1200131, rs1200137, rs3766032, rs3766039 and rs2982468 with hypertension was observed (p=0.032). A common haplotype (G-T-A-C-T) was associated with an increased risk for hypertension (OR(adjusted)=1.717, p=0.033). In NT subjects, rs3766032AA carriers had lower systolic BP (SBP) and diastolic BP (DBP) than AG/GG carriers (SBP, 112.6+/-10.0 mmHg vs. 115.5+/-10.6 mmHg, p<0.05; DBP, 75.1+/-6.8 mmHg vs. 76.8+/-6.0 mmHg, p<0.05), and rs2982468 TT carriers had lower DBP than AT/AA carriers (74.8+/-6.9 mmHg vs. 76.3+/-6.2 mmHg; p<0.01) after correction. In NT subjects, BP showed an overall significant association with haplotypes (p=0.006, for SBP and p=0.036, for DBP). CONCLUSION: We conclude that haplotype in ATP1B1 may confer susceptibility to BP regulation and hypertension in this Chinese population.
Authors: Mezbah U Faruque; Guanjie Chen; Ayo Doumatey; Hanxia Huang; Jie Zhou; Georgia M Dunston; Charles N Rotimi; Adebowale A Adeyemo Journal: J Hypertens Date: 2011-10 Impact factor: 4.844
Authors: Megana K Prasad; Kavita Bhalla; Zhen Hua Pan; Jeffrey R O'Connell; Alan B Weder; Aravinda Chakravarti; Bin Tian; Yen-Pei C Chang Journal: PLoS One Date: 2013-10-01 Impact factor: 3.240