Association of polymorphisms in angiotensin II receptor gene with primary aldosteronism
Fu-Man Du, Weimin Wang, Binhong Duan, Chaofeng Xiang
Abstract
Fu-Man Du, Weimin Wang, Binhong Duan, Chaofeng Xiang
Abstract
Objective To investigate the relationship between the polymorphisms of angiotensin Ⅱ receptor gene and the risk of primary aldosteronism (PA). Methods Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was used to examine the 1166A/C polymorphism of AT1R gene and 1675A/G polymorphism of AT2R gene in 85 patients with PA and 100 healthy controls. Results There was no significant difference of AT1R 1166A/C genotypes (AA, AC, CC) and allele (A and C) frequency among patients and controls (χ2=0.430, P=0.806).There was obvious difference of AT2R 1675A/G genotypes (AA, AG, GG) and allele (A and G) frequency among two groups (χ2=6.121, P=0.013).The G allele was higher than A allele in PA group (χ2=6.767, P=0.009). Conclusion Homogenic mutation of 1675A/G site in AT2R gene may be one of risk factors of PA. Key words: Hyperaldosteronism; Receptor, angiotensin, type 2; Gene
A significance statement is not available in the OpenAlex record.
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 relationship between the polymorphisms of angiotensin Ⅱ receptor gene and the risk of primary aldosteronism (PA). Methods Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was used to examine the 1166A/C polymorphism of AT1R gene and 1675A/G polymorphism of AT2R gene in 85 patients with PA and 100 healthy controls. Results There was no significant difference of AT1R 1166A/C genotypes (AA, AC, CC) and allele (A and C) frequency among patients and controls (χ2=0.430, P=0.806).There was obvious difference of AT2R 1675A/G genotypes (AA, AG, GG) and allele (A and G) frequency among two groups (χ2=6.121, P=0.013).The G allele was higher than A allele in PA group (χ2=6.767, P=0.009). Conclusion Homogenic mutation of 1675A/G site in AT2R gene may be one of risk factors of PA. Key words: Hyperaldosteronism; Receptor, angiotensin, type 2; Gene
Key concepts: Genotype, Allele, Restriction fragment length polymorphism, Medicine, Internal medicine, Gene polymorphism, Endocrinology, Allele frequency