A core promoter variant of angiotensinogen gene and interindividual variation in response to angiotensin-converting enzyme inhibitors
Introduction: The polymorphic angiotensinogen (AGT) gene is one of the most promising candidates for essential hypertension. The aim of this study was to examine the association between the A-6G variant of the AGT gene and the blood pressure response to angiotensin-converting enzyme (ACE) inhibitors...
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doaj-fef95814c2c54a7c8176434ba92ec2e42021-05-02T09:35:32ZengHindawi - SAGE PublishingJournal of the Renin-Angiotensin-Aldosterone System1470-32031752-89762014-12-011510.1177/1470320313506481A core promoter variant of angiotensinogen gene and interindividual variation in response to angiotensin-converting enzyme inhibitorsHuimin Yu0Shuguang Lin1Jiuchang Zhong2Min He3Lijun Jin4Yuqing Zhang5Guozhang Liu6Department of Cardiology, Guangdong General Hospital, China; Guangdong Academy of Medical Sciences, ChinaDepartment of Cardiology, Guangdong General Hospital, China; Guangdong Academy of Medical Sciences, ChinaState Key Laboratory of Medical Genomics, Ruijin Hospital affiliated to Shanghai Jiao Tong University School of Medicine, China; Shanghai Institute of Hypertension, ChinaDepartment of Clinical Laboratory, Guangdong Provincial Hospital of Chinese Medicine, ChinaDepartment of Cardiology, Guangdong General Hospital, China; Guangdong Academy of Medical Sciences, ChinaDivision of Hypertension, Cardiovascular Institute and Fu Wai Hospital, Chinese Academy of Medical Sciences, China; Peking Union Medical College, ChinaDivision of Hypertension, Cardiovascular Institute and Fu Wai Hospital, Chinese Academy of Medical Sciences, China; Peking Union Medical College, ChinaIntroduction: The polymorphic angiotensinogen (AGT) gene is one of the most promising candidates for essential hypertension. The aim of this study was to examine the association between the A-6G variant of the AGT gene and the blood pressure response to angiotensin-converting enzyme (ACE) inhibitors in hypertensive subjects. Methods: Five hundred and nine mildly to moderately hypertensive subjects received ACE inhibitors for six weeks after a two-week run-in period. AGT genotyping was performed by direct polymerase chain reaction amplification and deoxyribonucleic acid (DNA) nucleotide sequencing from peripheral blood. Results: The AA genotype, AG genotype, and GG genotype were present in 301 (59.1%), 186 (36.6%), and 22 (4.3%) of patients, respectively. As compared with patients carrying the AA or AG genotype, those carrying the GG genotype had significantly greater reductions in systolic blood pressure, diastolic blood pressure, pulse pressure and mean arterial pressure ( p =0.007, 0.014, 0.027 and 0.005, respectively). Moreover, stepwise multiple linear regression analysis showed that the A-6G genotype was a significant predictor of systolic blood pressure and pulse pressure reductions ( p= 0.040 and 0.019, respectively). Conclusion: Our study indicates that the A-6G variant of the AGT gene may be an important determinant of interindividual variation in the response to ACE inhibitors.https://doi.org/10.1177/1470320313506481 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Huimin Yu Shuguang Lin Jiuchang Zhong Min He Lijun Jin Yuqing Zhang Guozhang Liu |
spellingShingle |
Huimin Yu Shuguang Lin Jiuchang Zhong Min He Lijun Jin Yuqing Zhang Guozhang Liu A core promoter variant of angiotensinogen gene and interindividual variation in response to angiotensin-converting enzyme inhibitors Journal of the Renin-Angiotensin-Aldosterone System |
author_facet |
Huimin Yu Shuguang Lin Jiuchang Zhong Min He Lijun Jin Yuqing Zhang Guozhang Liu |
author_sort |
Huimin Yu |
title |
A core promoter variant of angiotensinogen gene and interindividual variation in response to angiotensin-converting enzyme inhibitors |
title_short |
A core promoter variant of angiotensinogen gene and interindividual variation in response to angiotensin-converting enzyme inhibitors |
title_full |
A core promoter variant of angiotensinogen gene and interindividual variation in response to angiotensin-converting enzyme inhibitors |
title_fullStr |
A core promoter variant of angiotensinogen gene and interindividual variation in response to angiotensin-converting enzyme inhibitors |
title_full_unstemmed |
A core promoter variant of angiotensinogen gene and interindividual variation in response to angiotensin-converting enzyme inhibitors |
title_sort |
core promoter variant of angiotensinogen gene and interindividual variation in response to angiotensin-converting enzyme inhibitors |
publisher |
Hindawi - SAGE Publishing |
series |
Journal of the Renin-Angiotensin-Aldosterone System |
issn |
1470-3203 1752-8976 |
publishDate |
2014-12-01 |
description |
Introduction: The polymorphic angiotensinogen (AGT) gene is one of the most promising candidates for essential hypertension. The aim of this study was to examine the association between the A-6G variant of the AGT gene and the blood pressure response to angiotensin-converting enzyme (ACE) inhibitors in hypertensive subjects. Methods: Five hundred and nine mildly to moderately hypertensive subjects received ACE inhibitors for six weeks after a two-week run-in period. AGT genotyping was performed by direct polymerase chain reaction amplification and deoxyribonucleic acid (DNA) nucleotide sequencing from peripheral blood. Results: The AA genotype, AG genotype, and GG genotype were present in 301 (59.1%), 186 (36.6%), and 22 (4.3%) of patients, respectively. As compared with patients carrying the AA or AG genotype, those carrying the GG genotype had significantly greater reductions in systolic blood pressure, diastolic blood pressure, pulse pressure and mean arterial pressure ( p =0.007, 0.014, 0.027 and 0.005, respectively). Moreover, stepwise multiple linear regression analysis showed that the A-6G genotype was a significant predictor of systolic blood pressure and pulse pressure reductions ( p= 0.040 and 0.019, respectively). Conclusion: Our study indicates that the A-6G variant of the AGT gene may be an important determinant of interindividual variation in the response to ACE inhibitors. |
url |
https://doi.org/10.1177/1470320313506481 |
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