Alu insertion/deletion of ACE gene polymorphism might not affect significantly the serum bradykinin level in hypertensive patients taking ACE inhibitors

Background: Angiotensin I-converting enzyme (ACE) has two homologous catalytic domains, the N- and C-domains. Our previous study suggested that Alu insertion (I allele) in the intron 16 of ACE resulted in premature codon termination. The I allele has only one active site in the N-domain while the Al...

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Main Authors: Widodo, Shila Wisnasari, Mohammad Saifur Rohman, Lowry Yunita, Mifetika Lukitasari, Maulidiyatun Nuril, Kholifah Holil, Dian Laila Purwaningroom
Format: Article
Language:English
Published: SpringerOpen 2017-04-01
Series:Egyptian Journal of Medical Human Genetics
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1110863016300519
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spelling doaj-50122df1909147098963255c5f312a722020-11-25T02:29:51ZengSpringerOpenEgyptian Journal of Medical Human Genetics1110-86302017-04-0118218719110.1016/j.ejmhg.2016.08.001Alu insertion/deletion of ACE gene polymorphism might not affect significantly the serum bradykinin level in hypertensive patients taking ACE inhibitorsWidodo0Shila Wisnasari1Mohammad Saifur Rohman2Lowry Yunita3Mifetika Lukitasari4Maulidiyatun Nuril5Kholifah Holil6Dian Laila Purwaningroom7Biology Department, Faculty of Mathematics and Natural Sciences, Brawijaya University, Malang, IndonesiaBiomedical Science, Faculty of Medicine, Brawijaya University, Malang, IndonesiaDepartment of Cardiology and Vascular Medicine, Faculty of Medicine, Brawijaya University and Saiful Anwar General Hospital, Malang, IndonesiaDepartment of Cardiology and Vascular Medicine, Faculty of Medicine, Brawijaya University and Saiful Anwar General Hospital, Malang, IndonesiaNursing Science, Faculty of Medicine, Brawijaya University, Malang, IndonesiaBiology Department, Faculty of Science and Technology, Islamic State University of Maulana Malik Ibrahim, Malang, IndonesiaBiology Department, Faculty of Science and Technology, Islamic State University of Maulana Malik Ibrahim, Malang, IndonesiaFaculty of Health Science, Muhammadiyah University, Ponorogo, IndonesiaBackground: Angiotensin I-converting enzyme (ACE) has two homologous catalytic domains, the N- and C-domains. Our previous study suggested that Alu insertion (I allele) in the intron 16 of ACE resulted in premature codon termination. The I allele has only one active site in the N-domain while the Alu deletion (D allele) still has two active sites of ACE. Therefore the effect of I/D polymorphism of ACE on the enzyme’s ability to catalyse bradykinin is still not widely known. Aims: This study aimed to examine the serum bradykinin level in hypertensive patients with I/D polymorphism of ACE, who were treated with ACE inhibitor. Subjects and methods: The serum bradykinin and I/D polymorphism have been detected in 64 hypertensive patients taking ACE inhibitor (lisinopril or captopril) for at least eight weeks with good medication adherence. The binding affinity of ACE with its receptor was calculated by molecular docking. Results: The findings show that genotype II is more frequent in the population the researchers observed (53.12%) compared to ID (23.44%) and DD (23.44%) variances. On the other hand, the bradykinin level is not affected by genotype of the ACE genes on the population. Bradykinin increases in patients with genotype II who are given captopril, but decreases in patients treated with lisinopril. Nevertheless, there is no statistically significant difference. Conclusion: This study suggests that the polymorphism might not significantly affect the serum bradykinin level in hypertensive patients taking ACE inhibitors.http://www.sciencedirect.com/science/article/pii/S1110863016300519Binding affinityAngiotensinBradykininI/D variant ACEACE inhibitor
collection DOAJ
language English
format Article
sources DOAJ
author Widodo
Shila Wisnasari
Mohammad Saifur Rohman
Lowry Yunita
Mifetika Lukitasari
Maulidiyatun Nuril
Kholifah Holil
Dian Laila Purwaningroom
spellingShingle Widodo
Shila Wisnasari
Mohammad Saifur Rohman
Lowry Yunita
Mifetika Lukitasari
Maulidiyatun Nuril
Kholifah Holil
Dian Laila Purwaningroom
Alu insertion/deletion of ACE gene polymorphism might not affect significantly the serum bradykinin level in hypertensive patients taking ACE inhibitors
Egyptian Journal of Medical Human Genetics
Binding affinity
Angiotensin
Bradykinin
I/D variant ACE
ACE inhibitor
author_facet Widodo
Shila Wisnasari
Mohammad Saifur Rohman
Lowry Yunita
Mifetika Lukitasari
Maulidiyatun Nuril
Kholifah Holil
Dian Laila Purwaningroom
author_sort Widodo
title Alu insertion/deletion of ACE gene polymorphism might not affect significantly the serum bradykinin level in hypertensive patients taking ACE inhibitors
title_short Alu insertion/deletion of ACE gene polymorphism might not affect significantly the serum bradykinin level in hypertensive patients taking ACE inhibitors
title_full Alu insertion/deletion of ACE gene polymorphism might not affect significantly the serum bradykinin level in hypertensive patients taking ACE inhibitors
title_fullStr Alu insertion/deletion of ACE gene polymorphism might not affect significantly the serum bradykinin level in hypertensive patients taking ACE inhibitors
title_full_unstemmed Alu insertion/deletion of ACE gene polymorphism might not affect significantly the serum bradykinin level in hypertensive patients taking ACE inhibitors
title_sort alu insertion/deletion of ace gene polymorphism might not affect significantly the serum bradykinin level in hypertensive patients taking ace inhibitors
publisher SpringerOpen
series Egyptian Journal of Medical Human Genetics
issn 1110-8630
publishDate 2017-04-01
description Background: Angiotensin I-converting enzyme (ACE) has two homologous catalytic domains, the N- and C-domains. Our previous study suggested that Alu insertion (I allele) in the intron 16 of ACE resulted in premature codon termination. The I allele has only one active site in the N-domain while the Alu deletion (D allele) still has two active sites of ACE. Therefore the effect of I/D polymorphism of ACE on the enzyme’s ability to catalyse bradykinin is still not widely known. Aims: This study aimed to examine the serum bradykinin level in hypertensive patients with I/D polymorphism of ACE, who were treated with ACE inhibitor. Subjects and methods: The serum bradykinin and I/D polymorphism have been detected in 64 hypertensive patients taking ACE inhibitor (lisinopril or captopril) for at least eight weeks with good medication adherence. The binding affinity of ACE with its receptor was calculated by molecular docking. Results: The findings show that genotype II is more frequent in the population the researchers observed (53.12%) compared to ID (23.44%) and DD (23.44%) variances. On the other hand, the bradykinin level is not affected by genotype of the ACE genes on the population. Bradykinin increases in patients with genotype II who are given captopril, but decreases in patients treated with lisinopril. Nevertheless, there is no statistically significant difference. Conclusion: This study suggests that the polymorphism might not significantly affect the serum bradykinin level in hypertensive patients taking ACE inhibitors.
topic Binding affinity
Angiotensin
Bradykinin
I/D variant ACE
ACE inhibitor
url http://www.sciencedirect.com/science/article/pii/S1110863016300519
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