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Insertion/deletion polymorphism of ACE gene in females with peripartum cardiomyopathy: A case-control study

BACKGROUND: The role of polymorphism of Angiotensin converting enzyme (ACE) gene and ACE activity in etiopathogenesis, prognosis, and many other clinical parameters in the various form of the cardiovascular disease has been established to some degree of certainty. The pathophysiology of Peripartum c...

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Autores principales: Yaqoob, Irfan, Tramboo, Nisar A., Bhat, Irfan A., Pandith, Arshad, Beig, Jahangir R., Hafeez, Imran, Lone, Aijaz A., Shah, Tariq R., Samreen, Sumera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902816/
https://www.ncbi.nlm.nih.gov/pubmed/29455790
http://dx.doi.org/10.1016/j.ihj.2017.05.020
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author Yaqoob, Irfan
Tramboo, Nisar A.
Bhat, Irfan A.
Pandith, Arshad
Beig, Jahangir R.
Hafeez, Imran
Lone, Aijaz A.
Shah, Tariq R.
Samreen, Sumera
author_facet Yaqoob, Irfan
Tramboo, Nisar A.
Bhat, Irfan A.
Pandith, Arshad
Beig, Jahangir R.
Hafeez, Imran
Lone, Aijaz A.
Shah, Tariq R.
Samreen, Sumera
author_sort Yaqoob, Irfan
collection PubMed
description BACKGROUND: The role of polymorphism of Angiotensin converting enzyme (ACE) gene and ACE activity in etiopathogenesis, prognosis, and many other clinical parameters in the various form of the cardiovascular disease has been established to some degree of certainty. The pathophysiology of Peripartum cardiomyopathy (PPCM) remains an area of active research. The main aim of our study was to see pattern of ACE- Insertion/Deletion (I/D) allele in PPCM and its implications on left ventricular performance indices. METHODS: This single-center case-control study included 45 cases and 70 controls. The diagnosis of PPCM was established clinically and echocardiographically. ACE genotyping was done by polymerase chain reaction (PCR) method in all subjects. RESULTS: The II, ID, and DD genotype was present in 16, 18 and 11 of subjects with PPCM and 48, 19 and 3 of controls respectively. The odds ratio for ACE-II genotype in cases vs. controls was 0.253 (95% CI = 0.114–0.558; p = 0.007), for that of II genotype was 1.93 (95% CI = 0.86–4.3; p = 0.107) and for DD genotype was 7.225 (95% CI; 1.88–27.6; p = 0.0039). Overall frequency of D allele in cases was significantly higher than controls (odds = 4.25; 95% CI = 2.01–6.7; p = 0.0001). Moreover, ejection fraction, left ventricular volume and linear dimensions were worse in patients with DD genotype. CONCLUSION: ACE DD genotype and overall frequency of D allele is significantly higher in patients with PPCM. Also, the presence of DD genotype is associated with worse systolic performance indices measured echocardiographically.
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spelling pubmed-59028162019-01-01 Insertion/deletion polymorphism of ACE gene in females with peripartum cardiomyopathy: A case-control study Yaqoob, Irfan Tramboo, Nisar A. Bhat, Irfan A. Pandith, Arshad Beig, Jahangir R. Hafeez, Imran Lone, Aijaz A. Shah, Tariq R. Samreen, Sumera Indian Heart J Original Article BACKGROUND: The role of polymorphism of Angiotensin converting enzyme (ACE) gene and ACE activity in etiopathogenesis, prognosis, and many other clinical parameters in the various form of the cardiovascular disease has been established to some degree of certainty. The pathophysiology of Peripartum cardiomyopathy (PPCM) remains an area of active research. The main aim of our study was to see pattern of ACE- Insertion/Deletion (I/D) allele in PPCM and its implications on left ventricular performance indices. METHODS: This single-center case-control study included 45 cases and 70 controls. The diagnosis of PPCM was established clinically and echocardiographically. ACE genotyping was done by polymerase chain reaction (PCR) method in all subjects. RESULTS: The II, ID, and DD genotype was present in 16, 18 and 11 of subjects with PPCM and 48, 19 and 3 of controls respectively. The odds ratio for ACE-II genotype in cases vs. controls was 0.253 (95% CI = 0.114–0.558; p = 0.007), for that of II genotype was 1.93 (95% CI = 0.86–4.3; p = 0.107) and for DD genotype was 7.225 (95% CI; 1.88–27.6; p = 0.0039). Overall frequency of D allele in cases was significantly higher than controls (odds = 4.25; 95% CI = 2.01–6.7; p = 0.0001). Moreover, ejection fraction, left ventricular volume and linear dimensions were worse in patients with DD genotype. CONCLUSION: ACE DD genotype and overall frequency of D allele is significantly higher in patients with PPCM. Also, the presence of DD genotype is associated with worse systolic performance indices measured echocardiographically. Elsevier 2018 2017-06-01 /pmc/articles/PMC5902816/ /pubmed/29455790 http://dx.doi.org/10.1016/j.ihj.2017.05.020 Text en © 2017 Published by Elsevier B.V. on behalf of Cardiological Society of India. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Yaqoob, Irfan
Tramboo, Nisar A.
Bhat, Irfan A.
Pandith, Arshad
Beig, Jahangir R.
Hafeez, Imran
Lone, Aijaz A.
Shah, Tariq R.
Samreen, Sumera
Insertion/deletion polymorphism of ACE gene in females with peripartum cardiomyopathy: A case-control study
title Insertion/deletion polymorphism of ACE gene in females with peripartum cardiomyopathy: A case-control study
title_full Insertion/deletion polymorphism of ACE gene in females with peripartum cardiomyopathy: A case-control study
title_fullStr Insertion/deletion polymorphism of ACE gene in females with peripartum cardiomyopathy: A case-control study
title_full_unstemmed Insertion/deletion polymorphism of ACE gene in females with peripartum cardiomyopathy: A case-control study
title_short Insertion/deletion polymorphism of ACE gene in females with peripartum cardiomyopathy: A case-control study
title_sort insertion/deletion polymorphism of ace gene in females with peripartum cardiomyopathy: a case-control study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902816/
https://www.ncbi.nlm.nih.gov/pubmed/29455790
http://dx.doi.org/10.1016/j.ihj.2017.05.020
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