Factor V Leiden mutation is not a predisposing factor for acute coronary syndromes

Background: The prevalence of Coronary artery disease (CAD) in India has increased considerably over the past few years and could become the number one killer disease if interventions are not done. Factor V Leiden (FVL) mutation and FII G20210A polymorphism are two recently described genetic factors...

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Main Authors: G. Himabindu, D. Rajasekhar, K. Latheef, P.V.G.K. Sarma, V. Vanajakshamma, Abhijit Chaudhury, Aparna R. Bitla
Format: Article
Language:English
Published: Elsevier 2012-11-01
Series:Indian Heart Journal
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0019483212000582
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spelling doaj-83d4f99d2e764d699d57686d3a3dc2072020-11-24T23:16:18ZengElsevierIndian Heart Journal0019-48322012-11-0164657057510.1016/j.ihj.2012.07.006Factor V Leiden mutation is not a predisposing factor for acute coronary syndromesG. Himabindu0D. Rajasekhar1K. Latheef2P.V.G.K. Sarma3V. Vanajakshamma4Abhijit Chaudhury5Aparna R. Bitla6Department of Cardiology, Sri Venkateswara Institute of Medical Sciences & University, Tirupati 517507, Andhra Pradesh, IndiaDepartment of Cardiology, Sri Venkateswara Institute of Medical Sciences & University, Tirupati 517507, Andhra Pradesh, IndiaDepartment of Cardiology, Sri Venkateswara Institute of Medical Sciences & University, Tirupati 517507, Andhra Pradesh, IndiaDepartment of Biotechnology, Sri Venkateswara Institute of Medical Sciences & University, Tirupati, Andhra Pradesh, IndiaDepartment of Cardiology, Sri Venkateswara Institute of Medical Sciences & University, Tirupati 517507, Andhra Pradesh, IndiaDepartment of Microbiology, Sri Venkateswara Institute of Medical Sciences & University, Tirupati, Andhra Pradesh, IndiaDepartment of Biochemistry, Sri Venkateswara Institute of Medical Sciences & University, Tirupati, Andhra Pradesh, IndiaBackground: The prevalence of Coronary artery disease (CAD) in India has increased considerably over the past few years and could become the number one killer disease if interventions are not done. Factor V Leiden (FVL) mutation and FII G20210A polymorphism are two recently described genetic factors with a propensity towards venous thrombosis. This warrants the investigations for thrombophilia in myocardial infarction patients in India. Methods: The study cohort consisted of 51 patients aged below 50 years presenting with acute coronary syndromes. In both patient group and normal individuals the major risk factors Protein C deficiency, Protein S deficiency, anticardiolipin antibodies, Fibrinogen and Lipoprotein [a] were studied. Factor V Leiden (FVL) G1691A mutation in both control and patient group was looked by using Polymerase chain reaction (PCR) followed by sequencing of the PCR products. Results: Our results indicated significantly higher levels of anticardiolipin antibodies and fibrinogen in the patients and absence of FVL (G1691A) mutation in our study cohort. One of the patients (H5) showed insertion of an extra A nucleotide in exon 10 of the Factor V gene resulting in frame shift mutation in this patient. Conclusion: The results of present study showed absence of FVL mutation in our population. However, there is a need to confirm the above findings on patients from different populations from different parts of the country. The insertion of an extra A in exon 10 in the patient needs to be ascertained to confirm that it is one of its kinds or is prevalent in the population.http://www.sciencedirect.com/science/article/pii/S0019483212000582Coronary artery diseaseFactor V Leiden mutationPolymerase chain reaction
collection DOAJ
language English
format Article
sources DOAJ
author G. Himabindu
D. Rajasekhar
K. Latheef
P.V.G.K. Sarma
V. Vanajakshamma
Abhijit Chaudhury
Aparna R. Bitla
spellingShingle G. Himabindu
D. Rajasekhar
K. Latheef
P.V.G.K. Sarma
V. Vanajakshamma
Abhijit Chaudhury
Aparna R. Bitla
Factor V Leiden mutation is not a predisposing factor for acute coronary syndromes
Indian Heart Journal
Coronary artery disease
Factor V Leiden mutation
Polymerase chain reaction
author_facet G. Himabindu
D. Rajasekhar
K. Latheef
P.V.G.K. Sarma
V. Vanajakshamma
Abhijit Chaudhury
Aparna R. Bitla
author_sort G. Himabindu
title Factor V Leiden mutation is not a predisposing factor for acute coronary syndromes
title_short Factor V Leiden mutation is not a predisposing factor for acute coronary syndromes
title_full Factor V Leiden mutation is not a predisposing factor for acute coronary syndromes
title_fullStr Factor V Leiden mutation is not a predisposing factor for acute coronary syndromes
title_full_unstemmed Factor V Leiden mutation is not a predisposing factor for acute coronary syndromes
title_sort factor v leiden mutation is not a predisposing factor for acute coronary syndromes
publisher Elsevier
series Indian Heart Journal
issn 0019-4832
publishDate 2012-11-01
description Background: The prevalence of Coronary artery disease (CAD) in India has increased considerably over the past few years and could become the number one killer disease if interventions are not done. Factor V Leiden (FVL) mutation and FII G20210A polymorphism are two recently described genetic factors with a propensity towards venous thrombosis. This warrants the investigations for thrombophilia in myocardial infarction patients in India. Methods: The study cohort consisted of 51 patients aged below 50 years presenting with acute coronary syndromes. In both patient group and normal individuals the major risk factors Protein C deficiency, Protein S deficiency, anticardiolipin antibodies, Fibrinogen and Lipoprotein [a] were studied. Factor V Leiden (FVL) G1691A mutation in both control and patient group was looked by using Polymerase chain reaction (PCR) followed by sequencing of the PCR products. Results: Our results indicated significantly higher levels of anticardiolipin antibodies and fibrinogen in the patients and absence of FVL (G1691A) mutation in our study cohort. One of the patients (H5) showed insertion of an extra A nucleotide in exon 10 of the Factor V gene resulting in frame shift mutation in this patient. Conclusion: The results of present study showed absence of FVL mutation in our population. However, there is a need to confirm the above findings on patients from different populations from different parts of the country. The insertion of an extra A in exon 10 in the patient needs to be ascertained to confirm that it is one of its kinds or is prevalent in the population.
topic Coronary artery disease
Factor V Leiden mutation
Polymerase chain reaction
url http://www.sciencedirect.com/science/article/pii/S0019483212000582
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