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Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population
BACKGROUND: The study of the association between genotype and phenotype is of great importance for the prediction of multiple diseases and pathophysiological conditions. The relationship between angiotensin converting enzyme (ACE) Insertion/Deletion (I/D) polymorphism and Familial Hypercholesterolem...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220775/ https://www.ncbi.nlm.nih.gov/pubmed/24289455 http://dx.doi.org/10.1186/1476-511X-12-177 |
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author | Alharbi, Khalid K Kashour, Tarek S Al-Hussaini, Wejdan Al-Nbaheen, May Salem Mohamed, Sarar Hasanato, Rana MW Tamimi, Waleed Al-Naami, Mohammed Yahya Khan, Imran Ali |
author_facet | Alharbi, Khalid K Kashour, Tarek S Al-Hussaini, Wejdan Al-Nbaheen, May Salem Mohamed, Sarar Hasanato, Rana MW Tamimi, Waleed Al-Naami, Mohammed Yahya Khan, Imran Ali |
author_sort | Alharbi, Khalid K |
collection | PubMed |
description | BACKGROUND: The study of the association between genotype and phenotype is of great importance for the prediction of multiple diseases and pathophysiological conditions. The relationship between angiotensin converting enzyme (ACE) Insertion/Deletion (I/D) polymorphism and Familial Hypercholesterolemia (FH) has been not fully investigated in all the ethnicities. In this study we sought to determine the frequency of I/D polymorphism genotypes of ACE gene in Saudi patients with FH. RESULTS: This is a case–control study carried out purely in Saudi population. Genomic DNA was isolated from 128 subjects who have participated in this study. ACE gene I/D polymorphism was analyzed by polymerase chain reaction in 64 FH cases and 64 healthy controls. There was no statistically significant difference between the groups with respect to genotype distribution. Furthermore, we did not find any significant difference in the frequency of ACE I/D polymorphism in FH subjects when stratified by gender (p = 0.43). CONCLUSION: Our data suggest that ACE gene I/D polymorphism examined in this study has no role in predicting the occurrence and diagnosis of FH. |
format | Online Article Text |
id | pubmed-4220775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42207752014-11-06 Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population Alharbi, Khalid K Kashour, Tarek S Al-Hussaini, Wejdan Al-Nbaheen, May Salem Mohamed, Sarar Hasanato, Rana MW Tamimi, Waleed Al-Naami, Mohammed Yahya Khan, Imran Ali Lipids Health Dis Research BACKGROUND: The study of the association between genotype and phenotype is of great importance for the prediction of multiple diseases and pathophysiological conditions. The relationship between angiotensin converting enzyme (ACE) Insertion/Deletion (I/D) polymorphism and Familial Hypercholesterolemia (FH) has been not fully investigated in all the ethnicities. In this study we sought to determine the frequency of I/D polymorphism genotypes of ACE gene in Saudi patients with FH. RESULTS: This is a case–control study carried out purely in Saudi population. Genomic DNA was isolated from 128 subjects who have participated in this study. ACE gene I/D polymorphism was analyzed by polymerase chain reaction in 64 FH cases and 64 healthy controls. There was no statistically significant difference between the groups with respect to genotype distribution. Furthermore, we did not find any significant difference in the frequency of ACE I/D polymorphism in FH subjects when stratified by gender (p = 0.43). CONCLUSION: Our data suggest that ACE gene I/D polymorphism examined in this study has no role in predicting the occurrence and diagnosis of FH. BioMed Central 2013-12-01 /pmc/articles/PMC4220775/ /pubmed/24289455 http://dx.doi.org/10.1186/1476-511X-12-177 Text en Copyright © 2013 Alharbi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Alharbi, Khalid K Kashour, Tarek S Al-Hussaini, Wejdan Al-Nbaheen, May Salem Mohamed, Sarar Hasanato, Rana MW Tamimi, Waleed Al-Naami, Mohammed Yahya Khan, Imran Ali Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population |
title | Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population |
title_full | Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population |
title_fullStr | Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population |
title_full_unstemmed | Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population |
title_short | Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population |
title_sort | association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the saudi population |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220775/ https://www.ncbi.nlm.nih.gov/pubmed/24289455 http://dx.doi.org/10.1186/1476-511X-12-177 |
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