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Insertion/deletion polymorphism of the ACE gene increased risk of Behcet disease: evidence from a meta-analysis
BACKGROUND AND OBJECTIVES: Endothelial dysfunction has a role in the development of the Behcet disease (BD). Local renin–angiotensin system (RAS) plays a crucial role in the endothelial control, and angiotensin-converting enzyme (ACE) is the monitoring component of the RAS. We investigated the relat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
King Faisal Specialist Hospital and Research Centre
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074878/ https://www.ncbi.nlm.nih.gov/pubmed/24188936 http://dx.doi.org/10.5144/0256-4947.2013.437 |
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author | Mandal, Raju Kumar Yaday, Suraj Singh Panda, Aditya K. Khattri, Sanjay |
author_facet | Mandal, Raju Kumar Yaday, Suraj Singh Panda, Aditya K. Khattri, Sanjay |
author_sort | Mandal, Raju Kumar |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Endothelial dysfunction has a role in the development of the Behcet disease (BD). Local renin–angiotensin system (RAS) plays a crucial role in the endothelial control, and angiotensin-converting enzyme (ACE) is the monitoring component of the RAS. We investigated the relationship between the ACE Ins/Del (I/D) variants and the risk of BD. DESIGN AND SETTINGS: A meta-analysis was conducted from all published studies on the associations between the ACE I/D polymorphism and BD. METHODS: We systemically searched all published studies from PubMed and EMBASE, and data were quantitatively synthesized. Pooled odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated for allele, homozygous, heterozygous, and combined genetic models. RESULTS: Out of 5 eligible studies, 676 healthy controls and 534 BD cases were included in the present meta-analysis. D allele carrier was significantly associated with increased BD risk (D vs I: P=.002; OR=1.321, 95% CI=1.111–1.570). Homozygous mutant DD genotype also revealed 1.5-fold increased risk (DD vs II; P=.004; OR=1.573, 95% CI=1.156–2.141). In addition, the dominant genetic model demonstrated an increased risk of developing BD (DD vs II+ID: P=.001; OR=1.610, 95% CI=1.242–2.087) CONCLUSION: The current study suggests that ACE gene polymorphism (Ins/Del) contributes an increased susceptibility to BD. However, larger studies with stratified case control population and biological characterization are needed to validate this finding. |
format | Online Article Text |
id | pubmed-6074878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | King Faisal Specialist Hospital and Research Centre |
record_format | MEDLINE/PubMed |
spelling | pubmed-60748782018-09-21 Insertion/deletion polymorphism of the ACE gene increased risk of Behcet disease: evidence from a meta-analysis Mandal, Raju Kumar Yaday, Suraj Singh Panda, Aditya K. Khattri, Sanjay Ann Saudi Med Original Article BACKGROUND AND OBJECTIVES: Endothelial dysfunction has a role in the development of the Behcet disease (BD). Local renin–angiotensin system (RAS) plays a crucial role in the endothelial control, and angiotensin-converting enzyme (ACE) is the monitoring component of the RAS. We investigated the relationship between the ACE Ins/Del (I/D) variants and the risk of BD. DESIGN AND SETTINGS: A meta-analysis was conducted from all published studies on the associations between the ACE I/D polymorphism and BD. METHODS: We systemically searched all published studies from PubMed and EMBASE, and data were quantitatively synthesized. Pooled odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated for allele, homozygous, heterozygous, and combined genetic models. RESULTS: Out of 5 eligible studies, 676 healthy controls and 534 BD cases were included in the present meta-analysis. D allele carrier was significantly associated with increased BD risk (D vs I: P=.002; OR=1.321, 95% CI=1.111–1.570). Homozygous mutant DD genotype also revealed 1.5-fold increased risk (DD vs II; P=.004; OR=1.573, 95% CI=1.156–2.141). In addition, the dominant genetic model demonstrated an increased risk of developing BD (DD vs II+ID: P=.001; OR=1.610, 95% CI=1.242–2.087) CONCLUSION: The current study suggests that ACE gene polymorphism (Ins/Del) contributes an increased susceptibility to BD. However, larger studies with stratified case control population and biological characterization are needed to validate this finding. King Faisal Specialist Hospital and Research Centre 2013 /pmc/articles/PMC6074878/ /pubmed/24188936 http://dx.doi.org/10.5144/0256-4947.2013.437 Text en Copyright © 2013, Annals of Saudi Medicine This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Mandal, Raju Kumar Yaday, Suraj Singh Panda, Aditya K. Khattri, Sanjay Insertion/deletion polymorphism of the ACE gene increased risk of Behcet disease: evidence from a meta-analysis |
title | Insertion/deletion polymorphism of the ACE gene increased risk of Behcet disease: evidence from a meta-analysis |
title_full | Insertion/deletion polymorphism of the ACE gene increased risk of Behcet disease: evidence from a meta-analysis |
title_fullStr | Insertion/deletion polymorphism of the ACE gene increased risk of Behcet disease: evidence from a meta-analysis |
title_full_unstemmed | Insertion/deletion polymorphism of the ACE gene increased risk of Behcet disease: evidence from a meta-analysis |
title_short | Insertion/deletion polymorphism of the ACE gene increased risk of Behcet disease: evidence from a meta-analysis |
title_sort | insertion/deletion polymorphism of the ace gene increased risk of behcet disease: evidence from a meta-analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074878/ https://www.ncbi.nlm.nih.gov/pubmed/24188936 http://dx.doi.org/10.5144/0256-4947.2013.437 |
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