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LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography
BACKGROUND: Polymorphisms in the LPA gene were associated with coronary artery disease (CAD). However, there are differences in the allelic frequencies, Lp(a) levels, and significant association with CAD according to ethnic groups. In this scenario, the main aim of this study was to assess the influ...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108154/ https://www.ncbi.nlm.nih.gov/pubmed/24776095 http://dx.doi.org/10.1186/1476-511X-13-74 |
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author | Santos, Paulo CJL Bueno, Carolina T Lemos, Pedro A Krieger, José E Pereira, Alexandre C |
author_facet | Santos, Paulo CJL Bueno, Carolina T Lemos, Pedro A Krieger, José E Pereira, Alexandre C |
author_sort | Santos, Paulo CJL |
collection | PubMed |
description | BACKGROUND: Polymorphisms in the LPA gene were associated with coronary artery disease (CAD). However, there are differences in the allelic frequencies, Lp(a) levels, and significant association with CAD according to ethnic groups. In this scenario, the main aim of this study was to assess the influence of the LPA polymorphisms on coronary lesions in Brazilian patients. METHODS: 1,394 consecutive patients submitted to coronary angiography to study suggestive CAD and twenty coronary segments were scored. Genotyping for the LPA rs10455872 and rs3798220 polymorphisms were performed by high resolution melting analysis. RESULTS: The frequencies of the rs10455872 G and rs3798220 C variant alleles were 6.4% and 6.2%, respectively. LPA rs10455872 G variant allele was associated with higher odds ratio of having coronary lesions in an adjusted model (OR = 2.02, 95% CI = 1.10-3.72, p = 0.02). Scores of coronary lesions (extension, severity, and Gensini scores) were significantly different among rs10455872 genotype groups. Coronary lesions was not associated with LPA rs3798220 (OR = 1.09, 95% CI = 0.67-1.76, p = 0.73) and scores of coronary lesions were not different among rs3798220 genotypes. CONCLUSIONS: We confirmed the association of the LPA rs10455872 with CAD in a large sample of Brazilian patients. For the LPA rs3798220, our finding is consistent with studies which showed the lack of this genetic association. |
format | Online Article Text |
id | pubmed-4108154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41081542014-07-24 LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography Santos, Paulo CJL Bueno, Carolina T Lemos, Pedro A Krieger, José E Pereira, Alexandre C Lipids Health Dis Research BACKGROUND: Polymorphisms in the LPA gene were associated with coronary artery disease (CAD). However, there are differences in the allelic frequencies, Lp(a) levels, and significant association with CAD according to ethnic groups. In this scenario, the main aim of this study was to assess the influence of the LPA polymorphisms on coronary lesions in Brazilian patients. METHODS: 1,394 consecutive patients submitted to coronary angiography to study suggestive CAD and twenty coronary segments were scored. Genotyping for the LPA rs10455872 and rs3798220 polymorphisms were performed by high resolution melting analysis. RESULTS: The frequencies of the rs10455872 G and rs3798220 C variant alleles were 6.4% and 6.2%, respectively. LPA rs10455872 G variant allele was associated with higher odds ratio of having coronary lesions in an adjusted model (OR = 2.02, 95% CI = 1.10-3.72, p = 0.02). Scores of coronary lesions (extension, severity, and Gensini scores) were significantly different among rs10455872 genotype groups. Coronary lesions was not associated with LPA rs3798220 (OR = 1.09, 95% CI = 0.67-1.76, p = 0.73) and scores of coronary lesions were not different among rs3798220 genotypes. CONCLUSIONS: We confirmed the association of the LPA rs10455872 with CAD in a large sample of Brazilian patients. For the LPA rs3798220, our finding is consistent with studies which showed the lack of this genetic association. BioMed Central 2014-04-29 /pmc/articles/PMC4108154/ /pubmed/24776095 http://dx.doi.org/10.1186/1476-511X-13-74 Text en Copyright © 2014 Santos et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Santos, Paulo CJL Bueno, Carolina T Lemos, Pedro A Krieger, José E Pereira, Alexandre C LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography |
title | LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography |
title_full | LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography |
title_fullStr | LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography |
title_full_unstemmed | LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography |
title_short | LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography |
title_sort | lpa rs10455872 polymorphism is associated with coronary lesions in brazilian patients submitted to coronary angiography |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108154/ https://www.ncbi.nlm.nih.gov/pubmed/24776095 http://dx.doi.org/10.1186/1476-511X-13-74 |
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