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Matrix Metalloproteinase-1 Gene Polymorphism Associated with Ultrasound-Assessed Carotid Thickness among Older Adults

BACKGROUND AND AIM: Due to the high incidence of vascular diseases, it is necessary to identify new circulating or structural markers for predicting risk for chronic diseases. Some studies suggest that MMP1 gene polymorphisms are associated with the enzyme expression levels in situ (e.g., in atheros...

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Autores principales: Morais Junior, Gilberto Santos, Rodrigues, Nathalia Oliveira, Henriques, Adriane Dallanora, Tonet-Furioso, Audrey Cecília, Brito, Ciro José, Gomes, Lucy Oliveira, Moraes, Clayton Franco, Nóbrega, Otávio Toledo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033251/
https://www.ncbi.nlm.nih.gov/pubmed/30034880
http://dx.doi.org/10.1155/2018/1475890
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author Morais Junior, Gilberto Santos
Rodrigues, Nathalia Oliveira
Henriques, Adriane Dallanora
Tonet-Furioso, Audrey Cecília
Brito, Ciro José
Gomes, Lucy Oliveira
Moraes, Clayton Franco
Nóbrega, Otávio Toledo
author_facet Morais Junior, Gilberto Santos
Rodrigues, Nathalia Oliveira
Henriques, Adriane Dallanora
Tonet-Furioso, Audrey Cecília
Brito, Ciro José
Gomes, Lucy Oliveira
Moraes, Clayton Franco
Nóbrega, Otávio Toledo
author_sort Morais Junior, Gilberto Santos
collection PubMed
description BACKGROUND AND AIM: Due to the high incidence of vascular diseases, it is necessary to identify new circulating or structural markers for predicting risk for chronic diseases. Some studies suggest that MMP1 gene polymorphisms are associated with the enzyme expression levels in situ (e.g., in atherosclerotic plaques). OBJECTIVES: Thus, the study of this polymorphism may help understanding the pathophysiology of coronary disease. METHODS: We performed cross-sectional clinical and laboratory evaluations (including measurement of intima-media thickness of carotid arteries) and genotyping of the MMP1 SNP rs495366 (A/G) in 366 elderly people. RESULTS: No significant differences between genotypes were noted for biochemical, metabolic, inflammatory, or clinical variables except for a significant difference in intima-media thickness for the left carotid artery and a trend toward significance for the right counterpart. CONCLUSION: Carriers of the allele associated with lower MMP1 expression (allele A) presented greater carotid thickness. We suggest that the phenomenon can be explained by impaired remodeling of the arterial wall (poor degradation of collagen fibers in this scenario), yielding carotid wall thickening and a greater intrinsic risk for cerebrovascular events.
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spelling pubmed-60332512018-07-22 Matrix Metalloproteinase-1 Gene Polymorphism Associated with Ultrasound-Assessed Carotid Thickness among Older Adults Morais Junior, Gilberto Santos Rodrigues, Nathalia Oliveira Henriques, Adriane Dallanora Tonet-Furioso, Audrey Cecília Brito, Ciro José Gomes, Lucy Oliveira Moraes, Clayton Franco Nóbrega, Otávio Toledo J Aging Res Research Article BACKGROUND AND AIM: Due to the high incidence of vascular diseases, it is necessary to identify new circulating or structural markers for predicting risk for chronic diseases. Some studies suggest that MMP1 gene polymorphisms are associated with the enzyme expression levels in situ (e.g., in atherosclerotic plaques). OBJECTIVES: Thus, the study of this polymorphism may help understanding the pathophysiology of coronary disease. METHODS: We performed cross-sectional clinical and laboratory evaluations (including measurement of intima-media thickness of carotid arteries) and genotyping of the MMP1 SNP rs495366 (A/G) in 366 elderly people. RESULTS: No significant differences between genotypes were noted for biochemical, metabolic, inflammatory, or clinical variables except for a significant difference in intima-media thickness for the left carotid artery and a trend toward significance for the right counterpart. CONCLUSION: Carriers of the allele associated with lower MMP1 expression (allele A) presented greater carotid thickness. We suggest that the phenomenon can be explained by impaired remodeling of the arterial wall (poor degradation of collagen fibers in this scenario), yielding carotid wall thickening and a greater intrinsic risk for cerebrovascular events. Hindawi 2018-06-21 /pmc/articles/PMC6033251/ /pubmed/30034880 http://dx.doi.org/10.1155/2018/1475890 Text en Copyright © 2018 Gilberto Santos Morais Junior et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Morais Junior, Gilberto Santos
Rodrigues, Nathalia Oliveira
Henriques, Adriane Dallanora
Tonet-Furioso, Audrey Cecília
Brito, Ciro José
Gomes, Lucy Oliveira
Moraes, Clayton Franco
Nóbrega, Otávio Toledo
Matrix Metalloproteinase-1 Gene Polymorphism Associated with Ultrasound-Assessed Carotid Thickness among Older Adults
title Matrix Metalloproteinase-1 Gene Polymorphism Associated with Ultrasound-Assessed Carotid Thickness among Older Adults
title_full Matrix Metalloproteinase-1 Gene Polymorphism Associated with Ultrasound-Assessed Carotid Thickness among Older Adults
title_fullStr Matrix Metalloproteinase-1 Gene Polymorphism Associated with Ultrasound-Assessed Carotid Thickness among Older Adults
title_full_unstemmed Matrix Metalloproteinase-1 Gene Polymorphism Associated with Ultrasound-Assessed Carotid Thickness among Older Adults
title_short Matrix Metalloproteinase-1 Gene Polymorphism Associated with Ultrasound-Assessed Carotid Thickness among Older Adults
title_sort matrix metalloproteinase-1 gene polymorphism associated with ultrasound-assessed carotid thickness among older adults
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033251/
https://www.ncbi.nlm.nih.gov/pubmed/30034880
http://dx.doi.org/10.1155/2018/1475890
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