Cargando…

Association study of matrix metalloproteinase 3 5A/6A polymorphism with in-stent restenosis after percutaneous coronary interventions in a Han Chinese population

OBJECTIVE: We aimed to investigate the association between the 5A/6A promoter polymorphism in the matrix metalloproteinase 3 (MMP3) gene and in-stent restenosis (ISR) in a regional Chinese population. METHODS: A total of 818 patients who underwent primary implantation of drug-eluting stents were enr...

Descripción completa

Detalles Bibliográficos
Autores principales: Du, Ji-Bing, Zhang, Wei, Li, Na, Jiang, Hua, Liu, Yin, Gao, Jing, Chen, Shu-Tao, Cong, Hong-Liang, Wei, Yi-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140217/
https://www.ncbi.nlm.nih.gov/pubmed/30732526
http://dx.doi.org/10.1177/0300060519827145
_version_ 1783518944780353536
author Du, Ji-Bing
Zhang, Wei
Li, Na
Jiang, Hua
Liu, Yin
Gao, Jing
Chen, Shu-Tao
Cong, Hong-Liang
Wei, Yi-Liang
author_facet Du, Ji-Bing
Zhang, Wei
Li, Na
Jiang, Hua
Liu, Yin
Gao, Jing
Chen, Shu-Tao
Cong, Hong-Liang
Wei, Yi-Liang
author_sort Du, Ji-Bing
collection PubMed
description OBJECTIVE: We aimed to investigate the association between the 5A/6A promoter polymorphism in the matrix metalloproteinase 3 (MMP3) gene and in-stent restenosis (ISR) in a regional Chinese population. METHODS: A total of 818 patients who underwent primary implantation of drug-eluting stents were enrolled and received a 6-month follow-up angiography and DNA genotyping of the 5A/6A polymorphism. RESULTS: ISR was found in 36.9% of all patients (302 ISR vs. 516 no ISR). The genotype proportion of 6A6A was significantly increased in ISRs (74.2% ISR vs. 66.8% no ISR), whereas the allele frequency of 5A was significantly decreased in ISR patients (25.8%) compared with controls who did not undergo ISR (33.1%). CONCLUSIONS: Our data indicate that the MMP3 6A6A genotype is a genetic susceptibility factor for ISR after coronary stent placement, but the 5A allele can lower the risk for patients within 6 months after stenting. Therefore, genotyping 5A/6A in the MMP3 promoter is suggested for patients who undergo coronary stent implantation.
format Online
Article
Text
id pubmed-7140217
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-71402172020-04-13 Association study of matrix metalloproteinase 3 5A/6A polymorphism with in-stent restenosis after percutaneous coronary interventions in a Han Chinese population Du, Ji-Bing Zhang, Wei Li, Na Jiang, Hua Liu, Yin Gao, Jing Chen, Shu-Tao Cong, Hong-Liang Wei, Yi-Liang J Int Med Res Special Issue: Prevention and Treatment of Cardiovascular Disease OBJECTIVE: We aimed to investigate the association between the 5A/6A promoter polymorphism in the matrix metalloproteinase 3 (MMP3) gene and in-stent restenosis (ISR) in a regional Chinese population. METHODS: A total of 818 patients who underwent primary implantation of drug-eluting stents were enrolled and received a 6-month follow-up angiography and DNA genotyping of the 5A/6A polymorphism. RESULTS: ISR was found in 36.9% of all patients (302 ISR vs. 516 no ISR). The genotype proportion of 6A6A was significantly increased in ISRs (74.2% ISR vs. 66.8% no ISR), whereas the allele frequency of 5A was significantly decreased in ISR patients (25.8%) compared with controls who did not undergo ISR (33.1%). CONCLUSIONS: Our data indicate that the MMP3 6A6A genotype is a genetic susceptibility factor for ISR after coronary stent placement, but the 5A allele can lower the risk for patients within 6 months after stenting. Therefore, genotyping 5A/6A in the MMP3 promoter is suggested for patients who undergo coronary stent implantation. SAGE Publications 2019-02-08 /pmc/articles/PMC7140217/ /pubmed/30732526 http://dx.doi.org/10.1177/0300060519827145 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Special Issue: Prevention and Treatment of Cardiovascular Disease
Du, Ji-Bing
Zhang, Wei
Li, Na
Jiang, Hua
Liu, Yin
Gao, Jing
Chen, Shu-Tao
Cong, Hong-Liang
Wei, Yi-Liang
Association study of matrix metalloproteinase 3 5A/6A polymorphism with in-stent restenosis after percutaneous coronary interventions in a Han Chinese population
title Association study of matrix metalloproteinase 3 5A/6A polymorphism with in-stent restenosis after percutaneous coronary interventions in a Han Chinese population
title_full Association study of matrix metalloproteinase 3 5A/6A polymorphism with in-stent restenosis after percutaneous coronary interventions in a Han Chinese population
title_fullStr Association study of matrix metalloproteinase 3 5A/6A polymorphism with in-stent restenosis after percutaneous coronary interventions in a Han Chinese population
title_full_unstemmed Association study of matrix metalloproteinase 3 5A/6A polymorphism with in-stent restenosis after percutaneous coronary interventions in a Han Chinese population
title_short Association study of matrix metalloproteinase 3 5A/6A polymorphism with in-stent restenosis after percutaneous coronary interventions in a Han Chinese population
title_sort association study of matrix metalloproteinase 3 5a/6a polymorphism with in-stent restenosis after percutaneous coronary interventions in a han chinese population
topic Special Issue: Prevention and Treatment of Cardiovascular Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140217/
https://www.ncbi.nlm.nih.gov/pubmed/30732526
http://dx.doi.org/10.1177/0300060519827145
work_keys_str_mv AT dujibing associationstudyofmatrixmetalloproteinase35a6apolymorphismwithinstentrestenosisafterpercutaneouscoronaryinterventionsinahanchinesepopulation
AT zhangwei associationstudyofmatrixmetalloproteinase35a6apolymorphismwithinstentrestenosisafterpercutaneouscoronaryinterventionsinahanchinesepopulation
AT lina associationstudyofmatrixmetalloproteinase35a6apolymorphismwithinstentrestenosisafterpercutaneouscoronaryinterventionsinahanchinesepopulation
AT jianghua associationstudyofmatrixmetalloproteinase35a6apolymorphismwithinstentrestenosisafterpercutaneouscoronaryinterventionsinahanchinesepopulation
AT liuyin associationstudyofmatrixmetalloproteinase35a6apolymorphismwithinstentrestenosisafterpercutaneouscoronaryinterventionsinahanchinesepopulation
AT gaojing associationstudyofmatrixmetalloproteinase35a6apolymorphismwithinstentrestenosisafterpercutaneouscoronaryinterventionsinahanchinesepopulation
AT chenshutao associationstudyofmatrixmetalloproteinase35a6apolymorphismwithinstentrestenosisafterpercutaneouscoronaryinterventionsinahanchinesepopulation
AT conghongliang associationstudyofmatrixmetalloproteinase35a6apolymorphismwithinstentrestenosisafterpercutaneouscoronaryinterventionsinahanchinesepopulation
AT weiyiliang associationstudyofmatrixmetalloproteinase35a6apolymorphismwithinstentrestenosisafterpercutaneouscoronaryinterventionsinahanchinesepopulation