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Combined Effects of MMP-7, MMP-8 and MMP-26 on the Risk of Ischemic Stroke
Ischemic stroke (IS) is multifactorial causation combining with traditional cardiovascular disease (CVD) and genetic risk factors. Combined effects of MMP-7, MMP-8 and MMP-26 on the risk of IS remain incompletely understood. We aimed to assess individual and joint effects for IS risk by weighted gen...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912324/ https://www.ncbi.nlm.nih.gov/pubmed/31752174 http://dx.doi.org/10.3390/jcm8112011 |
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author | Hsieh, Fang-I Chiou, Hung-Yi Hu, Chaur-Jong Jeng, Jiann-Shing Lin, Huey-Juan Lee, Jiunn-Tay Lien, Li-Ming |
author_facet | Hsieh, Fang-I Chiou, Hung-Yi Hu, Chaur-Jong Jeng, Jiann-Shing Lin, Huey-Juan Lee, Jiunn-Tay Lien, Li-Ming |
author_sort | Hsieh, Fang-I |
collection | PubMed |
description | Ischemic stroke (IS) is multifactorial causation combining with traditional cardiovascular disease (CVD) and genetic risk factors. Combined effects of MMP-7, MMP-8 and MMP-26 on the risk of IS remain incompletely understood. We aimed to assess individual and joint effects for IS risk by weighted genetic risk score (wGRS) from these three genes and traditional CVD risk factors. A case-control study including 500 cases with IS and 500 stroke-free healthy controls frequency-matched with cases by age and sex was conducted. The wGRS was a weighted average of the number of risk genotype across selected SNPs from MMP-7, MMP-8 and MMP-26. Multivariate logistic regression models were used to analyze the relationship between wGRS and risk of IS. A wGRS in the second tertile was associated with a 1.5-fold increased risk of IS compared with the lowest tertile after adjusting for traditional CVD risk factors. Compared to subjects with low genetic and low modifiable CVD risk, those with high genetic and high modifiable CVD risk had the highest risk of IS (adjusted-OR = 5.75). In conclusion, higher wGRS was significantly associated with an increased risk for IS. A significant interaction between genetic and traditional CVD risk factors was also found on the risk of IS. |
format | Online Article Text |
id | pubmed-6912324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69123242020-01-02 Combined Effects of MMP-7, MMP-8 and MMP-26 on the Risk of Ischemic Stroke Hsieh, Fang-I Chiou, Hung-Yi Hu, Chaur-Jong Jeng, Jiann-Shing Lin, Huey-Juan Lee, Jiunn-Tay Lien, Li-Ming J Clin Med Article Ischemic stroke (IS) is multifactorial causation combining with traditional cardiovascular disease (CVD) and genetic risk factors. Combined effects of MMP-7, MMP-8 and MMP-26 on the risk of IS remain incompletely understood. We aimed to assess individual and joint effects for IS risk by weighted genetic risk score (wGRS) from these three genes and traditional CVD risk factors. A case-control study including 500 cases with IS and 500 stroke-free healthy controls frequency-matched with cases by age and sex was conducted. The wGRS was a weighted average of the number of risk genotype across selected SNPs from MMP-7, MMP-8 and MMP-26. Multivariate logistic regression models were used to analyze the relationship between wGRS and risk of IS. A wGRS in the second tertile was associated with a 1.5-fold increased risk of IS compared with the lowest tertile after adjusting for traditional CVD risk factors. Compared to subjects with low genetic and low modifiable CVD risk, those with high genetic and high modifiable CVD risk had the highest risk of IS (adjusted-OR = 5.75). In conclusion, higher wGRS was significantly associated with an increased risk for IS. A significant interaction between genetic and traditional CVD risk factors was also found on the risk of IS. MDPI 2019-11-18 /pmc/articles/PMC6912324/ /pubmed/31752174 http://dx.doi.org/10.3390/jcm8112011 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hsieh, Fang-I Chiou, Hung-Yi Hu, Chaur-Jong Jeng, Jiann-Shing Lin, Huey-Juan Lee, Jiunn-Tay Lien, Li-Ming Combined Effects of MMP-7, MMP-8 and MMP-26 on the Risk of Ischemic Stroke |
title | Combined Effects of MMP-7, MMP-8 and MMP-26 on the Risk of Ischemic Stroke |
title_full | Combined Effects of MMP-7, MMP-8 and MMP-26 on the Risk of Ischemic Stroke |
title_fullStr | Combined Effects of MMP-7, MMP-8 and MMP-26 on the Risk of Ischemic Stroke |
title_full_unstemmed | Combined Effects of MMP-7, MMP-8 and MMP-26 on the Risk of Ischemic Stroke |
title_short | Combined Effects of MMP-7, MMP-8 and MMP-26 on the Risk of Ischemic Stroke |
title_sort | combined effects of mmp-7, mmp-8 and mmp-26 on the risk of ischemic stroke |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912324/ https://www.ncbi.nlm.nih.gov/pubmed/31752174 http://dx.doi.org/10.3390/jcm8112011 |
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