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Association between ADAMTS7 polymorphism and carotid artery plaque vulnerability
Recent genome-wide association studies (GWAS) indicated that polymorphisms in ADAMTS7 were associated with artery disease caused by atherosclerosis. However, the correlation between the ADAMTS7 polymorphism and plaque stability remains unclear. The objective of this study was to evaluate the associa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824807/ https://www.ncbi.nlm.nih.gov/pubmed/31651847 http://dx.doi.org/10.1097/MD.0000000000017438 |
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author | Li, Hao-wen Shen, Mi Gao, Pei-yi Li, Zi-rui Cao, Jing-li Zhang, Wen-li Sui, Bin-bin Wang, Yu-xin Wang, Ya-jie |
author_facet | Li, Hao-wen Shen, Mi Gao, Pei-yi Li, Zi-rui Cao, Jing-li Zhang, Wen-li Sui, Bin-bin Wang, Yu-xin Wang, Ya-jie |
author_sort | Li, Hao-wen |
collection | PubMed |
description | Recent genome-wide association studies (GWAS) indicated that polymorphisms in ADAMTS7 were associated with artery disease caused by atherosclerosis. However, the correlation between the ADAMTS7 polymorphism and plaque stability remains unclear. The objective of this study was to evaluate the association between 2 ADAMTS7 variants rs3825807 and rs7173743 and ischemic stroke or atherosclerotic plaque vulnerability. This research is an observational study. Patients with ischemic stroke and normal control individuals admitted to Beijing Tiantan Hospital from May 2014 to October 2017 were enrolled. High-resolution magnetic resonance imaging was used to distinguish vulnerable and stable carotid plaques. The ADAMTS7 SNPs were genotyped using TaqMan assays on real-time PCR system. The multivariate logistic regression analyses were used to adjust for multiple risk factors between groups. Three hundred twenty-six patients with ischemic stroke (189 patients with vulnerable plaque and 81 patients with stable plaque) and 432 normal controls were included. ADAMTS7 polymorphisms of both rs7173743 and rs3825807 were associated with carotid plaque vulnerability but not the prevalence of ischemic stroke. The T/T genotype of rs7173743 [odds ratio (OR) = 1.885, 95% confidence interval (CI) = 1.067–3.328, P = .028] and A/A genotype of rs3825807 (OR = 2.146, 95% CI = 1.163–3.961, P = .013) were considered as risk genotypes for vulnerable plaque susceptibility. In conclusion, ADAMTS7 variants rs3825807 and rs7173743 are associated with the risk for carotid plaque vulnerability. |
format | Online Article Text |
id | pubmed-6824807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-68248072019-11-19 Association between ADAMTS7 polymorphism and carotid artery plaque vulnerability Li, Hao-wen Shen, Mi Gao, Pei-yi Li, Zi-rui Cao, Jing-li Zhang, Wen-li Sui, Bin-bin Wang, Yu-xin Wang, Ya-jie Medicine (Baltimore) 3500 Recent genome-wide association studies (GWAS) indicated that polymorphisms in ADAMTS7 were associated with artery disease caused by atherosclerosis. However, the correlation between the ADAMTS7 polymorphism and plaque stability remains unclear. The objective of this study was to evaluate the association between 2 ADAMTS7 variants rs3825807 and rs7173743 and ischemic stroke or atherosclerotic plaque vulnerability. This research is an observational study. Patients with ischemic stroke and normal control individuals admitted to Beijing Tiantan Hospital from May 2014 to October 2017 were enrolled. High-resolution magnetic resonance imaging was used to distinguish vulnerable and stable carotid plaques. The ADAMTS7 SNPs were genotyped using TaqMan assays on real-time PCR system. The multivariate logistic regression analyses were used to adjust for multiple risk factors between groups. Three hundred twenty-six patients with ischemic stroke (189 patients with vulnerable plaque and 81 patients with stable plaque) and 432 normal controls were included. ADAMTS7 polymorphisms of both rs7173743 and rs3825807 were associated with carotid plaque vulnerability but not the prevalence of ischemic stroke. The T/T genotype of rs7173743 [odds ratio (OR) = 1.885, 95% confidence interval (CI) = 1.067–3.328, P = .028] and A/A genotype of rs3825807 (OR = 2.146, 95% CI = 1.163–3.961, P = .013) were considered as risk genotypes for vulnerable plaque susceptibility. In conclusion, ADAMTS7 variants rs3825807 and rs7173743 are associated with the risk for carotid plaque vulnerability. Wolters Kluwer Health 2019-10-25 /pmc/articles/PMC6824807/ /pubmed/31651847 http://dx.doi.org/10.1097/MD.0000000000017438 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 3500 Li, Hao-wen Shen, Mi Gao, Pei-yi Li, Zi-rui Cao, Jing-li Zhang, Wen-li Sui, Bin-bin Wang, Yu-xin Wang, Ya-jie Association between ADAMTS7 polymorphism and carotid artery plaque vulnerability |
title | Association between ADAMTS7 polymorphism and carotid artery plaque vulnerability |
title_full | Association between ADAMTS7 polymorphism and carotid artery plaque vulnerability |
title_fullStr | Association between ADAMTS7 polymorphism and carotid artery plaque vulnerability |
title_full_unstemmed | Association between ADAMTS7 polymorphism and carotid artery plaque vulnerability |
title_short | Association between ADAMTS7 polymorphism and carotid artery plaque vulnerability |
title_sort | association between adamts7 polymorphism and carotid artery plaque vulnerability |
topic | 3500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824807/ https://www.ncbi.nlm.nih.gov/pubmed/31651847 http://dx.doi.org/10.1097/MD.0000000000017438 |
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