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Proprotein convertase subtilisin/kexin type 9 levels and aortic valve calcification: A prospective, cross sectional study
OBJECTIVE: To investigate the possible association between plasma proprotein convertase subtilisin/kexin type 9 (PCSK9) and the incidence and severity of calcific aortic valve disease (CAVD). METHODS: This prospective, cross sectional study involved patients with and without (controls) aortic valve...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536630/ https://www.ncbi.nlm.nih.gov/pubmed/27278556 http://dx.doi.org/10.1177/0300060516648030 |
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author | Wang, Wen-guang He, Yong-feng Chen, Yuan-li Zhao, Fu-mei Song, Yan-qiu Zhang, Hong Ma, Yan-he Guan, Xin Zhang, Wen-ya Chen, Xiao-lin Liu, Chao Cong, Hong-liang |
author_facet | Wang, Wen-guang He, Yong-feng Chen, Yuan-li Zhao, Fu-mei Song, Yan-qiu Zhang, Hong Ma, Yan-he Guan, Xin Zhang, Wen-ya Chen, Xiao-lin Liu, Chao Cong, Hong-liang |
author_sort | Wang, Wen-guang |
collection | PubMed |
description | OBJECTIVE: To investigate the possible association between plasma proprotein convertase subtilisin/kexin type 9 (PCSK9) and the incidence and severity of calcific aortic valve disease (CAVD). METHODS: This prospective, cross sectional study involved patients with and without (controls) aortic valve calcification diagnosed by transthoracic echocardiography and dual source computed tomography (DSCT) scan. Aortic valves calcification scores were calculated from DSCT scans and patients were graded: grade 1, no calcification; grade 2, mildly calcified; grade 3, moderately calcified; grade 4, heavily calcified. Plasma PCSK9 levels were measured using an enzyme-linked immunosorbent assay. RESULTS: Forty patients were grade 1 (controls), 32 were grade 2, 48 were grade 3 and 32 were grade 4. Plasma levels of PCSK9 were significantly different between the four groups and the highest value was observed in the patients with grade 2 calcification. Only low-density lipoprotein cholesterol and lipoprotein (Lp)(a) were associated with the severity of CAVD. Regression analysis showed that age, Lp(a) and PCSK9 were independent predictors of CAVD. CONCLUSION: Data from this cross sectional study in a small sample of patients showed that plasma PCSK9 was correlated with the presence of CAVD but not its severity. |
format | Online Article Text |
id | pubmed-5536630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-55366302017-10-03 Proprotein convertase subtilisin/kexin type 9 levels and aortic valve calcification: A prospective, cross sectional study Wang, Wen-guang He, Yong-feng Chen, Yuan-li Zhao, Fu-mei Song, Yan-qiu Zhang, Hong Ma, Yan-he Guan, Xin Zhang, Wen-ya Chen, Xiao-lin Liu, Chao Cong, Hong-liang J Int Med Res Research Reports OBJECTIVE: To investigate the possible association between plasma proprotein convertase subtilisin/kexin type 9 (PCSK9) and the incidence and severity of calcific aortic valve disease (CAVD). METHODS: This prospective, cross sectional study involved patients with and without (controls) aortic valve calcification diagnosed by transthoracic echocardiography and dual source computed tomography (DSCT) scan. Aortic valves calcification scores were calculated from DSCT scans and patients were graded: grade 1, no calcification; grade 2, mildly calcified; grade 3, moderately calcified; grade 4, heavily calcified. Plasma PCSK9 levels were measured using an enzyme-linked immunosorbent assay. RESULTS: Forty patients were grade 1 (controls), 32 were grade 2, 48 were grade 3 and 32 were grade 4. Plasma levels of PCSK9 were significantly different between the four groups and the highest value was observed in the patients with grade 2 calcification. Only low-density lipoprotein cholesterol and lipoprotein (Lp)(a) were associated with the severity of CAVD. Regression analysis showed that age, Lp(a) and PCSK9 were independent predictors of CAVD. CONCLUSION: Data from this cross sectional study in a small sample of patients showed that plasma PCSK9 was correlated with the presence of CAVD but not its severity. SAGE Publications 2016-06-08 2016-08 /pmc/articles/PMC5536630/ /pubmed/27278556 http://dx.doi.org/10.1177/0300060516648030 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) 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 page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Reports Wang, Wen-guang He, Yong-feng Chen, Yuan-li Zhao, Fu-mei Song, Yan-qiu Zhang, Hong Ma, Yan-he Guan, Xin Zhang, Wen-ya Chen, Xiao-lin Liu, Chao Cong, Hong-liang Proprotein convertase subtilisin/kexin type 9 levels and aortic valve calcification: A prospective, cross sectional study |
title | Proprotein convertase subtilisin/kexin type 9 levels and aortic valve calcification: A prospective, cross sectional study |
title_full | Proprotein convertase subtilisin/kexin type 9 levels and aortic valve calcification: A prospective, cross sectional study |
title_fullStr | Proprotein convertase subtilisin/kexin type 9 levels and aortic valve calcification: A prospective, cross sectional study |
title_full_unstemmed | Proprotein convertase subtilisin/kexin type 9 levels and aortic valve calcification: A prospective, cross sectional study |
title_short | Proprotein convertase subtilisin/kexin type 9 levels and aortic valve calcification: A prospective, cross sectional study |
title_sort | proprotein convertase subtilisin/kexin type 9 levels and aortic valve calcification: a prospective, cross sectional study |
topic | Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536630/ https://www.ncbi.nlm.nih.gov/pubmed/27278556 http://dx.doi.org/10.1177/0300060516648030 |
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