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Circulating levels of adiponectin and extent of coronary artery disease in patients undergoing elective coronary angiography
Adiponectin (APN), an adipose tissue-released adipokine with demonstrated anti-inflammatory and anti-atherogenic properties, is encoded by a gene whose polymorphisms are associated with presence of coronary artery disease (CAD). Serum APN levels are inversely related with presence and complexity of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Divulgação Científica
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711007/ https://www.ncbi.nlm.nih.gov/pubmed/29211251 http://dx.doi.org/10.1590/1414-431X20176738 |
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author | Souza, R.A. Alves, C.M.R. de Oliveira, C.S.V. Reis, A.F. Carvalho, A.C. |
author_facet | Souza, R.A. Alves, C.M.R. de Oliveira, C.S.V. Reis, A.F. Carvalho, A.C. |
author_sort | Souza, R.A. |
collection | PubMed |
description | Adiponectin (APN), an adipose tissue-released adipokine with demonstrated anti-inflammatory and anti-atherogenic properties, is encoded by a gene whose polymorphisms are associated with presence of coronary artery disease (CAD). Serum APN levels are inversely related with presence and complexity of CAD. Within this context, we sought to compare levels of total APN and its high molecular weight form (HMW APN) according to clinical presentation and extent of CAD in patients undergoing elective cardiac catheterization. From March 2008 to June 2010, clinical data and blood samples for APN and HMW APN measurements were collected from 415 subjects undergoing cardiac catheterization at two tertiary centers. CAD extent was estimated by the number of coronary arteries with significant stenosis (≥70% obstruction in a major coronary artery) and by Duke Jeopardy Score (DJS). Serum APN levels were similar between groups with stable or unstable CAD (APN 9.20±5.88 vs 9.47±6.23 μg/mL, P=0.738, and HMW APN 5.31±3.72 vs 5.91±4.16 μg/mL, P=0.255), even after stratification by the number of arteries involved (single-vessel vs multivessel disease: APN 9.39±5.76 vs 9.26±6.27 μg/mL, P=0.871; HMW APN 5.29±3.79 vs 5.83±4.04 μg/mL, P=0.306) and DJS score (APN, P=0.718; HMW APN, P=0.276). We conclude that APN and HMW APN serum levels are similar across clinical presentations and different extents of CAD, despite being significantly lower in the presence of obstructive CAD. |
format | Online Article Text |
id | pubmed-5711007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Associação Brasileira de Divulgação Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-57110072017-12-08 Circulating levels of adiponectin and extent of coronary artery disease in patients undergoing elective coronary angiography Souza, R.A. Alves, C.M.R. de Oliveira, C.S.V. Reis, A.F. Carvalho, A.C. Braz J Med Biol Res Research Articles Adiponectin (APN), an adipose tissue-released adipokine with demonstrated anti-inflammatory and anti-atherogenic properties, is encoded by a gene whose polymorphisms are associated with presence of coronary artery disease (CAD). Serum APN levels are inversely related with presence and complexity of CAD. Within this context, we sought to compare levels of total APN and its high molecular weight form (HMW APN) according to clinical presentation and extent of CAD in patients undergoing elective cardiac catheterization. From March 2008 to June 2010, clinical data and blood samples for APN and HMW APN measurements were collected from 415 subjects undergoing cardiac catheterization at two tertiary centers. CAD extent was estimated by the number of coronary arteries with significant stenosis (≥70% obstruction in a major coronary artery) and by Duke Jeopardy Score (DJS). Serum APN levels were similar between groups with stable or unstable CAD (APN 9.20±5.88 vs 9.47±6.23 μg/mL, P=0.738, and HMW APN 5.31±3.72 vs 5.91±4.16 μg/mL, P=0.255), even after stratification by the number of arteries involved (single-vessel vs multivessel disease: APN 9.39±5.76 vs 9.26±6.27 μg/mL, P=0.871; HMW APN 5.29±3.79 vs 5.83±4.04 μg/mL, P=0.306) and DJS score (APN, P=0.718; HMW APN, P=0.276). We conclude that APN and HMW APN serum levels are similar across clinical presentations and different extents of CAD, despite being significantly lower in the presence of obstructive CAD. Associação Brasileira de Divulgação Científica 2017-11-30 /pmc/articles/PMC5711007/ /pubmed/29211251 http://dx.doi.org/10.1590/1414-431X20176738 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Souza, R.A. Alves, C.M.R. de Oliveira, C.S.V. Reis, A.F. Carvalho, A.C. Circulating levels of adiponectin and extent of coronary artery disease in patients undergoing elective coronary angiography |
title | Circulating levels of adiponectin and extent of coronary artery disease in patients undergoing elective coronary angiography |
title_full | Circulating levels of adiponectin and extent of coronary artery disease in patients undergoing elective coronary angiography |
title_fullStr | Circulating levels of adiponectin and extent of coronary artery disease in patients undergoing elective coronary angiography |
title_full_unstemmed | Circulating levels of adiponectin and extent of coronary artery disease in patients undergoing elective coronary angiography |
title_short | Circulating levels of adiponectin and extent of coronary artery disease in patients undergoing elective coronary angiography |
title_sort | circulating levels of adiponectin and extent of coronary artery disease in patients undergoing elective coronary angiography |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711007/ https://www.ncbi.nlm.nih.gov/pubmed/29211251 http://dx.doi.org/10.1590/1414-431X20176738 |
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