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Association between elevated adiponectin level and adverse outcomes in patients with heart failure: a systematic review and meta-analysis
Studies regarding the prognostic value of circulating adiponectin level in patients with heart failure are conflicting. The aim of this meta-analysis was to evaluate the association between elevated circulating adiponectin level and adverse outcomes in patients with heart failure. We searched PubMed...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Divulgação Científica
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644532/ https://www.ncbi.nlm.nih.gov/pubmed/31314851 http://dx.doi.org/10.1590/1414-431X20198416 |
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author | Bai, Wenwei Huang, Jingjing Zhu, Min Liu, Xiaoyong Tao, Jianping |
author_facet | Bai, Wenwei Huang, Jingjing Zhu, Min Liu, Xiaoyong Tao, Jianping |
author_sort | Bai, Wenwei |
collection | PubMed |
description | Studies regarding the prognostic value of circulating adiponectin level in patients with heart failure are conflicting. The aim of this meta-analysis was to evaluate the association between elevated circulating adiponectin level and adverse outcomes in patients with heart failure. We searched PubMed and Embase databases from their inception to June 2018. Original observational studies that investigated the prognostic value of adiponectin in heart failure patients and reported all-cause mortality or combined endpoints of death/readmission as outcome measure were included. Pooled risk ratio (RR) with 95% confidence intervals (CI) were estimated by higher versus lower circulating adiponectin level. A total of 7 studies involving 862 heart failure patients were identified. Meta-analysis showed that heart failure patients with higher adiponectin level had significantly increased risk of all-cause mortality (RR 2.05; 95%CI 1.22–3.43) after adjustment for potential confounders. In addition, higher adiponectin level was associated with an increased risk of the combined endpoints of death/readmission (RR 2.22; 95%CI 1.38–3.57). Elevated baseline circulating adiponectin level is possibly associated with an increased risk of all-cause mortality and the combined endpoints of death/readmission in patients with heart failure. Determination of circulating adiponectin level has potential to improve risk stratification in heart failure patients. |
format | Online Article Text |
id | pubmed-6644532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Associação Brasileira de Divulgação Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-66445322019-08-07 Association between elevated adiponectin level and adverse outcomes in patients with heart failure: a systematic review and meta-analysis Bai, Wenwei Huang, Jingjing Zhu, Min Liu, Xiaoyong Tao, Jianping Braz J Med Biol Res Research Article Studies regarding the prognostic value of circulating adiponectin level in patients with heart failure are conflicting. The aim of this meta-analysis was to evaluate the association between elevated circulating adiponectin level and adverse outcomes in patients with heart failure. We searched PubMed and Embase databases from their inception to June 2018. Original observational studies that investigated the prognostic value of adiponectin in heart failure patients and reported all-cause mortality or combined endpoints of death/readmission as outcome measure were included. Pooled risk ratio (RR) with 95% confidence intervals (CI) were estimated by higher versus lower circulating adiponectin level. A total of 7 studies involving 862 heart failure patients were identified. Meta-analysis showed that heart failure patients with higher adiponectin level had significantly increased risk of all-cause mortality (RR 2.05; 95%CI 1.22–3.43) after adjustment for potential confounders. In addition, higher adiponectin level was associated with an increased risk of the combined endpoints of death/readmission (RR 2.22; 95%CI 1.38–3.57). Elevated baseline circulating adiponectin level is possibly associated with an increased risk of all-cause mortality and the combined endpoints of death/readmission in patients with heart failure. Determination of circulating adiponectin level has potential to improve risk stratification in heart failure patients. Associação Brasileira de Divulgação Científica 2019-07-15 /pmc/articles/PMC6644532/ /pubmed/31314851 http://dx.doi.org/10.1590/1414-431X20198416 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bai, Wenwei Huang, Jingjing Zhu, Min Liu, Xiaoyong Tao, Jianping Association between elevated adiponectin level and adverse outcomes in patients with heart failure: a systematic review and meta-analysis |
title | Association between elevated adiponectin level and adverse outcomes
in patients with heart failure: a systematic review and
meta-analysis |
title_full | Association between elevated adiponectin level and adverse outcomes
in patients with heart failure: a systematic review and
meta-analysis |
title_fullStr | Association between elevated adiponectin level and adverse outcomes
in patients with heart failure: a systematic review and
meta-analysis |
title_full_unstemmed | Association between elevated adiponectin level and adverse outcomes
in patients with heart failure: a systematic review and
meta-analysis |
title_short | Association between elevated adiponectin level and adverse outcomes
in patients with heart failure: a systematic review and
meta-analysis |
title_sort | association between elevated adiponectin level and adverse outcomes
in patients with heart failure: a systematic review and
meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644532/ https://www.ncbi.nlm.nih.gov/pubmed/31314851 http://dx.doi.org/10.1590/1414-431X20198416 |
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