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Association of growth differentiation factor-15 level with adverse outcomes in patients with stable coronary artery disease: A meta-analysis
BACKGROUND AND AIMS: Studies on the association between growth-differentiation factor-15 (GDF-15) level and adverse outcomes have yielded conflicting results in patients with stable coronary artery disease (CAD). This meta-analysis aimed to evaluate the association of baseline GDF-15 level with adve...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9833259/ https://www.ncbi.nlm.nih.gov/pubmed/36643602 http://dx.doi.org/10.1016/j.athplu.2021.11.003 |
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author | Li, Tingjian Chen, Youjin Ye, Tingting Zheng, Lin Chen, Luo Fan, Yuncao Lin, Bin |
author_facet | Li, Tingjian Chen, Youjin Ye, Tingting Zheng, Lin Chen, Luo Fan, Yuncao Lin, Bin |
author_sort | Li, Tingjian |
collection | PubMed |
description | BACKGROUND AND AIMS: Studies on the association between growth-differentiation factor-15 (GDF-15) level and adverse outcomes have yielded conflicting results in patients with stable coronary artery disease (CAD). This meta-analysis aimed to evaluate the association of baseline GDF-15 level with adverse outcomes in stable CAD patients. METHODS: Two authors independently searched PubMed and Embase databases from inception to May 31, 2021 for available studies that investigated the association of baseline GDF-15 level with all-cause mortality, cardiovascular mortality, or major adverse cardiovascular events (MACEs) in stable CAD patients. Pooled multivariable adjusted hazard ratio (HR) with 95% confidence interval (CI) was calculated for the highest vs. the lowest GDF-15 level. RESULTS: Seven studies that involved 28,765 stable CAD patients were identified and analyzed. The meta-analysis showed that the highest GDF-15 level was associated with higher risk of MACEs (HR 1.42; 95% CI 1.29–1.57; p < 0.001), cardiovascular mortality (HR 1.64: 95% CI 1.25–2.14; p < 0.001), and all-cause mortality (HR 2.01; 95% CI 1.67–2.42; p < 0.001) when compared the lowest GDF-15 level. Moreover, the values of GDF-15 level in predicting MACEs were consistently observed in each named subgroup. CONCLUSIONS: Elevated blood GDF-15 level is an independent predictor of MACEs, cardiovascular mortality, and all-cause mortality in stable CAD patients. The baseline GDF-15 level may play an important role in the risk stratification of stable CAD patients. |
format | Online Article Text |
id | pubmed-9833259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98332592023-01-12 Association of growth differentiation factor-15 level with adverse outcomes in patients with stable coronary artery disease: A meta-analysis Li, Tingjian Chen, Youjin Ye, Tingting Zheng, Lin Chen, Luo Fan, Yuncao Lin, Bin Atheroscler Plus Article BACKGROUND AND AIMS: Studies on the association between growth-differentiation factor-15 (GDF-15) level and adverse outcomes have yielded conflicting results in patients with stable coronary artery disease (CAD). This meta-analysis aimed to evaluate the association of baseline GDF-15 level with adverse outcomes in stable CAD patients. METHODS: Two authors independently searched PubMed and Embase databases from inception to May 31, 2021 for available studies that investigated the association of baseline GDF-15 level with all-cause mortality, cardiovascular mortality, or major adverse cardiovascular events (MACEs) in stable CAD patients. Pooled multivariable adjusted hazard ratio (HR) with 95% confidence interval (CI) was calculated for the highest vs. the lowest GDF-15 level. RESULTS: Seven studies that involved 28,765 stable CAD patients were identified and analyzed. The meta-analysis showed that the highest GDF-15 level was associated with higher risk of MACEs (HR 1.42; 95% CI 1.29–1.57; p < 0.001), cardiovascular mortality (HR 1.64: 95% CI 1.25–2.14; p < 0.001), and all-cause mortality (HR 2.01; 95% CI 1.67–2.42; p < 0.001) when compared the lowest GDF-15 level. Moreover, the values of GDF-15 level in predicting MACEs were consistently observed in each named subgroup. CONCLUSIONS: Elevated blood GDF-15 level is an independent predictor of MACEs, cardiovascular mortality, and all-cause mortality in stable CAD patients. The baseline GDF-15 level may play an important role in the risk stratification of stable CAD patients. Elsevier 2021-12-06 /pmc/articles/PMC9833259/ /pubmed/36643602 http://dx.doi.org/10.1016/j.athplu.2021.11.003 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Li, Tingjian Chen, Youjin Ye, Tingting Zheng, Lin Chen, Luo Fan, Yuncao Lin, Bin Association of growth differentiation factor-15 level with adverse outcomes in patients with stable coronary artery disease: A meta-analysis |
title | Association of growth differentiation factor-15 level with adverse outcomes in patients with stable coronary artery disease: A meta-analysis |
title_full | Association of growth differentiation factor-15 level with adverse outcomes in patients with stable coronary artery disease: A meta-analysis |
title_fullStr | Association of growth differentiation factor-15 level with adverse outcomes in patients with stable coronary artery disease: A meta-analysis |
title_full_unstemmed | Association of growth differentiation factor-15 level with adverse outcomes in patients with stable coronary artery disease: A meta-analysis |
title_short | Association of growth differentiation factor-15 level with adverse outcomes in patients with stable coronary artery disease: A meta-analysis |
title_sort | association of growth differentiation factor-15 level with adverse outcomes in patients with stable coronary artery disease: a meta-analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9833259/ https://www.ncbi.nlm.nih.gov/pubmed/36643602 http://dx.doi.org/10.1016/j.athplu.2021.11.003 |
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