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Sex‐specific associations of cardiorespiratory fitness and galectin‐3 in the general population
AIMS: Low cardiorespiratory fitness (CRF) is associated with greater mortality and morbidity. Galectin‐3 (Gal‐3) is a prognostic biomarker for fibrosis and heart failure. Gal‐3 is also associated with a greater risk for cardiovascular mortality. Whether CRF is related with Gal‐3 is unclear. The obje...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773777/ https://www.ncbi.nlm.nih.gov/pubmed/36113868 http://dx.doi.org/10.1002/ehf2.14151 |
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author | Haid, Magdalena E. Zylla, Stephanie Paulista Markus, Marcello Ricardo Friedrich, Nele Ewert, Ralf Gläser, Sven Felix, Stephan B. Dörr, Marcus Bahls, Martin |
author_facet | Haid, Magdalena E. Zylla, Stephanie Paulista Markus, Marcello Ricardo Friedrich, Nele Ewert, Ralf Gläser, Sven Felix, Stephan B. Dörr, Marcus Bahls, Martin |
author_sort | Haid, Magdalena E. |
collection | PubMed |
description | AIMS: Low cardiorespiratory fitness (CRF) is associated with greater mortality and morbidity. Galectin‐3 (Gal‐3) is a prognostic biomarker for fibrosis and heart failure. Gal‐3 is also associated with a greater risk for cardiovascular mortality. Whether CRF is related with Gal‐3 is unclear. The objective of this study was to assess the sex‐specific associations of CRF and Gal‐3 levels in the general population. METHODS: Gal‐3 concentrations were determined using a sandwich enzyme immunoassay in the population‐based Study of Health in Pomerania (SHIP‐TREND‐0). Sex‐stratified linear regression models adjusted for age, current smoking status, and renal function were used. Individuals with left ventricular ejection fraction (LVEF) <40%, previous myocardial infarction, atrial fibrillation, chronic lung disease, severe renal disease (estimated glomerular filtration rate <30 mL/min/mm(2)), a history of cancer, and extreme values for Gal‐3 (<1st percentile; >99th percentile) were excluded. RESULTS: A total of n = 1515 participants with a median age of 49 (IQR: 39–60 years, 48% males) were included. In men, a 1 L/min greater VO(2)peak was significantly related to 0.50 ng/mL (95% CI −0.8068 to −0.1938, P < 0.01) less Gal‐3. In males, a 1 mL/min/kg higher VO(2)peak adjusted for body weight was associated with −0.0286 ng/mL (95% CI −0.0052 to −0.0005, P = 0.02) less Gal‐3. When VO(2)peak was adjusted for lean mass 1 mL/kg/min more was correlated with a −0.0022 ng/mL (95% CI −0.0043 to ‐0.0007, P = 0.04) less Gal‐3. In women, VO(2)peak (β −0.2046 95% CI −0.6541 to 0.2449, P = 0.37) and VO(2)peak adjusted for lean mass (β −0.0019 95% CI −0.0421 to –0.0050, P = 0.12) were not related with Gal‐3, whereas a 1 mL/min/kg higher VO(2)peak adjusted for body weight was significantly associated with a −0.0064 ng/mL lower Gal‐3 (95% CI −0.0092 to ‐0.0035, P < 0.01). There were no differences between pre‐menopausal and post‐menopausal women. CONCLUSIONS: VO(2)peak was associated with Gal‐3 only in men, but VO(2)peak adjusted for body weight in women and men. Our results suggest that the adverse consequences of low CRF may be mediated by Gal‐3. Further research is needed to understand the sex‐specific association between CRF and Gal‐3 and whether they are clinically relevant. |
format | Online Article Text |
id | pubmed-9773777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97737772022-12-23 Sex‐specific associations of cardiorespiratory fitness and galectin‐3 in the general population Haid, Magdalena E. Zylla, Stephanie Paulista Markus, Marcello Ricardo Friedrich, Nele Ewert, Ralf Gläser, Sven Felix, Stephan B. Dörr, Marcus Bahls, Martin ESC Heart Fail Original Articles AIMS: Low cardiorespiratory fitness (CRF) is associated with greater mortality and morbidity. Galectin‐3 (Gal‐3) is a prognostic biomarker for fibrosis and heart failure. Gal‐3 is also associated with a greater risk for cardiovascular mortality. Whether CRF is related with Gal‐3 is unclear. The objective of this study was to assess the sex‐specific associations of CRF and Gal‐3 levels in the general population. METHODS: Gal‐3 concentrations were determined using a sandwich enzyme immunoassay in the population‐based Study of Health in Pomerania (SHIP‐TREND‐0). Sex‐stratified linear regression models adjusted for age, current smoking status, and renal function were used. Individuals with left ventricular ejection fraction (LVEF) <40%, previous myocardial infarction, atrial fibrillation, chronic lung disease, severe renal disease (estimated glomerular filtration rate <30 mL/min/mm(2)), a history of cancer, and extreme values for Gal‐3 (<1st percentile; >99th percentile) were excluded. RESULTS: A total of n = 1515 participants with a median age of 49 (IQR: 39–60 years, 48% males) were included. In men, a 1 L/min greater VO(2)peak was significantly related to 0.50 ng/mL (95% CI −0.8068 to −0.1938, P < 0.01) less Gal‐3. In males, a 1 mL/min/kg higher VO(2)peak adjusted for body weight was associated with −0.0286 ng/mL (95% CI −0.0052 to −0.0005, P = 0.02) less Gal‐3. When VO(2)peak was adjusted for lean mass 1 mL/kg/min more was correlated with a −0.0022 ng/mL (95% CI −0.0043 to ‐0.0007, P = 0.04) less Gal‐3. In women, VO(2)peak (β −0.2046 95% CI −0.6541 to 0.2449, P = 0.37) and VO(2)peak adjusted for lean mass (β −0.0019 95% CI −0.0421 to –0.0050, P = 0.12) were not related with Gal‐3, whereas a 1 mL/min/kg higher VO(2)peak adjusted for body weight was significantly associated with a −0.0064 ng/mL lower Gal‐3 (95% CI −0.0092 to ‐0.0035, P < 0.01). There were no differences between pre‐menopausal and post‐menopausal women. CONCLUSIONS: VO(2)peak was associated with Gal‐3 only in men, but VO(2)peak adjusted for body weight in women and men. Our results suggest that the adverse consequences of low CRF may be mediated by Gal‐3. Further research is needed to understand the sex‐specific association between CRF and Gal‐3 and whether they are clinically relevant. John Wiley and Sons Inc. 2022-09-16 /pmc/articles/PMC9773777/ /pubmed/36113868 http://dx.doi.org/10.1002/ehf2.14151 Text en © 2022 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Haid, Magdalena E. Zylla, Stephanie Paulista Markus, Marcello Ricardo Friedrich, Nele Ewert, Ralf Gläser, Sven Felix, Stephan B. Dörr, Marcus Bahls, Martin Sex‐specific associations of cardiorespiratory fitness and galectin‐3 in the general population |
title | Sex‐specific associations of cardiorespiratory fitness and galectin‐3 in the general population |
title_full | Sex‐specific associations of cardiorespiratory fitness and galectin‐3 in the general population |
title_fullStr | Sex‐specific associations of cardiorespiratory fitness and galectin‐3 in the general population |
title_full_unstemmed | Sex‐specific associations of cardiorespiratory fitness and galectin‐3 in the general population |
title_short | Sex‐specific associations of cardiorespiratory fitness and galectin‐3 in the general population |
title_sort | sex‐specific associations of cardiorespiratory fitness and galectin‐3 in the general population |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773777/ https://www.ncbi.nlm.nih.gov/pubmed/36113868 http://dx.doi.org/10.1002/ehf2.14151 |
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