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Plasma GDF-15 concentration is not elevated in open-angle glaucoma

AIM: Recently, the level of growth differentiation factor 15 (GDF-15) in blood, was proposed as biomarker to detect mitochondrial dysfunction. In the current study, we evaluate this biomarker in open-angle glaucoma (OAG), as there is increasing evidence that mitochondrial dysfunction plays a role in...

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Autores principales: Hubens, Wouter H. G., Kievit, Mariëlle T., Berendschot, Tos T. J. M., de Coo, Irenaeus F. M., Smeets, Hubert J. M., Webers, Carroll A. B., Gorgels, Theo G. M. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162581/
https://www.ncbi.nlm.nih.gov/pubmed/34048486
http://dx.doi.org/10.1371/journal.pone.0252630
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author Hubens, Wouter H. G.
Kievit, Mariëlle T.
Berendschot, Tos T. J. M.
de Coo, Irenaeus F. M.
Smeets, Hubert J. M.
Webers, Carroll A. B.
Gorgels, Theo G. M. F.
author_facet Hubens, Wouter H. G.
Kievit, Mariëlle T.
Berendschot, Tos T. J. M.
de Coo, Irenaeus F. M.
Smeets, Hubert J. M.
Webers, Carroll A. B.
Gorgels, Theo G. M. F.
author_sort Hubens, Wouter H. G.
collection PubMed
description AIM: Recently, the level of growth differentiation factor 15 (GDF-15) in blood, was proposed as biomarker to detect mitochondrial dysfunction. In the current study, we evaluate this biomarker in open-angle glaucoma (OAG), as there is increasing evidence that mitochondrial dysfunction plays a role in the pathophysiology of this disease. METHODS: Plasma GDF-15 concentrations were measured with ELISA in 200 OAG patients and 61 age-matched controls (cataract without glaucoma). The OAG patient group consisted of high tension glaucoma (HTG; n = 162) and normal tension glaucoma (NTG; n = 38). Groups were compared using the Kruskal-Wallis nonparametric test with Dunn’s multiple comparison post-hoc correction. GDF-15 concentration was corrected for confounders identified with forward linear regression models. RESULTS: Before correcting for confounders, median plasma GDF-15 levels was significantly lower in the combined OAG group (p = 0.04), but not when analysing HTG and NTG patients separately. Forward linear regression analysis showed that age, gender, smoking and systemic hypertension were significant confounders affecting GDF-15 levels. After correction for these confounders, GDF-15 levels in OAG patients were no longer significantly different from controls. Subgroup analysis of the glaucoma patients did not show a correlation between disease severity and plasma GDF-15, but did reveal that for NTG patients, intake of dietary supplements, which potentially improve mitochondrial function, correlated with lower plasma GDF-15. CONCLUSION: The present study suggests that plasma GDF-15 is not suited as biomarker of mitochondrial dysfunction in OAG patients.
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spelling pubmed-81625812021-06-10 Plasma GDF-15 concentration is not elevated in open-angle glaucoma Hubens, Wouter H. G. Kievit, Mariëlle T. Berendschot, Tos T. J. M. de Coo, Irenaeus F. M. Smeets, Hubert J. M. Webers, Carroll A. B. Gorgels, Theo G. M. F. PLoS One Research Article AIM: Recently, the level of growth differentiation factor 15 (GDF-15) in blood, was proposed as biomarker to detect mitochondrial dysfunction. In the current study, we evaluate this biomarker in open-angle glaucoma (OAG), as there is increasing evidence that mitochondrial dysfunction plays a role in the pathophysiology of this disease. METHODS: Plasma GDF-15 concentrations were measured with ELISA in 200 OAG patients and 61 age-matched controls (cataract without glaucoma). The OAG patient group consisted of high tension glaucoma (HTG; n = 162) and normal tension glaucoma (NTG; n = 38). Groups were compared using the Kruskal-Wallis nonparametric test with Dunn’s multiple comparison post-hoc correction. GDF-15 concentration was corrected for confounders identified with forward linear regression models. RESULTS: Before correcting for confounders, median plasma GDF-15 levels was significantly lower in the combined OAG group (p = 0.04), but not when analysing HTG and NTG patients separately. Forward linear regression analysis showed that age, gender, smoking and systemic hypertension were significant confounders affecting GDF-15 levels. After correction for these confounders, GDF-15 levels in OAG patients were no longer significantly different from controls. Subgroup analysis of the glaucoma patients did not show a correlation between disease severity and plasma GDF-15, but did reveal that for NTG patients, intake of dietary supplements, which potentially improve mitochondrial function, correlated with lower plasma GDF-15. CONCLUSION: The present study suggests that plasma GDF-15 is not suited as biomarker of mitochondrial dysfunction in OAG patients. Public Library of Science 2021-05-28 /pmc/articles/PMC8162581/ /pubmed/34048486 http://dx.doi.org/10.1371/journal.pone.0252630 Text en © 2021 Hubens et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hubens, Wouter H. G.
Kievit, Mariëlle T.
Berendschot, Tos T. J. M.
de Coo, Irenaeus F. M.
Smeets, Hubert J. M.
Webers, Carroll A. B.
Gorgels, Theo G. M. F.
Plasma GDF-15 concentration is not elevated in open-angle glaucoma
title Plasma GDF-15 concentration is not elevated in open-angle glaucoma
title_full Plasma GDF-15 concentration is not elevated in open-angle glaucoma
title_fullStr Plasma GDF-15 concentration is not elevated in open-angle glaucoma
title_full_unstemmed Plasma GDF-15 concentration is not elevated in open-angle glaucoma
title_short Plasma GDF-15 concentration is not elevated in open-angle glaucoma
title_sort plasma gdf-15 concentration is not elevated in open-angle glaucoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162581/
https://www.ncbi.nlm.nih.gov/pubmed/34048486
http://dx.doi.org/10.1371/journal.pone.0252630
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