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Plasma C-C Chemokine Concentrations in Intermediate Age-Related Macular Degeneration

Purpose: To determine the relationship between plasma concentrations of the C-C chemokines CCL2, CCL3, CCL4, and CCL5 and intermediate age-related macular degeneration (iAMD) patients compared with control inidividuals to further define the inflammatory pathways associated with age-related macular d...

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Autores principales: Palestine, Alan G., Wagner, Brandie D., Patnaik, Jennifer L., Baldermann, Rebecca, Mathias, Marc T., Mandava, Naresh, Lynch, Anne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636771/
https://www.ncbi.nlm.nih.gov/pubmed/34869411
http://dx.doi.org/10.3389/fmed.2021.710595
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author Palestine, Alan G.
Wagner, Brandie D.
Patnaik, Jennifer L.
Baldermann, Rebecca
Mathias, Marc T.
Mandava, Naresh
Lynch, Anne M.
author_facet Palestine, Alan G.
Wagner, Brandie D.
Patnaik, Jennifer L.
Baldermann, Rebecca
Mathias, Marc T.
Mandava, Naresh
Lynch, Anne M.
author_sort Palestine, Alan G.
collection PubMed
description Purpose: To determine the relationship between plasma concentrations of the C-C chemokines CCL2, CCL3, CCL4, and CCL5 and intermediate age-related macular degeneration (iAMD) patients compared with control inidividuals to further define the inflammatory pathways associated with age-related macular degeneration. Methods: The concentrations of CCL2, CCL3, CCL4, and CCL5 were measured using multiplex assays in plasma collected from 210 patients with iAMD and 102 control individuals with no macular degeneration as defined by multi-modal imaging. Non-inflammatory data included in the analysis were: age, sex, family history of AMD, history of smoking, body mass index, presence of reticular pseudo-drusen and cardiovascular disease. Median concentrations as well as a cutoff value for each chemokine were compared between the two groups. Results: The median concentrations of CCL2 and CCL4 did not differ between control and iAMD groups, however, CCL2 was elevated in iAMD when a cutoff comparison was used (p < 0.05). Median CCL3 and CCL5 concentrations were significantly decreased in the macular degeneration group compared with controls (p < 0.001) as well as when a cutoff value comparison was used. CCL3 and CCL5 were negatively correlated in cases and positively correlated in controls. Conclusions: Plasma CCL3 and CCL5 concentrations were significantly decreased and CCL2 concentrations were increased in patients with iAMD compared with controls, suggesting a role for C-C chemokines in the systemic inflammatory processes associated with disease development.
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spelling pubmed-86367712021-12-03 Plasma C-C Chemokine Concentrations in Intermediate Age-Related Macular Degeneration Palestine, Alan G. Wagner, Brandie D. Patnaik, Jennifer L. Baldermann, Rebecca Mathias, Marc T. Mandava, Naresh Lynch, Anne M. Front Med (Lausanne) Medicine Purpose: To determine the relationship between plasma concentrations of the C-C chemokines CCL2, CCL3, CCL4, and CCL5 and intermediate age-related macular degeneration (iAMD) patients compared with control inidividuals to further define the inflammatory pathways associated with age-related macular degeneration. Methods: The concentrations of CCL2, CCL3, CCL4, and CCL5 were measured using multiplex assays in plasma collected from 210 patients with iAMD and 102 control individuals with no macular degeneration as defined by multi-modal imaging. Non-inflammatory data included in the analysis were: age, sex, family history of AMD, history of smoking, body mass index, presence of reticular pseudo-drusen and cardiovascular disease. Median concentrations as well as a cutoff value for each chemokine were compared between the two groups. Results: The median concentrations of CCL2 and CCL4 did not differ between control and iAMD groups, however, CCL2 was elevated in iAMD when a cutoff comparison was used (p < 0.05). Median CCL3 and CCL5 concentrations were significantly decreased in the macular degeneration group compared with controls (p < 0.001) as well as when a cutoff value comparison was used. CCL3 and CCL5 were negatively correlated in cases and positively correlated in controls. Conclusions: Plasma CCL3 and CCL5 concentrations were significantly decreased and CCL2 concentrations were increased in patients with iAMD compared with controls, suggesting a role for C-C chemokines in the systemic inflammatory processes associated with disease development. Frontiers Media S.A. 2021-11-18 /pmc/articles/PMC8636771/ /pubmed/34869411 http://dx.doi.org/10.3389/fmed.2021.710595 Text en Copyright © 2021 Palestine, Wagner, Patnaik, Baldermann, Mathias, Mandava and Lynch. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Palestine, Alan G.
Wagner, Brandie D.
Patnaik, Jennifer L.
Baldermann, Rebecca
Mathias, Marc T.
Mandava, Naresh
Lynch, Anne M.
Plasma C-C Chemokine Concentrations in Intermediate Age-Related Macular Degeneration
title Plasma C-C Chemokine Concentrations in Intermediate Age-Related Macular Degeneration
title_full Plasma C-C Chemokine Concentrations in Intermediate Age-Related Macular Degeneration
title_fullStr Plasma C-C Chemokine Concentrations in Intermediate Age-Related Macular Degeneration
title_full_unstemmed Plasma C-C Chemokine Concentrations in Intermediate Age-Related Macular Degeneration
title_short Plasma C-C Chemokine Concentrations in Intermediate Age-Related Macular Degeneration
title_sort plasma c-c chemokine concentrations in intermediate age-related macular degeneration
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636771/
https://www.ncbi.nlm.nih.gov/pubmed/34869411
http://dx.doi.org/10.3389/fmed.2021.710595
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