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The Interplay Between Systemic Inflammatory Factors and MicroRNAs in Age-Related Macular Degeneration

We aimed to explore the expression of systemic inflammatory factors and selected intracellular miRNAs that regulate inflammatory signaling pathways potentially involved in age-related macular degeneration (AMD) pathogenesis. A total of 179 patients with wet AMD, 175 with dry AMD and 121 controls wer...

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Autores principales: Litwińska, Zofia, Sobuś, Anna, Łuczkowska, Karolina, Grabowicz, Aleksandra, Mozolewska-Piotrowska, Katarzyna, Safranow, Krzysztof, Kawa, Miłosz Piotr, Machaliński, Bogusław, Machalińska, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817913/
https://www.ncbi.nlm.nih.gov/pubmed/31695606
http://dx.doi.org/10.3389/fnagi.2019.00286
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author Litwińska, Zofia
Sobuś, Anna
Łuczkowska, Karolina
Grabowicz, Aleksandra
Mozolewska-Piotrowska, Katarzyna
Safranow, Krzysztof
Kawa, Miłosz Piotr
Machaliński, Bogusław
Machalińska, Anna
author_facet Litwińska, Zofia
Sobuś, Anna
Łuczkowska, Karolina
Grabowicz, Aleksandra
Mozolewska-Piotrowska, Katarzyna
Safranow, Krzysztof
Kawa, Miłosz Piotr
Machaliński, Bogusław
Machalińska, Anna
author_sort Litwińska, Zofia
collection PubMed
description We aimed to explore the expression of systemic inflammatory factors and selected intracellular miRNAs that regulate inflammatory signaling pathways potentially involved in age-related macular degeneration (AMD) pathogenesis. A total of 179 patients with wet AMD, 175 with dry AMD and 121 controls were enrolled in the study. Soluble inflammatory factors were analyzed in plasma samples using Luminex technology. Expression of selected miRNAs was analyzed in isolated nucleated peripheral blood cells (PBNCs) using real-time qPCR. Wet AMD was an independent factor associated with higher concentrations of IL-6 (β = +0.24, p = 0.0004), GM-CSF (β = +0.31, p < 0.001), IFN-γ (β = +0.58, p < 0.001), higher expression of miRNA-23a-3p (β = +0.60, p < 0.0001), miRNA-30b (β = +0.32, p < 0.0001), miRNA-191-5p (β = +0.28, p < 0.0001) and lower concentration of IL-1β (β = −0.25, p = 0.0003), IL-5 (β = −0.45, p < 0.001), IL-10 (β = −0.45, p < 0.001), IL-12 (β = −0.35, p < 0.001), lower expression of miRNA-16-5p (β = −0.31, p < 0.0001), miRNA-17-3p (β = −0.18, p = 0.01), miRNA-150-5p (β = −0.18, p = 0.01) and miRNA-155-5p (β = −0.47, p < 0.0001). Multivariate analysis revealed that dry AMD was an independent factor associated with higher concentration of GM-CSF (β = +0.34, p < 0.001), IL-6 (β = +0.13, p = 0.05), higher expression of miRNA-23a-3p (β = +0.60, p < 0.0001), miRNA-126-3p (β = +0.23, p = 0.0005), miRNA-126-5p (β = +0.16, p = 0.01), miRNA 146a (β = +0.14, p = 0.03), and mRNA191-5p (β = +0.15, p = 0.03) and lower concentrations of TNF-α (β = +0.24, p = 0.0004), IL-1β (β = −0.39, p < 0.001), IL-2 (β = −0.20, p = 0.003), IL-5 (β = −0.54, p < 0.001), IL-10 (β = −0.56, p < 0.001), IL-12 (β = −0.51, p < 0.001), lower expression of miRNA-16-5p (β = −0.23, p = 0.0004), miRNA-17-3p (β = −0.20, p = 0.003) and miRNA-17-5p (β = −0.19, p = 0.004). Negative correlations between visual acuity and WBC, lymphocyte count, TNF-α, IL-1 β, IL-2, IL-4, IL-6, IL-10 concentrations and miRNA-191-5p, as well as positive correlations between visual acuity and miRNA-126-3p, -126-5p, and -155-5p PBNCs expression were found in AMD patients. No such correlations were found in the control group. Our results may suggest the role of both intra- and extracellular mechanisms implicated in inflammatory response regulation in multifactorial AMD pathogenesis.
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spelling pubmed-68179132019-11-06 The Interplay Between Systemic Inflammatory Factors and MicroRNAs in Age-Related Macular Degeneration Litwińska, Zofia Sobuś, Anna Łuczkowska, Karolina Grabowicz, Aleksandra Mozolewska-Piotrowska, Katarzyna Safranow, Krzysztof Kawa, Miłosz Piotr Machaliński, Bogusław Machalińska, Anna Front Aging Neurosci Neuroscience We aimed to explore the expression of systemic inflammatory factors and selected intracellular miRNAs that regulate inflammatory signaling pathways potentially involved in age-related macular degeneration (AMD) pathogenesis. A total of 179 patients with wet AMD, 175 with dry AMD and 121 controls were enrolled in the study. Soluble inflammatory factors were analyzed in plasma samples using Luminex technology. Expression of selected miRNAs was analyzed in isolated nucleated peripheral blood cells (PBNCs) using real-time qPCR. Wet AMD was an independent factor associated with higher concentrations of IL-6 (β = +0.24, p = 0.0004), GM-CSF (β = +0.31, p < 0.001), IFN-γ (β = +0.58, p < 0.001), higher expression of miRNA-23a-3p (β = +0.60, p < 0.0001), miRNA-30b (β = +0.32, p < 0.0001), miRNA-191-5p (β = +0.28, p < 0.0001) and lower concentration of IL-1β (β = −0.25, p = 0.0003), IL-5 (β = −0.45, p < 0.001), IL-10 (β = −0.45, p < 0.001), IL-12 (β = −0.35, p < 0.001), lower expression of miRNA-16-5p (β = −0.31, p < 0.0001), miRNA-17-3p (β = −0.18, p = 0.01), miRNA-150-5p (β = −0.18, p = 0.01) and miRNA-155-5p (β = −0.47, p < 0.0001). Multivariate analysis revealed that dry AMD was an independent factor associated with higher concentration of GM-CSF (β = +0.34, p < 0.001), IL-6 (β = +0.13, p = 0.05), higher expression of miRNA-23a-3p (β = +0.60, p < 0.0001), miRNA-126-3p (β = +0.23, p = 0.0005), miRNA-126-5p (β = +0.16, p = 0.01), miRNA 146a (β = +0.14, p = 0.03), and mRNA191-5p (β = +0.15, p = 0.03) and lower concentrations of TNF-α (β = +0.24, p = 0.0004), IL-1β (β = −0.39, p < 0.001), IL-2 (β = −0.20, p = 0.003), IL-5 (β = −0.54, p < 0.001), IL-10 (β = −0.56, p < 0.001), IL-12 (β = −0.51, p < 0.001), lower expression of miRNA-16-5p (β = −0.23, p = 0.0004), miRNA-17-3p (β = −0.20, p = 0.003) and miRNA-17-5p (β = −0.19, p = 0.004). Negative correlations between visual acuity and WBC, lymphocyte count, TNF-α, IL-1 β, IL-2, IL-4, IL-6, IL-10 concentrations and miRNA-191-5p, as well as positive correlations between visual acuity and miRNA-126-3p, -126-5p, and -155-5p PBNCs expression were found in AMD patients. No such correlations were found in the control group. Our results may suggest the role of both intra- and extracellular mechanisms implicated in inflammatory response regulation in multifactorial AMD pathogenesis. Frontiers Media S.A. 2019-10-22 /pmc/articles/PMC6817913/ /pubmed/31695606 http://dx.doi.org/10.3389/fnagi.2019.00286 Text en Copyright © 2019 Litwińska, Sobuś, Łuczkowska, Grabowicz, Mozolewska-Piotrowska, Safranow, Kawa, Machaliński and Machalińska. http://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 Neuroscience
Litwińska, Zofia
Sobuś, Anna
Łuczkowska, Karolina
Grabowicz, Aleksandra
Mozolewska-Piotrowska, Katarzyna
Safranow, Krzysztof
Kawa, Miłosz Piotr
Machaliński, Bogusław
Machalińska, Anna
The Interplay Between Systemic Inflammatory Factors and MicroRNAs in Age-Related Macular Degeneration
title The Interplay Between Systemic Inflammatory Factors and MicroRNAs in Age-Related Macular Degeneration
title_full The Interplay Between Systemic Inflammatory Factors and MicroRNAs in Age-Related Macular Degeneration
title_fullStr The Interplay Between Systemic Inflammatory Factors and MicroRNAs in Age-Related Macular Degeneration
title_full_unstemmed The Interplay Between Systemic Inflammatory Factors and MicroRNAs in Age-Related Macular Degeneration
title_short The Interplay Between Systemic Inflammatory Factors and MicroRNAs in Age-Related Macular Degeneration
title_sort interplay between systemic inflammatory factors and micrornas in age-related macular degeneration
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817913/
https://www.ncbi.nlm.nih.gov/pubmed/31695606
http://dx.doi.org/10.3389/fnagi.2019.00286
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