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Interleukin-8 is increased in chronic kidney disease in children, but not related to cardiovascular disease

INTRODUCTION: In this study, we aimed to detect the cytokine that is involved in the early stage of chronic kidney disease and associated with cardiovascular disease. METHODS: We included 50 patients who were diagnosed with predialytic chronic kidney disease and 30 healthy pediatric patients in Ege...

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Autores principales: Tunçay, Seçil Conkar, Doğan, Eser, Hakverdi, Gülden, Tutar, Zulal Ülger, Mir, Sevgi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Nefrologia 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8428641/
https://www.ncbi.nlm.nih.gov/pubmed/33711092
http://dx.doi.org/10.1590/2175-8239-JBN-2020-0225
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author Tunçay, Seçil Conkar
Doğan, Eser
Hakverdi, Gülden
Tutar, Zulal Ülger
Mir, Sevgi
author_facet Tunçay, Seçil Conkar
Doğan, Eser
Hakverdi, Gülden
Tutar, Zulal Ülger
Mir, Sevgi
author_sort Tunçay, Seçil Conkar
collection PubMed
description INTRODUCTION: In this study, we aimed to detect the cytokine that is involved in the early stage of chronic kidney disease and associated with cardiovascular disease. METHODS: We included 50 patients who were diagnosed with predialytic chronic kidney disease and 30 healthy pediatric patients in Ege University Medical Faculty Pediatric Clinic, İzmir/Turkey. Interleukin-8 (IL-8), interleukin-10 (IL-10), interleukin-13 (IL-13), and transforming grow factor-β1 (TGF-β1) levels (pg/mL) were measured by ELISA. Carotid-femoral pulse wave velocity (PWV), augmentation index (Aix), carotid intima media thickness (cIMT), and left ventricular mass index (LVMI) were evaluated as markers of cardiovascular disease. The presence of a cardiovascular disease marker was defined as an abnormality in any of the parameters (cIMT, PWV, Aix, and left ventricular mass index (SVKI)). The patient group was divided into two groups as with and without cardiovascular disease. RESULTS: Mean Aix and PWV values were higher in CKD patients than controls (Aix: CKD 32.8±11.11%, healthy subjects: 6.74±6.58%, PWV CKD: 7.31±4.34m/s, healthy subjects: 3.42±3.01m/s, respectively; p=0.02, p=0.03). The serum IL-8 levels of CKD were significantly higher than of healthy subjects 568.48±487.35pg/mL, 33.67±47.47pg/mL, respectively (p<0.001). There was no statistically significant difference between IL-8, IL-10, IL-13, TGF-1, in CKD patients with and without cardiovascular disease (p> 0.05). DISCUSSION: IL-8 is the sole cytokine that increases in pediatric patients with chronic kidney disease among other cytokines (IL-10, IL-13 and TGF-β1). However, we did not show that IL-8 is related to the presence of cardiovascular disease.
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spelling pubmed-84286412021-09-16 Interleukin-8 is increased in chronic kidney disease in children, but not related to cardiovascular disease Tunçay, Seçil Conkar Doğan, Eser Hakverdi, Gülden Tutar, Zulal Ülger Mir, Sevgi J Bras Nefrol Original Article INTRODUCTION: In this study, we aimed to detect the cytokine that is involved in the early stage of chronic kidney disease and associated with cardiovascular disease. METHODS: We included 50 patients who were diagnosed with predialytic chronic kidney disease and 30 healthy pediatric patients in Ege University Medical Faculty Pediatric Clinic, İzmir/Turkey. Interleukin-8 (IL-8), interleukin-10 (IL-10), interleukin-13 (IL-13), and transforming grow factor-β1 (TGF-β1) levels (pg/mL) were measured by ELISA. Carotid-femoral pulse wave velocity (PWV), augmentation index (Aix), carotid intima media thickness (cIMT), and left ventricular mass index (LVMI) were evaluated as markers of cardiovascular disease. The presence of a cardiovascular disease marker was defined as an abnormality in any of the parameters (cIMT, PWV, Aix, and left ventricular mass index (SVKI)). The patient group was divided into two groups as with and without cardiovascular disease. RESULTS: Mean Aix and PWV values were higher in CKD patients than controls (Aix: CKD 32.8±11.11%, healthy subjects: 6.74±6.58%, PWV CKD: 7.31±4.34m/s, healthy subjects: 3.42±3.01m/s, respectively; p=0.02, p=0.03). The serum IL-8 levels of CKD were significantly higher than of healthy subjects 568.48±487.35pg/mL, 33.67±47.47pg/mL, respectively (p<0.001). There was no statistically significant difference between IL-8, IL-10, IL-13, TGF-1, in CKD patients with and without cardiovascular disease (p> 0.05). DISCUSSION: IL-8 is the sole cytokine that increases in pediatric patients with chronic kidney disease among other cytokines (IL-10, IL-13 and TGF-β1). However, we did not show that IL-8 is related to the presence of cardiovascular disease. Sociedade Brasileira de Nefrologia 2021-03-12 2021 /pmc/articles/PMC8428641/ /pubmed/33711092 http://dx.doi.org/10.1590/2175-8239-JBN-2020-0225 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Tunçay, Seçil Conkar
Doğan, Eser
Hakverdi, Gülden
Tutar, Zulal Ülger
Mir, Sevgi
Interleukin-8 is increased in chronic kidney disease in children, but not related to cardiovascular disease
title Interleukin-8 is increased in chronic kidney disease in children, but not related to cardiovascular disease
title_full Interleukin-8 is increased in chronic kidney disease in children, but not related to cardiovascular disease
title_fullStr Interleukin-8 is increased in chronic kidney disease in children, but not related to cardiovascular disease
title_full_unstemmed Interleukin-8 is increased in chronic kidney disease in children, but not related to cardiovascular disease
title_short Interleukin-8 is increased in chronic kidney disease in children, but not related to cardiovascular disease
title_sort interleukin-8 is increased in chronic kidney disease in children, but not related to cardiovascular disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8428641/
https://www.ncbi.nlm.nih.gov/pubmed/33711092
http://dx.doi.org/10.1590/2175-8239-JBN-2020-0225
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