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Association of Haemostatic and Inflammatory Biomarkers with Nephropathy in Type 1 Diabetes Mellitus

This study aimed at investigating the association between haemostatic biomarkers, proinflammatory, and anti-inflammatory cytokines with chronic kidney disease in type 1 diabetic patients. Patients were divided into two groups: with nephropathy (albuminuria ≥ 30 mg/g and/or GFR < 60 mL/min/1.73 m(...

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Autores principales: Domingueti, Caroline Pereira, Fóscolo, Rodrigo Bastos, Reis, Janice Sepúlveda, Campos, Fernanda Magalhães Freire, Dusse, Luci Maria S., Carvalho, Maria das Graças, Braga Gomes, Karina, Fernandes, Ana Paula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684869/
https://www.ncbi.nlm.nih.gov/pubmed/26770985
http://dx.doi.org/10.1155/2016/2315260
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author Domingueti, Caroline Pereira
Fóscolo, Rodrigo Bastos
Reis, Janice Sepúlveda
Campos, Fernanda Magalhães Freire
Dusse, Luci Maria S.
Carvalho, Maria das Graças
Braga Gomes, Karina
Fernandes, Ana Paula
author_facet Domingueti, Caroline Pereira
Fóscolo, Rodrigo Bastos
Reis, Janice Sepúlveda
Campos, Fernanda Magalhães Freire
Dusse, Luci Maria S.
Carvalho, Maria das Graças
Braga Gomes, Karina
Fernandes, Ana Paula
author_sort Domingueti, Caroline Pereira
collection PubMed
description This study aimed at investigating the association between haemostatic biomarkers, proinflammatory, and anti-inflammatory cytokines with chronic kidney disease in type 1 diabetic patients. Patients were divided into two groups: with nephropathy (albuminuria ≥ 30 mg/g and/or GFR < 60 mL/min/1.73 m(2)), n = 65; and without nephropathy (albuminuria < 30 mg/g and GFR ≥ 60 mL/min/1.73 m(2)), n = 60. INF-γ, IL-6, IL-10, and TNF-α plasma levels were determined by flow cytometry. VWF, ADAMTS13 antigen, and D-Dimer plasma levels were determined by enzyme-linked immunosorbent assay and ADAMTS13 activity was assessed by fluorescence resonance energy transfer assay. Elevated levels of INF-γ, VWF, ADAMTS13 antigen, D-Dimer, and reduced ADAMTS13 activity/antigen ratio were observed in patients with nephropathy as compared to those without nephropathy (P = 0.001, P < 0.001, P < 0.001, P < 0.001, and P < 0.001, resp.). Cytokines and haemostatic biomarkers remained associated with nephropathy after adjustments (use of statin, acetylsalicylic acid, angiotensin converting enzyme inhibitor, and angiotensin antagonist). INF-γ, TNF-α, and IL-10 significantly correlated with haemostatic biomarkers. Inflammatory and hypercoagulability status are associated with nephropathy in type 1 diabetes mellitus and an interrelationship between them may play an important role in pathogenesis of diabetic nephropathy.
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spelling pubmed-46848692016-01-14 Association of Haemostatic and Inflammatory Biomarkers with Nephropathy in Type 1 Diabetes Mellitus Domingueti, Caroline Pereira Fóscolo, Rodrigo Bastos Reis, Janice Sepúlveda Campos, Fernanda Magalhães Freire Dusse, Luci Maria S. Carvalho, Maria das Graças Braga Gomes, Karina Fernandes, Ana Paula J Diabetes Res Research Article This study aimed at investigating the association between haemostatic biomarkers, proinflammatory, and anti-inflammatory cytokines with chronic kidney disease in type 1 diabetic patients. Patients were divided into two groups: with nephropathy (albuminuria ≥ 30 mg/g and/or GFR < 60 mL/min/1.73 m(2)), n = 65; and without nephropathy (albuminuria < 30 mg/g and GFR ≥ 60 mL/min/1.73 m(2)), n = 60. INF-γ, IL-6, IL-10, and TNF-α plasma levels were determined by flow cytometry. VWF, ADAMTS13 antigen, and D-Dimer plasma levels were determined by enzyme-linked immunosorbent assay and ADAMTS13 activity was assessed by fluorescence resonance energy transfer assay. Elevated levels of INF-γ, VWF, ADAMTS13 antigen, D-Dimer, and reduced ADAMTS13 activity/antigen ratio were observed in patients with nephropathy as compared to those without nephropathy (P = 0.001, P < 0.001, P < 0.001, P < 0.001, and P < 0.001, resp.). Cytokines and haemostatic biomarkers remained associated with nephropathy after adjustments (use of statin, acetylsalicylic acid, angiotensin converting enzyme inhibitor, and angiotensin antagonist). INF-γ, TNF-α, and IL-10 significantly correlated with haemostatic biomarkers. Inflammatory and hypercoagulability status are associated with nephropathy in type 1 diabetes mellitus and an interrelationship between them may play an important role in pathogenesis of diabetic nephropathy. Hindawi Publishing Corporation 2016 2015-12-06 /pmc/articles/PMC4684869/ /pubmed/26770985 http://dx.doi.org/10.1155/2016/2315260 Text en Copyright © 2016 Caroline Pereira Domingueti et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Domingueti, Caroline Pereira
Fóscolo, Rodrigo Bastos
Reis, Janice Sepúlveda
Campos, Fernanda Magalhães Freire
Dusse, Luci Maria S.
Carvalho, Maria das Graças
Braga Gomes, Karina
Fernandes, Ana Paula
Association of Haemostatic and Inflammatory Biomarkers with Nephropathy in Type 1 Diabetes Mellitus
title Association of Haemostatic and Inflammatory Biomarkers with Nephropathy in Type 1 Diabetes Mellitus
title_full Association of Haemostatic and Inflammatory Biomarkers with Nephropathy in Type 1 Diabetes Mellitus
title_fullStr Association of Haemostatic and Inflammatory Biomarkers with Nephropathy in Type 1 Diabetes Mellitus
title_full_unstemmed Association of Haemostatic and Inflammatory Biomarkers with Nephropathy in Type 1 Diabetes Mellitus
title_short Association of Haemostatic and Inflammatory Biomarkers with Nephropathy in Type 1 Diabetes Mellitus
title_sort association of haemostatic and inflammatory biomarkers with nephropathy in type 1 diabetes mellitus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684869/
https://www.ncbi.nlm.nih.gov/pubmed/26770985
http://dx.doi.org/10.1155/2016/2315260
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