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Pentraxin 3 Is a Predictor for Fibrosis and Arterial Stiffness in Patients with Nonalcoholic Fatty Liver Disease

Objective. The aim of the present study was to investigate whether pentraxin 3 (PTX3) can be a new noninvasive marker for prediction of liver fibrosis in patients with NAFLD. We also aimed to evaluate the relationship between PTX3 and atherosclerosis in patients with NAFLD. Method. Fifty-four male p...

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Autores principales: Ozturk, Kadir, Kurt, Omer, Dogan, Tolga, Ozen, Alptug, Demirci, Hakan, Yesildal, Fatih, Kantarcioglu, Murat, Turker, Turker, Guler, Ahmet Kerem, Karslioglu, Yıldırım, Altun, Battal, Uygun, Ahmet, Bagci, Sait
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779836/
https://www.ncbi.nlm.nih.gov/pubmed/26997950
http://dx.doi.org/10.1155/2016/1417962
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author Ozturk, Kadir
Kurt, Omer
Dogan, Tolga
Ozen, Alptug
Demirci, Hakan
Yesildal, Fatih
Kantarcioglu, Murat
Turker, Turker
Guler, Ahmet Kerem
Karslioglu, Yıldırım
Altun, Battal
Uygun, Ahmet
Bagci, Sait
author_facet Ozturk, Kadir
Kurt, Omer
Dogan, Tolga
Ozen, Alptug
Demirci, Hakan
Yesildal, Fatih
Kantarcioglu, Murat
Turker, Turker
Guler, Ahmet Kerem
Karslioglu, Yıldırım
Altun, Battal
Uygun, Ahmet
Bagci, Sait
author_sort Ozturk, Kadir
collection PubMed
description Objective. The aim of the present study was to investigate whether pentraxin 3 (PTX3) can be a new noninvasive marker for prediction of liver fibrosis in patients with NAFLD. We also aimed to evaluate the relationship between PTX3 and atherosclerosis in patients with NAFLD. Method. Fifty-four male patients with biopsy-proven NAFLD and 20 apparently healthy male volunteers were included. PTX3 levels were determined, using an ELISA method (R&D Sysytems, Quantikine ELISA, USA). To detect the presence of subclinical atherosclerosis in NAFLD, measurements of CIMT, FMD, and cf-PWV levels were performed. Results. PTX3 levels in NAFLD patients with fibrosis were higher than both NAFLD patients without fibrosis and controls (P = 0.032 and P = 0.028, respectively), but there was no difference between controls and NAFLD patients without fibrosis in terms of PTX3 levels (P = 0.903). PTX3 levels were strongly correlated with cf-PWV (r = 0.359, P = 0.003), whereas no significant correlation was found with other atherosclerosis markers, CIMT and FMD. Conclusion. Elevated plasma PTX3 levels are associated with the presence of fibrosis in patients with NAFLD, independently of metabolic syndrome components. This study demonstrated that for the first time there is a close association between elevated PTX3 levels and increased arterial stiffness in patients with NAFLD.
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spelling pubmed-47798362016-03-20 Pentraxin 3 Is a Predictor for Fibrosis and Arterial Stiffness in Patients with Nonalcoholic Fatty Liver Disease Ozturk, Kadir Kurt, Omer Dogan, Tolga Ozen, Alptug Demirci, Hakan Yesildal, Fatih Kantarcioglu, Murat Turker, Turker Guler, Ahmet Kerem Karslioglu, Yıldırım Altun, Battal Uygun, Ahmet Bagci, Sait Gastroenterol Res Pract Research Article Objective. The aim of the present study was to investigate whether pentraxin 3 (PTX3) can be a new noninvasive marker for prediction of liver fibrosis in patients with NAFLD. We also aimed to evaluate the relationship between PTX3 and atherosclerosis in patients with NAFLD. Method. Fifty-four male patients with biopsy-proven NAFLD and 20 apparently healthy male volunteers were included. PTX3 levels were determined, using an ELISA method (R&D Sysytems, Quantikine ELISA, USA). To detect the presence of subclinical atherosclerosis in NAFLD, measurements of CIMT, FMD, and cf-PWV levels were performed. Results. PTX3 levels in NAFLD patients with fibrosis were higher than both NAFLD patients without fibrosis and controls (P = 0.032 and P = 0.028, respectively), but there was no difference between controls and NAFLD patients without fibrosis in terms of PTX3 levels (P = 0.903). PTX3 levels were strongly correlated with cf-PWV (r = 0.359, P = 0.003), whereas no significant correlation was found with other atherosclerosis markers, CIMT and FMD. Conclusion. Elevated plasma PTX3 levels are associated with the presence of fibrosis in patients with NAFLD, independently of metabolic syndrome components. This study demonstrated that for the first time there is a close association between elevated PTX3 levels and increased arterial stiffness in patients with NAFLD. Hindawi Publishing Corporation 2016 2016-02-22 /pmc/articles/PMC4779836/ /pubmed/26997950 http://dx.doi.org/10.1155/2016/1417962 Text en Copyright © 2016 Kadir Ozturk 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
Ozturk, Kadir
Kurt, Omer
Dogan, Tolga
Ozen, Alptug
Demirci, Hakan
Yesildal, Fatih
Kantarcioglu, Murat
Turker, Turker
Guler, Ahmet Kerem
Karslioglu, Yıldırım
Altun, Battal
Uygun, Ahmet
Bagci, Sait
Pentraxin 3 Is a Predictor for Fibrosis and Arterial Stiffness in Patients with Nonalcoholic Fatty Liver Disease
title Pentraxin 3 Is a Predictor for Fibrosis and Arterial Stiffness in Patients with Nonalcoholic Fatty Liver Disease
title_full Pentraxin 3 Is a Predictor for Fibrosis and Arterial Stiffness in Patients with Nonalcoholic Fatty Liver Disease
title_fullStr Pentraxin 3 Is a Predictor for Fibrosis and Arterial Stiffness in Patients with Nonalcoholic Fatty Liver Disease
title_full_unstemmed Pentraxin 3 Is a Predictor for Fibrosis and Arterial Stiffness in Patients with Nonalcoholic Fatty Liver Disease
title_short Pentraxin 3 Is a Predictor for Fibrosis and Arterial Stiffness in Patients with Nonalcoholic Fatty Liver Disease
title_sort pentraxin 3 is a predictor for fibrosis and arterial stiffness in patients with nonalcoholic fatty liver disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779836/
https://www.ncbi.nlm.nih.gov/pubmed/26997950
http://dx.doi.org/10.1155/2016/1417962
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