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Enhanced Liver Fibrosis Score as a Biomarker for Vascular Damage Assessment in Patients with Takayasu Arteritis—A Pilot Study

Takayasu Arteritis (TA) is characterized by granulomatous panarteritis, vessel wall fibrosis, and irreversible vascular impairment. The aim of this study is to explore the usefulness of the Enhanced Liver Fibrosis score (ELF), procollagen-III aminoterminal propeptide (PIIINP), tissue inhibitor of ma...

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Autores principales: Stojanovic, Maja, Raskovic, Sanvila, Milivojevic, Vladimir, Miskovic, Rada, Soldatovic, Ivan, Stankovic, Sanja, Rankovic, Ivan, Stankovic Stanojevic, Marija, Dragasevic, Sanja, Krstic, Miodrag, Diamantopoulos, Andreas P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709028/
https://www.ncbi.nlm.nih.gov/pubmed/34940542
http://dx.doi.org/10.3390/jcdd8120187
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author Stojanovic, Maja
Raskovic, Sanvila
Milivojevic, Vladimir
Miskovic, Rada
Soldatovic, Ivan
Stankovic, Sanja
Rankovic, Ivan
Stankovic Stanojevic, Marija
Dragasevic, Sanja
Krstic, Miodrag
Diamantopoulos, Andreas P.
author_facet Stojanovic, Maja
Raskovic, Sanvila
Milivojevic, Vladimir
Miskovic, Rada
Soldatovic, Ivan
Stankovic, Sanja
Rankovic, Ivan
Stankovic Stanojevic, Marija
Dragasevic, Sanja
Krstic, Miodrag
Diamantopoulos, Andreas P.
author_sort Stojanovic, Maja
collection PubMed
description Takayasu Arteritis (TA) is characterized by granulomatous panarteritis, vessel wall fibrosis, and irreversible vascular impairment. The aim of this study is to explore the usefulness of the Enhanced Liver Fibrosis score (ELF), procollagen-III aminoterminal propeptide (PIIINP), tissue inhibitor of matrix metalloproteinase-1 (TIMP-1), and hyaluronic acid (HA) in assessing vascular damage in TA patients. ELF, PIIINP, TIMP-1, and HA were measured in 24 TA patients, and the results were correlated with the clinical damage indexes (VDI and TADS), an imaging damage score (CARDS), and disease activity scores (NIH and ITAS2010). A mean ELF score 8.42 (±1.12) and values higher than 7.7 (cut-off for liver fibrosis) in 21/24 (87.5%) of patients were detected. The VDI and TADS correlated significantly to ELF (p < 0.01). Additionally, a strong association across ELF and CARDS (p < 0.0001), PIIINP and CARDS (p < 0.001), and HA and CARDS (p < 0.001) was observed. No correlations of the tested biomarkers with inflammatory parameters, NIH, and ITAS2010 scores were found. To our knowledge, this is the first study that suggests the association of the serum biomarkers PIIINP, HA, and ELF score with damage but not with disease activity in TA patients. The ELF score and PIIINP may be useful biomarkers reflecting an ongoing fibrotic process and quantifying vascular damage.
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spelling pubmed-87090282021-12-25 Enhanced Liver Fibrosis Score as a Biomarker for Vascular Damage Assessment in Patients with Takayasu Arteritis—A Pilot Study Stojanovic, Maja Raskovic, Sanvila Milivojevic, Vladimir Miskovic, Rada Soldatovic, Ivan Stankovic, Sanja Rankovic, Ivan Stankovic Stanojevic, Marija Dragasevic, Sanja Krstic, Miodrag Diamantopoulos, Andreas P. J Cardiovasc Dev Dis Article Takayasu Arteritis (TA) is characterized by granulomatous panarteritis, vessel wall fibrosis, and irreversible vascular impairment. The aim of this study is to explore the usefulness of the Enhanced Liver Fibrosis score (ELF), procollagen-III aminoterminal propeptide (PIIINP), tissue inhibitor of matrix metalloproteinase-1 (TIMP-1), and hyaluronic acid (HA) in assessing vascular damage in TA patients. ELF, PIIINP, TIMP-1, and HA were measured in 24 TA patients, and the results were correlated with the clinical damage indexes (VDI and TADS), an imaging damage score (CARDS), and disease activity scores (NIH and ITAS2010). A mean ELF score 8.42 (±1.12) and values higher than 7.7 (cut-off for liver fibrosis) in 21/24 (87.5%) of patients were detected. The VDI and TADS correlated significantly to ELF (p < 0.01). Additionally, a strong association across ELF and CARDS (p < 0.0001), PIIINP and CARDS (p < 0.001), and HA and CARDS (p < 0.001) was observed. No correlations of the tested biomarkers with inflammatory parameters, NIH, and ITAS2010 scores were found. To our knowledge, this is the first study that suggests the association of the serum biomarkers PIIINP, HA, and ELF score with damage but not with disease activity in TA patients. The ELF score and PIIINP may be useful biomarkers reflecting an ongoing fibrotic process and quantifying vascular damage. MDPI 2021-12-14 /pmc/articles/PMC8709028/ /pubmed/34940542 http://dx.doi.org/10.3390/jcdd8120187 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Stojanovic, Maja
Raskovic, Sanvila
Milivojevic, Vladimir
Miskovic, Rada
Soldatovic, Ivan
Stankovic, Sanja
Rankovic, Ivan
Stankovic Stanojevic, Marija
Dragasevic, Sanja
Krstic, Miodrag
Diamantopoulos, Andreas P.
Enhanced Liver Fibrosis Score as a Biomarker for Vascular Damage Assessment in Patients with Takayasu Arteritis—A Pilot Study
title Enhanced Liver Fibrosis Score as a Biomarker for Vascular Damage Assessment in Patients with Takayasu Arteritis—A Pilot Study
title_full Enhanced Liver Fibrosis Score as a Biomarker for Vascular Damage Assessment in Patients with Takayasu Arteritis—A Pilot Study
title_fullStr Enhanced Liver Fibrosis Score as a Biomarker for Vascular Damage Assessment in Patients with Takayasu Arteritis—A Pilot Study
title_full_unstemmed Enhanced Liver Fibrosis Score as a Biomarker for Vascular Damage Assessment in Patients with Takayasu Arteritis—A Pilot Study
title_short Enhanced Liver Fibrosis Score as a Biomarker for Vascular Damage Assessment in Patients with Takayasu Arteritis—A Pilot Study
title_sort enhanced liver fibrosis score as a biomarker for vascular damage assessment in patients with takayasu arteritis—a pilot study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709028/
https://www.ncbi.nlm.nih.gov/pubmed/34940542
http://dx.doi.org/10.3390/jcdd8120187
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