Cargando…

Circulating Profile of ECM-Related Proteins as Diagnostic Markers in Inflammatory Bowel Diseases

The aim of our research was to find new biomarkers that could be potentially used in the diagnosis, differentiation and monitoring of inflammatory bowel diseases (IBD). Since extracellular matrix (ECM) remodeling contributes to the pathological changes occurring in IBD, the serum profile of ECM-rela...

Descripción completa

Detalles Bibliográficos
Autores principales: Komosinska-Vassev, Katarzyna, Kałużna, Aleksandra, Jura-Półtorak, Agnieszka, Derkacz, Alicja, Olczyk, Krystyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570505/
https://www.ncbi.nlm.nih.gov/pubmed/36233486
http://dx.doi.org/10.3390/jcm11195618
_version_ 1784810126378532864
author Komosinska-Vassev, Katarzyna
Kałużna, Aleksandra
Jura-Półtorak, Agnieszka
Derkacz, Alicja
Olczyk, Krystyna
author_facet Komosinska-Vassev, Katarzyna
Kałużna, Aleksandra
Jura-Półtorak, Agnieszka
Derkacz, Alicja
Olczyk, Krystyna
author_sort Komosinska-Vassev, Katarzyna
collection PubMed
description The aim of our research was to find new biomarkers that could be potentially used in the diagnosis, differentiation and monitoring of inflammatory bowel diseases (IBD). Since extracellular matrix (ECM) remodeling contributes to the pathological changes occurring in IBD, the serum profile of ECM-related proteins may reflect disease activity in the intestinal mucosa. Serum laminin (LM), fibronectin (FN) and gelatinase-associated lipocalin (NGAL) concentrations were determined in 51 patients with IBD before and after a year of treatment, as well as in 48 healthy individuals. A significant difference in serum concentration of FN (130,56 ± 52.87 vs. 287.93 ± 79.69, p < 0.001) and NGAL (133.34 ± 51.51 vs. 102.37.39, p < 0.05) between patients with ulcerative colitis (UC) and healthy individuals was found. In patients with Crohn’s disease (CD), serum concentrations of LM (1329.5 ± 389.36 vs. 1012.07 ± 260.85, p < 0.005) and NGAL (138.94 ± 51.31 vs. 102.65 ± 37.39, p < 0.05) were increased, while FN (89.26 ± 43.86 vs. 287.93 ± 79.69, p < 0.001) was decreased compared to healthy subjects. Moreover, a significant correlation was found between the Mayo score in patients with UC and the levels of NGAL (r = 0.49, p < 0.01) and LM (r = 0.035, p < 0.005), respectively. Another significant correlation was noted between the Crohn’s Disease Activity Index (CDAI) and LM (r = 0.49, p < 0.05) levels in CD group. The results presented in our studies indicate that ECM-related markers might be potential additional tools helpful in diagnosing IBD, differential diagnosis of UC and CD and monitoring the disease activity.
format Online
Article
Text
id pubmed-9570505
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-95705052022-10-17 Circulating Profile of ECM-Related Proteins as Diagnostic Markers in Inflammatory Bowel Diseases Komosinska-Vassev, Katarzyna Kałużna, Aleksandra Jura-Półtorak, Agnieszka Derkacz, Alicja Olczyk, Krystyna J Clin Med Article The aim of our research was to find new biomarkers that could be potentially used in the diagnosis, differentiation and monitoring of inflammatory bowel diseases (IBD). Since extracellular matrix (ECM) remodeling contributes to the pathological changes occurring in IBD, the serum profile of ECM-related proteins may reflect disease activity in the intestinal mucosa. Serum laminin (LM), fibronectin (FN) and gelatinase-associated lipocalin (NGAL) concentrations were determined in 51 patients with IBD before and after a year of treatment, as well as in 48 healthy individuals. A significant difference in serum concentration of FN (130,56 ± 52.87 vs. 287.93 ± 79.69, p < 0.001) and NGAL (133.34 ± 51.51 vs. 102.37.39, p < 0.05) between patients with ulcerative colitis (UC) and healthy individuals was found. In patients with Crohn’s disease (CD), serum concentrations of LM (1329.5 ± 389.36 vs. 1012.07 ± 260.85, p < 0.005) and NGAL (138.94 ± 51.31 vs. 102.65 ± 37.39, p < 0.05) were increased, while FN (89.26 ± 43.86 vs. 287.93 ± 79.69, p < 0.001) was decreased compared to healthy subjects. Moreover, a significant correlation was found between the Mayo score in patients with UC and the levels of NGAL (r = 0.49, p < 0.01) and LM (r = 0.035, p < 0.005), respectively. Another significant correlation was noted between the Crohn’s Disease Activity Index (CDAI) and LM (r = 0.49, p < 0.05) levels in CD group. The results presented in our studies indicate that ECM-related markers might be potential additional tools helpful in diagnosing IBD, differential diagnosis of UC and CD and monitoring the disease activity. MDPI 2022-09-23 /pmc/articles/PMC9570505/ /pubmed/36233486 http://dx.doi.org/10.3390/jcm11195618 Text en © 2022 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
Komosinska-Vassev, Katarzyna
Kałużna, Aleksandra
Jura-Półtorak, Agnieszka
Derkacz, Alicja
Olczyk, Krystyna
Circulating Profile of ECM-Related Proteins as Diagnostic Markers in Inflammatory Bowel Diseases
title Circulating Profile of ECM-Related Proteins as Diagnostic Markers in Inflammatory Bowel Diseases
title_full Circulating Profile of ECM-Related Proteins as Diagnostic Markers in Inflammatory Bowel Diseases
title_fullStr Circulating Profile of ECM-Related Proteins as Diagnostic Markers in Inflammatory Bowel Diseases
title_full_unstemmed Circulating Profile of ECM-Related Proteins as Diagnostic Markers in Inflammatory Bowel Diseases
title_short Circulating Profile of ECM-Related Proteins as Diagnostic Markers in Inflammatory Bowel Diseases
title_sort circulating profile of ecm-related proteins as diagnostic markers in inflammatory bowel diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570505/
https://www.ncbi.nlm.nih.gov/pubmed/36233486
http://dx.doi.org/10.3390/jcm11195618
work_keys_str_mv AT komosinskavassevkatarzyna circulatingprofileofecmrelatedproteinsasdiagnosticmarkersininflammatoryboweldiseases
AT kałuznaaleksandra circulatingprofileofecmrelatedproteinsasdiagnosticmarkersininflammatoryboweldiseases
AT jurapołtorakagnieszka circulatingprofileofecmrelatedproteinsasdiagnosticmarkersininflammatoryboweldiseases
AT derkaczalicja circulatingprofileofecmrelatedproteinsasdiagnosticmarkersininflammatoryboweldiseases
AT olczykkrystyna circulatingprofileofecmrelatedproteinsasdiagnosticmarkersininflammatoryboweldiseases