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...
Autores principales: | , , , , |
---|---|
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 |