Serum Vascular Adhesion Protein-1 and Endothelial Dysfunction in Hepatic Cirrhosis: Searching for New Prognostic Markers.
Humans
Male
Liver Cirrhosis
/ blood
Female
Middle Aged
Biomarkers
/ blood
Vascular Cell Adhesion Molecule-1
/ blood
Prognosis
Carcinoma, Hepatocellular
/ blood
Aged
Amine Oxidase (Copper-Containing)
/ blood
Liver Neoplasms
/ blood
Cross-Sectional Studies
Intercellular Adhesion Molecule-1
/ blood
Endothelium, Vascular
/ metabolism
Adult
Tumor Necrosis Factor-alpha
/ blood
Cytokines
/ blood
Cell Adhesion Molecules
adhesion molecules
alcoholic cirrhosis
endothelial dysfunction
hepatocellular carcinoma
vascular adhesion protein-1
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
03 Jul 2024
03 Jul 2024
Historique:
received:
08
05
2024
revised:
28
06
2024
accepted:
28
06
2024
medline:
13
7
2024
pubmed:
13
7
2024
entrez:
13
7
2024
Statut:
epublish
Résumé
Endothelial dysfunction plays a key role in the development of liver cirrhosis. Among the biomarkers of endothelial dysfunction, the soluble form of Vascular Adhesion Protein-1 (sVAP-1) is an unconventional and less known adhesion molecule endowed also with amine oxidase activity. The aim of this study was to explore and correlate the behavior of sVAP-1 with that of the soluble vascular cell adhesion molecule-1 (sVCAM-1) and intercellular adhesion molecule-1 (sICAM-1) and with the severity of liver cirrhosis. A cross-sectional study was carried out by enrolling 28 controls, 59 cirrhotic patients without hepatocellular carcinoma, and 56 patients with hepatocellular carcinoma (HCC), mainly caused by alcohol abuse. The levels of adhesion molecules and of the pro-inflammatory cytokines (IL-6 and TNF-αα) were determined by immunoassay and the enzymatic activity of sVAP-1 by a fluorometric assay. In non-diabetic patients without HCC, a specific behavior of sVAP-1 was highlighted. Differently from sVCAM-1, sICAM-1, and cytokines, the sVAP-1 level was significantly increased only in the early stage of disease, and then, it decreased in the last stage (866 ± 390 ng/mL vs. 545 ± 316 ng/mL, in Child-Pugh class A vs. C, respectively,
Identifiants
pubmed: 39000418
pii: ijms25137309
doi: 10.3390/ijms25137309
pii:
doi:
Substances chimiques
Biomarkers
0
Vascular Cell Adhesion Molecule-1
0
AOC3 protein, human
EC 1.4.3.21
Amine Oxidase (Copper-Containing)
EC 1.4.3.21
Intercellular Adhesion Molecule-1
126547-89-5
Tumor Necrosis Factor-alpha
0
Cytokines
0
Cell Adhesion Molecules
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM