Blood Adhesion Molecules as Biomarkers in Children with Chronic Urticaria.

acute urticaria childhood chronic urticaria intercellular adhesion molecule 1 vascular cell adhesion molecule 1

Journal

Children (Basel, Switzerland)
ISSN: 2227-9067
Titre abrégé: Children (Basel)
Pays: Switzerland
ID NLM: 101648936

Informations de publication

Date de publication:
08 Apr 2024
Historique:
received: 30 12 2023
revised: 18 02 2024
accepted: 26 03 2024
medline: 27 4 2024
pubmed: 27 4 2024
entrez: 27 4 2024
Statut: epublish

Résumé

The prevailing etiological model of both acute and chronic urticaria implicates specific allergen exposure that triggers the local release of vasoactive factors and inflammatory adhesion molecules, including vascular cell adhesion molecule 1 (VCAM-1), intercellular adhesion molecule 1 (ICAM-1), endothelial leukocyte adhesion molecule 1 (ELAM-1), P-selectin and E-selectin in the superficial dermis. This study focused on the possible role of VCAM-1 and ICAM-1 as biomarkers in children with acute and chronic urticaria. This study involved 184 children, 40 with acute urticaria, 71 with chronic urticaria, and 73 matched comparison subjects. The serum levels of ICAM-1 and VCAM-1 were determined in venous blood in all the participants on enrollment. Antihistamine treatment was administered to all the patients. In the children with chronic urticaria, the Urticaria Activity Score Questionnaire (UAS7) was completed daily by the parents. In 16 of the patients with acute urticaria and 43 with chronic urticaria, the serum levels of ICAM-1 and VCAM-1 were determined at follow-up after 6-8 weeks of treatment. The mean serum levels of both VCAM-1 and ICAM-1 were higher in both groups of children with urticaria than in the comparison subjects at the start of the study. In the chronic urticaria group, the levels decreased significantly ( VCAM-1 and ICAM-1 are suggested as promising biomarkers for monitoring both acute and chronic urticaria in children. Future research should explore their utility in larger cohorts and investigate their role in personalized treatment strategies.

Sections du résumé

BACKGROUND BACKGROUND
The prevailing etiological model of both acute and chronic urticaria implicates specific allergen exposure that triggers the local release of vasoactive factors and inflammatory adhesion molecules, including vascular cell adhesion molecule 1 (VCAM-1), intercellular adhesion molecule 1 (ICAM-1), endothelial leukocyte adhesion molecule 1 (ELAM-1), P-selectin and E-selectin in the superficial dermis. This study focused on the possible role of VCAM-1 and ICAM-1 as biomarkers in children with acute and chronic urticaria.
METHODS METHODS
This study involved 184 children, 40 with acute urticaria, 71 with chronic urticaria, and 73 matched comparison subjects. The serum levels of ICAM-1 and VCAM-1 were determined in venous blood in all the participants on enrollment. Antihistamine treatment was administered to all the patients. In the children with chronic urticaria, the Urticaria Activity Score Questionnaire (UAS7) was completed daily by the parents. In 16 of the patients with acute urticaria and 43 with chronic urticaria, the serum levels of ICAM-1 and VCAM-1 were determined at follow-up after 6-8 weeks of treatment.
RESULTS RESULTS
The mean serum levels of both VCAM-1 and ICAM-1 were higher in both groups of children with urticaria than in the comparison subjects at the start of the study. In the chronic urticaria group, the levels decreased significantly (
CONCLUSIONS CONCLUSIONS
VCAM-1 and ICAM-1 are suggested as promising biomarkers for monitoring both acute and chronic urticaria in children. Future research should explore their utility in larger cohorts and investigate their role in personalized treatment strategies.

Identifiants

pubmed: 38671667
pii: children11040449
doi: 10.3390/children11040449
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Ioanna Angeli (I)

Department of Pediatrics, School of Medicine, University of Ioannina, 45332 Ioannina, Greece.

Emilia Vassilopoulou (E)

Pediatric Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.

Dimitrios Cassimos (D)

Pediatric Department, Democritus University of Thrace, 68100 Alexandroupolis, Greece.

Ioannis Fotopoulos (I)

Department of Computer Science, University of Crete, Voutes Campus, 70013 Heraklion, Greece.

Anastasios Serbis (A)

Department of Pediatrics, School of Medicine, University of Ioannina, 45332 Ioannina, Greece.

Makis Alexandros (M)

Department of Pediatrics, School of Medicine, University of Ioannina, 45332 Ioannina, Greece.

Sophia Tsabouri (S)

Department of Pediatrics, School of Medicine, University of Ioannina, 45332 Ioannina, Greece.

Classifications MeSH