Blood Adhesion Molecules as Biomarkers in Children with Chronic Urticaria
- PMID: 38671667
- PMCID: PMC11048842
- DOI: 10.3390/children11040449
Blood Adhesion Molecules as Biomarkers in Children with Chronic Urticaria
Abstract
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: 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: 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 (p = 0.03 and p = 0.01, respectively) following treatment. Similarly, the acute urticaria group exhibited significant reduction in the mean levels of VCAM and ICAM (p < 0.001). In both groups, the mean level of ICAM after treatment was comparable with that of the comparison group.
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.
Keywords: acute urticaria; childhood; chronic urticaria; intercellular adhesion molecule 1; vascular cell adhesion molecule 1.
Conflict of interest statement
The authors declare no conflicts of interest.
Figures



Similar articles
-
Plasma soluble adhesion molecules; intercellular adhesion molecule-1, vascular cell adhesion molecule-1 and E-selectin levels in patients with isolated coronary artery ectasia.Coron Artery Dis. 2005 Feb;16(1):45-50. doi: 10.1097/00019501-200502000-00009. Coron Artery Dis. 2005. PMID: 15654200
-
Rabbit vascular endothelial adhesion molecules: ELAM-1 is most elevated in acute inflammation, whereas VCAM-1 and ICAM-1 predominate in chronic inflammation.J Leukoc Biol. 1996 Dec;60(6):692-703. doi: 10.1002/jlb.60.6.692. J Leukoc Biol. 1996. PMID: 8975870
-
Precise ultrastructural localization of endothelial leukocyte adhesion molecule-1, vascular cell adhesion molecule-1, and intercellular adhesion molecule-1 in patients with IgA nephropathy.Nephron. 1997;75(1):54-64. doi: 10.1159/000189500. Nephron. 1997. PMID: 9031271
-
Effect of Endothelial Adhesion Molecules on Atrial Fibrillation: A Systematic Review and Meta-analysis.Heart Int. 2022 Aug 31;16(2):75-84. doi: 10.17925/HI.2022.16.2.75. eCollection 2022. Heart Int. 2022. PMID: 36741104 Free PMC article. Review.
-
Effects of Nigella sativa on VCAM-1 and ICAM-1: A systematic review of preclinical and clinical studies.J Cardiovasc Thorac Res. 2025 Mar 18;17(1):12-19. doi: 10.34172/jcvtr.025.33343. eCollection 2025 Mar. J Cardiovasc Thorac Res. 2025. PMID: 40365513 Free PMC article. Review.
References
-
- Zuberbier T., Aberer W., Asero R., Abdul Latiff A.H., Baker D., Ballmer-Weber B., Bernstein J.A., Bindslev-Jensen C., Brzoza Z., Buense Bedrikow R., et al. The EAACI/GA2LEN/EDF/WAO Guideline for the definition, classification, diagnosis, and management of urticaria. Allergy. 2018;73:1393–1414. doi: 10.1111/all.13397. - DOI - PubMed
LinkOut - more resources
Full Text Sources
Miscellaneous