Chronic spontaneous urticaria: Evidence of systemic microcirculatory changes.

ELISA chronic spontaneous urticaria endothelial cell markers microcirculation videocapillaroscopy

Journal

Clinical and translational allergy
ISSN: 2045-7022
Titre abrégé: Clin Transl Allergy
Pays: England
ID NLM: 101576043

Informations de publication

Date de publication:
Jan 2024
Historique:
revised: 24 11 2023
received: 04 10 2023
accepted: 18 01 2024
medline: 29 1 2024
pubmed: 29 1 2024
entrez: 28 1 2024
Statut: ppublish

Résumé

Chronic spontaneous urticaria (CSU) is a chronic inflammatory skin disease where activation of endothelial cells (ECs) at sites of skin lesions leads to increased blood flow, leakage of fluid into the skin, cellular infiltration, and vascular remodeling. To understand the disease duration and the sometimes vague systemic symptoms accompanying flares, the objective of this study was to examine if CSU comes with systemic vascular changes at the microcirculatory level. We investigated CSU patients (n = 49) and healthy controls (HCs, n = 44) for microcirculatory differences by nailfold videocapillaroscopy (NVC) and for blood levels of the soluble EC biomarkers serum vascular endothelial growth factor (VEGF), soluble E-selectin, and stem cell factor (SCF). Patients were also assessed for clinical characteristics, disease activity, and markers of autoimmune CSU (aiCSU). CSU patients had significantly lower capillary density, more capillary malformations, and more irregular capillary dilations than HCs on NVC. Serum levels of VEGF, soluble E selectin and SCF were similar in CSU patients and HCs. CSU patients with higher VEGF levels had significantly more abnormal capillaries. Patients with markers of aiCSU, that is, low IgE levels or increased anti-TPO levels, had significantly more capillaries and less capillary dilations than those without. Our results suggest that CSU comes with systemic microcirculatory changes, which may be driven, in part, by VEGF.

Sections du résumé

BACKGROUND BACKGROUND
Chronic spontaneous urticaria (CSU) is a chronic inflammatory skin disease where activation of endothelial cells (ECs) at sites of skin lesions leads to increased blood flow, leakage of fluid into the skin, cellular infiltration, and vascular remodeling. To understand the disease duration and the sometimes vague systemic symptoms accompanying flares, the objective of this study was to examine if CSU comes with systemic vascular changes at the microcirculatory level.
METHODS METHODS
We investigated CSU patients (n = 49) and healthy controls (HCs, n = 44) for microcirculatory differences by nailfold videocapillaroscopy (NVC) and for blood levels of the soluble EC biomarkers serum vascular endothelial growth factor (VEGF), soluble E-selectin, and stem cell factor (SCF). Patients were also assessed for clinical characteristics, disease activity, and markers of autoimmune CSU (aiCSU).
RESULTS RESULTS
CSU patients had significantly lower capillary density, more capillary malformations, and more irregular capillary dilations than HCs on NVC. Serum levels of VEGF, soluble E selectin and SCF were similar in CSU patients and HCs. CSU patients with higher VEGF levels had significantly more abnormal capillaries. Patients with markers of aiCSU, that is, low IgE levels or increased anti-TPO levels, had significantly more capillaries and less capillary dilations than those without.
CONCLUSION CONCLUSIONS
Our results suggest that CSU comes with systemic microcirculatory changes, which may be driven, in part, by VEGF.

Identifiants

pubmed: 38282194
doi: 10.1002/clt2.12335
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e12335

Subventions

Organisme : The Brugmann Foundation

Informations de copyright

© 2024 The Authors. Clinical and Translational Allergy published by John Wiley & Sons Ltd on behalf of European Academy of Allergy and Clinical Immunology.

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Auteurs

Yora Mostmans (Y)

Department of Immunology-Allergology, CHU Brugmann, Université Libre de Bruxelles (ULB), Laken, Belgium.
Department of Dermatology, CHU Brugmann, ULB, Laken, Belgium.

Marcus Maurer (M)

Institute of Allergology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Allergology and Immunology, Berlin, Germany.

Bertrand Richert (B)

Department of Dermatology, CHU Brugmann, ULB, Laken, Belgium.

Vanessa Smith (V)

Department of Internal Medicine, Ghent University, Ghent, Belgium.
Department of Rheumatology, Ghent University Hospital, Ghent, Belgium.
Unit for Molecular Immunology and Inflammation, VIB Inflammation Research Center (IRC), Ghent, Belgium.

Karin Melsens (K)

Department of Internal Medicine, Ghent University, Ghent, Belgium.
Department of Rheumatology, Ghent University Hospital, Ghent, Belgium.
Unit for Molecular Immunology and Inflammation, VIB Inflammation Research Center (IRC), Ghent, Belgium.
Department of Rheumatology, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.

Viviane De Maertelaer (V)

IRIBHM, Statistical Unit, Fac. Medicine, ULB, Brussels, Belgium.

Ines Saidi (I)

Department of Dermatology, CHU Brugmann, ULB, Laken, Belgium.

Francis Corazza (F)

Department of Immunology, Laboratoire Hospitalier Universitaire de Bruxelles - Universitair Laboratorium Brussels (LHUB-ULB), Brussels, Belgium.

Olivier Michel (O)

Department of Immunology-Allergology, CHU Brugmann, Université Libre de Bruxelles (ULB), Laken, Belgium.

Classifications MeSH