Evidence for neurogenic inflammation in lichen planopilaris and frontal fibrosing alopecia pathogenic mechanism.


Journal

Experimental dermatology
ISSN: 1600-0625
Titre abrégé: Exp Dermatol
Pays: Denmark
ID NLM: 9301549

Informations de publication

Date de publication:
03 2020
Historique:
received: 04 04 2018
revised: 17 10 2018
accepted: 01 11 2018
pubmed: 9 11 2018
medline: 28 9 2021
entrez: 9 11 2018
Statut: ppublish

Résumé

Lichen planopilaris (LPP) and frontal fibrosing alopecia (FFA) are lymphocytic scarring alopecias affecting primarily the scalp. Although both diseases may share some clinical and histopathological features, in the last decade, FFA has become an "epidemic" particularly in Europe, North and South America with unique clinical manifestations compared to LPP, thus, raising the idea that this disease may have a different pathogenesis. Symptoms such as scalp burning, pruritus or pain are usually present in both diseases, suggesting a possible role for nerves and neuropeptides in the pathogenesis of both diseases. Based on some previous studies, neuropeptides, such as substance P (SP) and calcitonin gene-related peptide (CGRP), have been associated with lipid metabolism and many chronic inflammatory disorders. In this study, we asked if these neuropeptides are associated with LPP and FFA scalp lesions. Alteration in the expression of SP and CGRP in affected and unaffected scalp skin from patients with both diseases was found with examination of sections using immunohistochemical techniques and confocal microscopy. We then quantitatively assessed and compared SP and CGRP expression from control, LPP and FFA scalp biopsies. Although LPP and FFA share similar histopathologic findings, opposite results were found in affected and unaffected scalp in the ELISA tests, suggesting that these diseases may have different pathogenic mechanisms. We also found presence of histopathological inflammation irrespective of evident clinical lesions, which raises the possibility that both diseases may be more generalized processes affecting the scalp.

Identifiants

pubmed: 30408256
doi: 10.1111/exd.13835
doi:

Substances chimiques

Neuropeptides 0
Substance P 33507-63-0
Calcitonin Gene-Related Peptide JHB2QIZ69Z

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

282-285

Subventions

Organisme : Goltz Professorship, University of Minnesota Department of Dermatology
Pays : International

Informations de copyright

© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Références

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C. Chiang, D. Sah, B. K. Cho, B. E. Ochoa, V. H. Price, J. Am. Acad. Dermatol. 2010, 62, 387.
E. M. Peters, M. E. Ericson, J. Hosoi, K. Seiffert, M. K. Hordinsky, J. C. Ansel, R. Paus, T. E. Scholzen, J. Invest. Dermatol. 1937, 2006, 126.
C. S. Walker, D. L. Hay, S. M. Fitzpatrick, G. J. Cooper, K. M. Loomes, Peptides 2014, 58, 14.
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Auteurs

Isabella Doche (I)

Department of Dermatology, University of São Paulo, São Paulo, Brazil.

George L Wilcox (GL)

Departments of Dermatology, Pharmacology and Neuroscience, University of Minnesota, Minneapolis, Minnesota.

Marna Ericson (M)

Department of Dermatology, University of Minnesota, Minneapolis, Minnesota.

Neusa S Valente (NS)

Department of Dermatology, University of São Paulo, São Paulo, Brazil.

Ricardo Romiti (R)

Department of Dermatology, University of São Paulo, São Paulo, Brazil.

Brian D McAdams (BD)

Department of Neurology, University of Minnesota, Minneapolis, Minnesota.

Maria K Hordinsky (MK)

Department of Dermatology, University of Minnesota, Minneapolis, Minnesota.

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