Filaggrin gene mutations in relation to contact allergy and hand eczema in adolescence.


Journal

Contact dermatitis
ISSN: 1600-0536
Titre abrégé: Contact Dermatitis
Pays: England
ID NLM: 7604950

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 28 08 2019
revised: 21 11 2019
accepted: 27 11 2019
pubmed: 30 11 2019
medline: 24 11 2020
entrez: 30 11 2019
Statut: ppublish

Résumé

Filaggrin is an important protein for structure and function of the skin barrier. Filaggrin gene (FLG) mutations are known to result in dry skin, impaired skin barrier, and increased risk for atopic dermatitis. However, it is not clear whether these mutations are associated with contact allergy or hand eczema in adolescence. The purpose of this study was to investigate whether FLG mutations are associated with contact allergy, self-reported hand eczema, or dry skin in adolescence. We used data from the 16-year follow-up in the BAMSE cohort, information obtained from a Web-based questionnaire including questions on hand eczema and dry skin, from FLG mutation analysis (R501X, R2447X, 2282del4), and patch testing (n = 1822). Logistic regression analyses showed no statistically significant associations between FLG mutations and contact allergy (any contact allergy, nickel allergy, or fragrance allergy) according to patch test, or self-reported hand eczema at 16 years, or hand eczema ever. However, FLG mutations were associated with self-reported dry skin at 16 years. FLG mutations are associated with self-reported dry skin at 16 years. However, in this study no consistent associations were found between FLG mutations and contact allergy or hand eczema at 16.

Sections du résumé

BACKGROUND BACKGROUND
Filaggrin is an important protein for structure and function of the skin barrier. Filaggrin gene (FLG) mutations are known to result in dry skin, impaired skin barrier, and increased risk for atopic dermatitis. However, it is not clear whether these mutations are associated with contact allergy or hand eczema in adolescence.
OBJECTIVES OBJECTIVE
The purpose of this study was to investigate whether FLG mutations are associated with contact allergy, self-reported hand eczema, or dry skin in adolescence.
METHODS METHODS
We used data from the 16-year follow-up in the BAMSE cohort, information obtained from a Web-based questionnaire including questions on hand eczema and dry skin, from FLG mutation analysis (R501X, R2447X, 2282del4), and patch testing (n = 1822).
RESULTS RESULTS
Logistic regression analyses showed no statistically significant associations between FLG mutations and contact allergy (any contact allergy, nickel allergy, or fragrance allergy) according to patch test, or self-reported hand eczema at 16 years, or hand eczema ever. However, FLG mutations were associated with self-reported dry skin at 16 years.
CONCLUSIONS CONCLUSIONS
FLG mutations are associated with self-reported dry skin at 16 years. However, in this study no consistent associations were found between FLG mutations and contact allergy or hand eczema at 16.

Identifiants

pubmed: 31782153
doi: 10.1111/cod.13444
doi:

Substances chimiques

FLG protein, human 0
Filaggrin Proteins 0
Perfume 0
S100 Proteins 0
Nickel 7OV03QG267

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

147-152

Subventions

Organisme : AFA Försäkring
Organisme : Astma- och Allergiförbundet
Organisme : Forskningsrådet om Hälsa, Arbetsliv och Välfärd
Organisme : Karolinska Institutet
Organisme : Seventh Framework Programme
ID : 29 Programme MeDALL grant agreement 261357
Organisme : Region Stockholms
Organisme : Vetenskapsrådet
Organisme : Welander-Finsen Foundation

Informations de copyright

© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Références

Rodriguez E, Baurecht H, Herberich E, et al. Meta-analysis of filaggrin polymorphisms in eczema and asthma: robust risk factors in atopic disease. J Allergy Clin Immunol. 2009;123(6):1361-70.e7.
Kezic S, Kemperman PM, Koster ES, et al. Loss-of-function mutations in the filaggrin gene lead to reduced level of natural moisturizing factor in the stratum corneum. J Invest Dermatol. 2008;128(8):2117-2119.
Palmer CN, Irvine AD, Terron-Kwiatkowski A, et al. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis. Nat Genet. 2006;38(4):441-446.
Grönhagen C, Lidén C, Wahlgren CF, et al. Hand eczema and atopic dermatitis in adolescents: a prospective cohort study from the BAMSE project. Br J Dermatol. 2015;173(5):1175-1182.
Grönhagen CM, Lidén C, Bergström A, Kull I, Wahlgren CF, Meding B. Prevalence and incidence of hand eczema in adolescence: report from BAMSE-a population-based birth cohort. Br J Dermatol. 2014;171(3):609-614.
Mortz CG, Lauritsen JM, Bindslev-Jensen C, Andersen KE. Contact allergy and allergic contact dermatitis in adolescents: prevalence measures and associations. The Odense Adolescence Cohort Study on Atopic Diseases and Dermatitis (TOACS). Acta Derm Venereol. 2002;82(5):352-358.
Thyssen JP, Johansen JD, Linneberg A, Menné T. The epidemiology of hand eczema in the general population-prevalence and main findings. Contact Dermatitis. 2010;62(2):75-87.
Sergeant A, Campbell LE, Hull PR, et al. Heterozygous null alleles in filaggrin contribute to clinical dry skin in young adults and the elderly. J Invest Dermatol. 2009;129(4):1042-1045.
Bager P, Wohlfahrt J, Thyssen JP, Melbye M. Filaggrin genotype and skin diseases independent of atopic dermatitis in childhood. Pediatr Allergy Immunol. 2016;27(2):162-168.
Flohr C, England K, Radulovic S, et al. Filaggrin loss-of-function mutations are associated with early-onset eczema, eczema severity and transepidermal water loss at 3 months of age. Br J Dermatol. 2010;163(6):1333-1336.
Böhme M, Söderhäll C, Kull I, Bergström A, van Hage M, Wahlgren CF. Filaggrin mutations increase the risk for persistent dry skin and eczema independent of sensitization. J Allergy Clin Immunol. 2012;129(4):1153-1155.
Thyssen JP, Johansen JD, Zachariae C, Menné T, Linneberg A. Xerosis is associated with atopic dermatitis, hand eczema and contact sensitization independent of filaggrin gene mutations. Acta Derm Venereol. 2013;93(4):406-410.
Wickman M, Kull I, Pershagen G, Nordvall SL. The BAMSE project: presentation of a prospective longitudinal birth cohort study. Pediatr Allergy Immunol. 2002;13(suppl 15):11-13.
Lagrelius M, Wahlgren CF, Matura M, Kull I, Lidén C. High prevalence of contact allergy in adolescence: results from the population-based BAMSE birth cohort. Contact Dermatitis. 2016;74(1):44-51.
Ekelund E, Saaf A, Tengvall-Linder M, et al. Elevated expression and genetic association links the SOCS3 gene to atopic dermatitis. Am J Hum Genet. 2006;78(6):1060-1065.
Meding B, Swanbeck G. Predictive factors for hand eczema. Contact Dermatitis. 1990;23(3):154-161.
Mortz CG, Bindslev-Jensen C, Andersen KE. Hand eczema in the Odense adolescence cohort study on atopic diseases and dermatitis (TOACS): prevalence, incidence and risk factors from adolescence to adulthood. Br J Dermatol. 2014;171(2):313-323.
Uter W, Bauer A, Bensefa-Colas L, et al. Extended documentation for hand dermatitis patients: pilot study on irritant exposures. Contact Dermatitis. 2018;79(3):168-174.
Thyssen JP, Linneberg A, Menné T, Johansen JD. The epidemiology of contact allergy in the general population-prevalence and main findings. Contact Dermatitis. 2007;57(5):287-299.
Lagrelius M, Wahlgren CF, Matura M, Bergström A, Kull I, Lidén C. A population-based study of self-reported skin exposures and symptoms in relation to contact allergy in adolescents. Contact Dermatitis. 2017;77(4):242-249.
Kluger N, Misery L, Seite S, Taieb C. Body piercing: a National Survey in France. Dermatology. 2019;235(1):71-78.
Meding B, Grönhagen CM, Bergström A, Kull I, Wrangsjö K, Lidén C. Water exposure on the hands in adolescents: a report from the BAMSE cohort. Acta Derm Venereol. 2017;97(2):188-192.
Zirwas MJ, Stechschulte SA. Moisturizer allergy: diagnosis and management. J Clin Aesthet Dermatol. 2008;1(4):38-44.
Crépy MN. Rubber: new allergens and preventive measures. Eur J Dermatol. 2016;26(6):523-530.
Shaughnessy CN, Malajian D, Belsito DV. Cutaneous delayed-type hypersensitivity in patients with atopic dermatitis: reactivity to topical preservatives. J Am Acad Dermatol. 2014;70(1):102-107.
Kohli N, Nedorost S. Inflamed skin predisposes to sensitization to less potent allergens. J Am Acad Dermatol. 2016;75(2):312-317.e1.
Julander A, Boman A, Johansson G, Lidén C. Occupational skin exposue to chemicals. Arbete och Hälsa. 2018;52(3):1-66.
Akiyama M. FLG mutations in ichthyosis vulgaris and atopic eczema: spectrum of mutations and population genetics. Br J Dermatol. 2010;162(3):472-477.
Novak N, Baurecht H, Schäfer T, et al. Loss-of-function mutations in the filaggrin gene and allergic contact sensitization to nickel. J Invest Dermatol. 2008;128(6):1430-1435.
Thyssen JP, Johansen JD, Linneberg A, et al. The association between null mutations in the filaggrin gene and contact sensitization to nickel and other chemicals in the general population. Br J Dermatol. 2010;162(6):1278-1285.
Thyssen JP, Linneberg A, Ross-Hansen K, et al. Filaggrin mutations are strongly associated with contact sensitization in individuals with dermatitis. Contact Dermatitis. 2013;68(5):273-276.
Heede NG, Thyssen JP, Thuesen BH, Linneberg A, Johansen JD. Predictive factors of self-reported hand eczema in adult Danes: a population-based cohort study with 5-year follow-up. Br J Dermatol. 2016;175(2):287-295.
Mortz CG, Andersen KE, Dellgren C, Barington T, Bindslev-Jensen C. Atopic dermatitis from adolescence to adulthood in the TOACS cohort: prevalence, persistence and comorbidities. Allergy. 2015;70(7):836-845.
Lagrelius M, Wahlgren CF, Matura M, Bergström A, Kull I, Lidén C. Atopic dermatitis at preschool age and contact allergy in adolescence: a population-based cohort study. Br J Dermatol. 2019;180(4):782-789.
Thyssen JP, Mcfadden JP, Kimber I. The multiple factors affecting the association between atopic dermatitis and contact sensitization. Allergy. 2014;69(1):28-36.

Auteurs

Maria Lagrelius (M)

Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Region Stockholm, Centre for Occupational and Environmental Medicine, Stockholm, Sweden.

Carl-Fredrik Wahlgren (CF)

Dermatology Unit, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Stockholm, Sweden.

Maria Bradley (M)

Dermatology Unit, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Stockholm, Sweden.

Erik Melén (E)

Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Science and Education, Stockholm South General Hospital, Karolinska Institutet, Stockholm, Sweden.
Sachs' Children's Hospital, Stockholm, Sweden.

Inger Kull (I)

Department of Clinical Science and Education, Stockholm South General Hospital, Karolinska Institutet, Stockholm, Sweden.
Sachs' Children's Hospital, Stockholm, Sweden.

Anna Bergström (A)

Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Region Stockholm, Centre for Occupational and Environmental Medicine, Stockholm, Sweden.

Carola Lidén (C)

Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.

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