The nickel dose–response relationship by filaggrin genotype (FLG)

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Standard

The nickel dose–response relationship by filaggrin genotype (FLG). / Ross-Hansen, Katrine; Johansen, Jeanne D; Vølund, Aage; Menné, Torkil; Thyssen, Jacob P.

I: Contact Dermatitis, Bind 71, Nr. 1, 07.2014, s. 49-53.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ross-Hansen, K, Johansen, JD, Vølund, A, Menné, T & Thyssen, JP 2014, 'The nickel dose–response relationship by filaggrin genotype (FLG)', Contact Dermatitis, bind 71, nr. 1, s. 49-53. https://doi.org/10.1111/cod.12228

APA

Ross-Hansen, K., Johansen, J. D., Vølund, A., Menné, T., & Thyssen, J. P. (2014). The nickel dose–response relationship by filaggrin genotype (FLG). Contact Dermatitis, 71(1), 49-53. https://doi.org/10.1111/cod.12228

Vancouver

Ross-Hansen K, Johansen JD, Vølund A, Menné T, Thyssen JP. The nickel dose–response relationship by filaggrin genotype (FLG). Contact Dermatitis. 2014 jul.;71(1):49-53. https://doi.org/10.1111/cod.12228

Author

Ross-Hansen, Katrine ; Johansen, Jeanne D ; Vølund, Aage ; Menné, Torkil ; Thyssen, Jacob P. / The nickel dose–response relationship by filaggrin genotype (FLG). I: Contact Dermatitis. 2014 ; Bind 71, Nr. 1. s. 49-53.

Bibtex

@article{58ca94da6f2d409cb4cbe903ba146df3,
title = "The nickel dose–response relationship by filaggrin genotype (FLG)",
abstract = "BACKGROUND: On skin contact, nickel accumulates in the stratum corneum, where it is probably bound to proteins and amino acids. One probable contributor is filaggrin, which binds nickel avidly. Filaggrin gene (FLG) null mutations lead to a complete lack of filaggrin production from the affected allele, and have been associated with an increased risk of nickel contact sensitization in German and Danish adults.OBJECTIVES: To investigate whether the experimental nickel elicitation threshold level differed between heterozygous FLG mutation and non-mutation carriers.METHOD: Thirteen nickel-sensitized female patients, seven heterozygous mutation carriers and six non-mutation carriers (genotyped for R501X, 2282del4, or R2447X), were patch tested and performed a repeated open application test (ROAT) with a nickel sulfate dilution series. Logistic threshold dose-response analyses were used to test for differences between the two groups.RESULTS: No difference was found in the dose-response relationship between FLG mutation and non-mutation carriers.CONCLUSIONS: On the basis of this small patient study, it appears that the elicitation threshold level for nickel is independent of FLG null mutation single-allele carrier status.",
keywords = "Adult, Aged, Dermatitis, Contact, Dose-Response Relationship, Drug, Epidermis, Female, Genotype, Humans, Intermediate Filament Proteins, Irritants, Middle Aged, Mutation, Nickel, Patch Tests, Phosphoproteins, Young Adult",
author = "Katrine Ross-Hansen and Johansen, {Jeanne D} and Aage V{\o}lund and Torkil Menn{\'e} and Thyssen, {Jacob P}",
note = "{\textcopyright} 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.",
year = "2014",
month = jul,
doi = "10.1111/cod.12228",
language = "English",
volume = "71",
pages = "49--53",
journal = "Contact Dermatitis",
issn = "0105-1873",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - The nickel dose–response relationship by filaggrin genotype (FLG)

AU - Ross-Hansen, Katrine

AU - Johansen, Jeanne D

AU - Vølund, Aage

AU - Menné, Torkil

AU - Thyssen, Jacob P

N1 - © 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

PY - 2014/7

Y1 - 2014/7

N2 - BACKGROUND: On skin contact, nickel accumulates in the stratum corneum, where it is probably bound to proteins and amino acids. One probable contributor is filaggrin, which binds nickel avidly. Filaggrin gene (FLG) null mutations lead to a complete lack of filaggrin production from the affected allele, and have been associated with an increased risk of nickel contact sensitization in German and Danish adults.OBJECTIVES: To investigate whether the experimental nickel elicitation threshold level differed between heterozygous FLG mutation and non-mutation carriers.METHOD: Thirteen nickel-sensitized female patients, seven heterozygous mutation carriers and six non-mutation carriers (genotyped for R501X, 2282del4, or R2447X), were patch tested and performed a repeated open application test (ROAT) with a nickel sulfate dilution series. Logistic threshold dose-response analyses were used to test for differences between the two groups.RESULTS: No difference was found in the dose-response relationship between FLG mutation and non-mutation carriers.CONCLUSIONS: On the basis of this small patient study, it appears that the elicitation threshold level for nickel is independent of FLG null mutation single-allele carrier status.

AB - BACKGROUND: On skin contact, nickel accumulates in the stratum corneum, where it is probably bound to proteins and amino acids. One probable contributor is filaggrin, which binds nickel avidly. Filaggrin gene (FLG) null mutations lead to a complete lack of filaggrin production from the affected allele, and have been associated with an increased risk of nickel contact sensitization in German and Danish adults.OBJECTIVES: To investigate whether the experimental nickel elicitation threshold level differed between heterozygous FLG mutation and non-mutation carriers.METHOD: Thirteen nickel-sensitized female patients, seven heterozygous mutation carriers and six non-mutation carriers (genotyped for R501X, 2282del4, or R2447X), were patch tested and performed a repeated open application test (ROAT) with a nickel sulfate dilution series. Logistic threshold dose-response analyses were used to test for differences between the two groups.RESULTS: No difference was found in the dose-response relationship between FLG mutation and non-mutation carriers.CONCLUSIONS: On the basis of this small patient study, it appears that the elicitation threshold level for nickel is independent of FLG null mutation single-allele carrier status.

KW - Adult

KW - Aged

KW - Dermatitis, Contact

KW - Dose-Response Relationship, Drug

KW - Epidermis

KW - Female

KW - Genotype

KW - Humans

KW - Intermediate Filament Proteins

KW - Irritants

KW - Middle Aged

KW - Mutation

KW - Nickel

KW - Patch Tests

KW - Phosphoproteins

KW - Young Adult

U2 - 10.1111/cod.12228

DO - 10.1111/cod.12228

M3 - Journal article

C2 - 24673390

VL - 71

SP - 49

EP - 53

JO - Contact Dermatitis

JF - Contact Dermatitis

SN - 0105-1873

IS - 1

ER -

ID: 138620913