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PMID: 16188043 Published · epublish English Journal Article Research Support, Non-U.S. Gov't

Evaluation of the toll-like receptor 6 Ser249Pro polymorphism in patients with asthma, atopic dermatitis and chronic obstructive pulmonary disease.

BMC medical genetics ·Vol. 6 ·2005-09-28 ·Pages 34

Hoffjan S, Stemmler S, Parwez Q, Petrasch-Parwez E, Arinir U, Rohde G, Reinitz-Rademacher K, Schultze-Werninghaus G, Bufe A, Epplen JT

Abstract

For allergic disorders, the increasing prevalence over the past decade has been attributed in part to the lack of microbial burden in developed countries ('hygiene hypothesis'). Variation in genes encoding toll-like receptors (TLRs) as the receptor system for the first innate immune response to microbial stimuli has been implicated in various inflammatory diseases. We evaluated here the role of a coding variation, Ser249Pro, in the TLR6 gene in the pathogenesis of asthma, atopic dermatitis (AD) and chronic obstructive pulmonary disease (COPD). Genotyping of the Ser249Pro polymorphism in 68 unrelated adult patients and 132 unrelated children with asthma, 185 unrelated patients with COPD, 295 unrelated individuals with AD and 212 healthy control subjects was performed by restriction enzyme digestion. We found a weak association of the 249Ser allele with childhood asthma (p = 0.03). Yet, significance was lost after Bonferroni correction. No association was evident for AD or COPD. Variation in TLR6 might play a role in the pathogenesis of childhood asthma.

MeSH Terms
Adolescent Adult Aged Amino Acid Substitution Asthma/diagnosis,genetics Case-Control Studies Dermatitis, Atopic/diagnosis,genetics Female Gene Frequency Genetic Predisposition to Disease Humans Male Membrane Glycoproteins/genetics Middle Aged Polymorphism, Genetic Pulmonary Disease, Chronic Obstructive/diagnosis,genetics Receptors, Cell Surface/genetics Toll-Like Receptor 6
Chemicals
Membrane Glycoproteins Receptors, Cell Surface TLR6 protein, human Toll-Like Receptor 6
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Hoffjan Sabine
Department of Human Genetics, Ruhr-University Bochum, Germany. [email protected]
Stemmler Susanne
Parwez Qumar
Petrasch-Parwez Elisabeth
Arinir Umut
Rohde Gernot
Reinitz-Rademacher Karin
Schultze-Werninghaus Gerhard
Bufe Albrecht
Epplen Jörg T
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Article Info
Journal
BMC medical genetics
Abbr.
BMC Med Genet
ISSN
1471-2350
Published
2005-09-28
Epub
2005-00-28
Pages
34
Language
English
Region
England
NLM ID
100968552
PMCID
PMC1262722
Subset
IM
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