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Meta-analysis of filaggrin polymorphisms in eczema and asthma: Robust risk factors in atopic disease

Lookup NU author(s): Dr Sara Brown, Professor Heather Cordell

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Abstract

Background: The discovery of filaggrin (FLG) null mutations as a major risk factor for eczema represents a milestone toward the understanding of an important mechanism in this complex disease. However, published studies demonstrate differences concerning design and effect size, and conflicting results for asthma have been reported. Objectives: We sought to provide a more accurate estimate of FLG effect sizes and to better refine FLG risk profiles within the broad and inclusive eczema diagnosis. We also sought to provide a more detailed and conclusive estimate of the risk for asthma associated with FLG null alleles. Methods: We performed a meta-analysis of 24 studies on FLG mutations and eczema involving 5,791 cases, 26,454 control subjects, and 1,951 families as well as 17 studies on asthma involving 3,138 cases, 17,164 control subjects, and 1,511 offspring. Results: Both case-control and family studies showed strong associations with eczema. Case-control studies were heterogeneous, whereas family studies yielded more homogeneous results. Combined analysis showed that FLG haploinsufficiency strongly increases the eczema risk (odds ratio [OR], 3.12; 95% CI, 2.57-3.79) and is associated with more severe and dermatologist-diagnosed disease. FLG mutations are also significantly associated with asthma (OR, 1.48; 95% CI, 1.32-1.66). However, although strong effects for the compound phenotype asthma plus eczema (OR, 3.29; 95% CI, 2.84-3.82) were observed, there appears to be no association with asthma in the absence of eczema. Conclusions: This meta-analysis summarizes the strong evidence for a high eczema risk conferred by FLG mutations and refines their risk profiles, suggesting an association with more severe and secondary care disease. FLG mutations are also a robust risk factor for asthma and might help define the asthma endophenotype linked with eczema. (J Allergy Clin Immunol 2009;123:1361-70.)


Publication metadata

Author(s): Rodriguez E, Baurecht H, Herberich E, Wagenpfeil S, Brown SJ, Cordell HJ, Irvine AD, Weidinger S

Publication type: Article

Publication status: Published

Journal: Journal of Allergy and Clinical Immunology

Year: 2009

Volume: 123

Issue: 6

Pages: 1361-1370

ISSN (print): 0091-6749

ISSN (electronic): 1097-6825

Publisher: Mosby, Inc.

URL: http://dx.doi.org/10.1016/j.jaci.2009.03.036

DOI: 10.1016/j.jaci.2009.03.036


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Funding

Funder referenceFunder name
Wilhelm-Vaillant-Stiftung
01GS0818German Ministry of Education and Research (BMBF)
C49-08University Hospital Rechts der Isar, Technische Universitat Munchen
KKF-27/05University Hospital Rechts der Isar, Technische Universitat Munchen
KKF-07/04University Hospital Rechts der Isar, Technische Universitat Munchen
WE 2678/4-1DFG

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