New genomic region for Wegener's granulomatosis as revealed by an extended association screen with 202 apoptosis-related genes

Peter Jagiello*, Martin Gencik, Larissa Arning, Stefan Wieczorek, Erdmute Kunstmann, Elena Csernok, Wolfgang L. Gross, Joerg T. Epplen

*Corresponding author for this work
112 Citations (Scopus)


Wegener's granulomatosis (WG) is a systemic disease with complex genetic background. It is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis and the presence of antineutrophil cytoplasmatic autoantibodies (C-ANCAs) in sera of patients. Here, we report on an extended association screen (EAS) with 202 microsatellite markers, representing apoptosis-related genes and further genes down-regulated in apoptotic neutrophils, using pooled DNA of 150 Northern German patients suffering from WG and 100 healthy Northern German controls. Six microsatellite allele patterns were found significantly associated with WG, three of which could be confirmed by individual genotyping. One marker remained significantly associated after multiple corrections. This marker representing the retinoid X receptor β gene (RXRB, P= 7.60×10-6, distance to gene: ∼ 5.3 kb) is localised in the major histocompatibility complex (MHC) region between the HLA-DPB1 and DAXX genes. HLA-DPB1 typing and fine mapping of the region with additional microsatellites and single-nucleotide polymorphisms (SNPs) revealed a strong association of WG with the significantly over-represented DPB1*0401 (P=1.51×10-10, OR=3.91) allele compared with the control cohort. In addition, an extended haplotype DPB1* 0401/RXRB03 was identified showing an even stronger association with WG (P=7.13×10-17, OR=6.41). These results represent the strongest association of a genomic region with WG, suggesting a major genetic contribution in the aetiology of the disease. Thus, our data demonstrate that EAS may be a valuable alternative approach for determining genetic predisposition factors in multifactorial diseases.

Original languageEnglish
JournalHuman Genetics
Issue number5
Pages (from-to)468-477
Number of pages10
Publication statusPublished - 04.2004

Research Areas and Centers

  • Academic Focus: Center for Infection and Inflammation Research (ZIEL)


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