The major risk alleles of age-related macular degeneration (AMD) in CFH do not play a major role in rheumatoid arthritis (RA)

L. A. Trouw, S. Böhringer, N. A. Daha, E. A. Stahl, S. Raychaudhuri, F. A. Kurreeman, G. Stoeken-Rijsbergen, J. J. Houwing-Duistermaat, T. W. Huizinga, R. E. Toes

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Because activation of the alternative pathway (AP) of the complement system is an important aspect of both age-related macular degeneration (AMD) and rheumatoid arthritis (RA), we wished to address the question whether genetic risk factors of the AP inhibitor complement factor H (CFH) for AMD would also be risk factors for RA. For this purpose we genotyped single nucleotide polymorphisms (SNPs) in a Dutch set of RA patients and controls. Similarly, a meta-analysis using a Spanish cohort of RA as well as six large genome-wide association studies (GWAS) studies was performed. For these SNPs we analysed more than 6000 patients and 20000 controls. The CFH variants, I62V, Y402H, IVS1 and IVS10, known to associate strongly with AMD, did not show a significant association with the risk of developing RA despite a strong statistical power to detect such differences. In conclusion, the major risk alleles of AMD in CFH do not have a similar effect on developing RA. © 2011 The Authors. Clinical and Experimental Immunology © 2011 British Society for Immunology.
    Original languageEnglish
    Pages (from-to)333-337
    Number of pages4
    JournalClinical and experimental immunology
    Volume166
    Issue number3
    DOIs
    Publication statusPublished - Dec 2011

    Keywords

    • Autoimmunity
    • Complement
    • Factor h
    • Genetics
    • Rheumatoid arthritis

    Fingerprint

    Dive into the research topics of 'The major risk alleles of age-related macular degeneration (AMD) in CFH do not play a major role in rheumatoid arthritis (RA)'. Together they form a unique fingerprint.

    Cite this