Detecting novel micro RNAs in rheumatoid arthritis with gene-based association testing

Aleksander Lenert, David W. Fardo

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

Objective To identify novel risk genes by gene-based association analysis in rheumatoid arthritis (RA). Methods We performed gene-based association testing with GATES (Gene-based Association Test using Extended Simes procedure) to augment the power of genomewide-association study (GWAS) results from the largest meta-GWAS by Okada et al. in 14,361 RA cases and 43,923 controls of European ancestry using 8,694,488 SNPs. Results We identified 115 genes significantly associated with RA by gene-based association testing corresponding to 43 RA risk loci; 23 risk loci contained a single top risk gene, while 20 risk loci contained two or more risk genes. We replicated 39 of the genomewide significant risk loci identified by Okada et al. in Europeans with RA; we found identical top genes for 26 loci. Our gene-based testing identified 6 new top gene hits for each of the following 6 RA risk loci: RPP14 (for DNASE1L3-ABHD6-PXK), PXT1 (for ETV7), MIR5708 (for TPD52), DDX6 (for CXCR5), SUOX (for CDK2), and PCAT29 (for LOC145837). We also identified a potential novel RA risk locus (11q23.3, start position 118528941 bp) which contains the following 3 genes: TREH-PHLDB1-MIR6716; the locus was not identified previously but may be a proxy for CXCR5. Conclusion Through novel comprehensive gene-based association testing in > 50,000 Europeans with RA using ~8 million SNPs, we confirmed prior RA risk loci and identified novel risk genes including non-coding regulatory miRNAs, providing further insight into the complex genetics of RA.

Original languageEnglish
Pages (from-to)586-592
Number of pages7
JournalClinical and Experimental Rheumatology
Volume35
Issue number4
StatePublished - 2017

Bibliographical note

Publisher Copyright:
© Clinical and Experimental Rheumatology 2017.

Funding

We would like to thank Okada et al. for the publically available data used in our study. This work was supported in part by an NIH grant K25AG043546 (DWF).

FundersFunder number
National Institutes of Health (NIH)
National Institute on AgingK25AG043546
National Institute on Aging
Donald Woods Foundation

    Keywords

    • Gene-based association testing
    • Genomewide association testing
    • Micro RNA
    • Rheumatoid arthritis
    • Risk genes

    ASJC Scopus subject areas

    • Rheumatology
    • Immunology and Allergy
    • Immunology

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