This application addresses broad Challenge Area (08): Genomics and specific Challenge Topic, 08-AR-101 Genotyping of Existing Cohorts in Rheumatic, Skin, and Musculoskeletal Diseases. Juvenile idiopathic arthritis (JIA) is the most common autoimmune rheumatic disease of childhood and represents a series of childhood arthropathies that are largely based on clinically defined phenotypes. The two most common subtypes, and the focus of this study, are the oligoarticular and IgM rheumatoid factor negative (RF-) polyarticular forms of JIA. It is hypothesized that there are multiple genetic variants that predispose an individual to JIA and that the subtypes of JIA will differ in at least some of their susceptibility traits. Markers for these traits can be identified by systematically applying high throughput genotyping and copy number technology in a case:control genome-wide association study (GWAS) design. Phase I (GWAS I) genotyping has been completed and includes 1.8 million single nucleotide polymorphisms (SNPs) or copy number markers for 946 JIA cases and 1000 controls (Affymetrix(R) Genome-Wide Human SNP Array 6.0). Through this challenge grant opportunity, a second GWAS (GWAS-II) is proposed for 1100 additional existing JIA samples available from U.S. investigators of the Consortium on Juvenile Arthritis Genetics (CJAG) and international collaborators in Germany. Phenotypic information includes ILAR classification, age at disease onset, and joint counts. Approximately 1450 out-of-study controls are available through the GAIN study will be used for comparison in association testing for GWAS-II. This additional dataset when combined with existing complementary data from GWAS-I provides an unprecedented opportunity to reveal novel risk factors for JIA and is necessary for advancement of the field. This information may eventually lead to treatments for these disabling diseases and in the long-term contribute to preventing disability. In additional, this opportunity will contribute to a fundamental shift toward molecular definitions and reevaluation of the present criteria for defining subtypes of disease. This research proposal tests the view that juvenile idiopathic arthritis or JIA, is influenced by many genes conferring susceptibility to and protection from disease. As the genetic basis of the major autoimmune rheumatic disease of childhood becomes evident, eventually the treatment of these disabling diseases will become possible with the long term aim of preventing disability.

Public Health Relevance

This research proposal tests the view that juvenile idiopathic arthritis or JIA, is influenced by many genes conferring susceptibility to and protection from disease. As the genetic basis of the major autoimmune rheumatic disease of childhood becomes evident, eventually the treatment of these disabling diseases will become possible with the long term aim of preventing disability.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
NIH Challenge Grants and Partnerships Program (RC1)
Project #
5RC1AR058587-02
Application #
7941791
Study Section
Special Emphasis Panel (ZRG1-PSE-J (58))
Program Officer
Wang, Yan Z
Project Start
2009-09-28
Project End
2013-06-30
Budget Start
2010-09-01
Budget End
2013-06-30
Support Year
2
Fiscal Year
2010
Total Cost
$500,000
Indirect Cost
Name
Cincinnati Children's Hospital Medical Center
Department
Type
DUNS #
071284913
City
Cincinnati
State
OH
Country
United States
Zip Code
45229
Hinks, Anne; Marion, Miranda C; Cobb, Joanna et al. (2018) Brief Report: The Genetic Profile of Rheumatoid Factor-Positive Polyarticular Juvenile Idiopathic Arthritis Resembles That of Adult Rheumatoid Arthritis. Arthritis Rheumatol 70:957-962
McIntosh, Laura A; Marion, Miranda C; Sudman, Marc et al. (2017) Genome-Wide Association Meta-Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci. Arthritis Rheumatol 69:2222-2232
Hinks, A; Bowes, J; Cobb, J et al. (2017) Fine-mapping the MHC locus in juvenile idiopathic arthritis (JIA) reveals genetic heterogeneity corresponding to distinct adult inflammatory arthritic diseases. Ann Rheum Dis 76:765-772
Liu, Ke; Kurien, Biji T; Zimmerman, Sarah L et al. (2016) X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome. Arthritis Rheumatol 68:1290-1300
Li, Yun R; Li, Jin; Zhao, Sihai D et al. (2015) Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. Nat Med 21:1018-27
Interleukin 1 Genetics Consortium (2015) Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis. Lancet Diabetes Endocrinol 3:243-53
Ombrello, Michael J; Remmers, Elaine F; Tachmazidou, Ioanna et al. (2015) HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis. Proc Natl Acad Sci U S A 112:15970-5
Cutler, David J; Zwick, Michael E; Okou, David T et al. (2015) Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping. PLoS One 10:e0128074
Hinks, Anne; Cobb, Joanna; Marion, Miranda C et al. (2013) Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. Nat Genet 45:664-9
Faraco, Juliette; Lin, Ling; Kornum, Birgitte Rahbek et al. (2013) ImmunoChip study implicates antigen presentation to T cells in narcolepsy. PLoS Genet 9:e1003270

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