A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus
By Vesela Gateva, J. Sandling, Geoffrey Hom, K. Taylor, Sharon A. Chung, Xin-Ting Sun, W. Ortmann, R. Kosoy, R. Ferreira, G. Nordmark and 26 more. Nature Genetics, 2009
832 citations recorded by the source corpus.
Genome-wide association studies have recently identified at least 15 susceptibility loci for systemic lupus erythematosus (SLE). To confirm additional risk loci, we selected SNPs from 2,466 regions that showed nominal evidence of association to SLE (P < 0.05) in a genome-wide study and genotyped them in an independent sample of 1,963 cases and 4,329 controls. This replication effort identified five new SLE susceptibility loci (P < 5 × 10−8): TNIP1 (odds ratio (OR) = 1.27), PRDM1 (OR = 1.20), JAZF1 (OR = 1.20), UHRF1BP1 (OR = 1.17) and IL10 (OR = 1.19). We identified 21 additional candidate loci with P≤ 1 × 10−5. A candidate screen of alleles previously associated with other autoimmune diseases suggested five loci (P < 1 × 10−3) that may contribute to SLE: IFIH1, CFB, CLEC16A, IL12B and SH2B3. These results expand the number of confirmed and candidate SLE susceptibility loci and implicate several key immunologic pathways in SLE pathogenesis.
Subfields: Immunology, Rheumatology
View Paper: https://www.semanticscholar.org/paper/4eb869da32160b40a630dcdc941cbefc57f5d4cb
Citations in the corpus
- Autoantibodies, autoimmune risk alleles and clinical associations in rheumatoid arthritis cases and non-RA controls in the electronic medical records (2013, neutral): “To determine the genetic basis of autoantibodies in RA cases, we tested RA (23), SLE (19,35), and celiac disease (24,36) genetic risk alleles for association with the disease-specific autoantibodies (ACPAs, ANAs, and AGTAs, respectively).”