Polymorphism in the 5 ' regulatory region of the B-lymphocyte activating factor gene is associated with the Ro/La autoantibody response and serum BAFF levels in primary Sjogren's syndrome
dc.contributor.author | Nossent, J. | |
dc.contributor.author | Lester, S. | |
dc.contributor.author | Zahra, D. | |
dc.contributor.author | Mackay, C. | |
dc.contributor.author | Rischmueller, M. | |
dc.date.issued | 2008 | |
dc.description.abstract | Objective. To investigate the association between haplotypes in the 5' regulatory region of the B-lymphocyte activating factor (BAFF) gene, disease susceptibility and serum BAFF (s-BAFF) levels in Caucasian primary SS (pSS) patients. Methods. Case–control study in an established pSS cohort with PCR–RFLP genotyping for four SNPs (-2841 TC, -2704 TC, -2701 TA, -871 CT), which tag a haplotype block in the 5' regulatory region of the BAFF gene and s-BAFF determination by ELISA. Results. s-BAFF levels were elevated in Ro/La-positive pSS patients (n = 85, 1770 pg/ml) compared with both Ro/La-negative pSS patients (n = 27, 1193 pg/ml) and controls (n = 59, 1171 pg/ml), P < 0.001. s-BAFF increased with diversification of the anti-Ro/La antibody response, but was not correlated with age, RF or immunoglobulin G levels. There were four common BAFF haplotypes. While the CTAT haplotype was associated with Ro/La-positive pSS [odds ratio (OR) 2.6; 95% CI 1.7, 4.1; P = 0.00004], the TTTT haplotype was associated with elevated s-BAFF in autoantibody-positive pSS (n = 85; 88% females; P = 0.008). The shared -871 T allele had no independent contribution to disease susceptibility or s-BAFF. Conclusions. Disease susceptibility for Ro/La-positive pSS is increased with the CTAT haplotype, but not associated with high s-BAFF levels. Elevated s-BAFF levels in pSS are associated with the TTTT haplotype and may be a secondary phenomenon in Ro/La-positive pSS. While both haplotypes carry the -871 T allele, this allele is not independently associated with disease susceptibility. | |
dc.description.statementofresponsibility | J. C. Nossent, S. Lester, D. Zahra, C. R. Mackay and M. Rischmueller | |
dc.identifier.citation | Rheumatology, 2008; 47(9):1311-1316 | |
dc.identifier.doi | 10.1093/rheumatology/ken246 | |
dc.identifier.issn | 1462-0324 | |
dc.identifier.issn | 1462-0332 | |
dc.identifier.orcid | Lester, S. [0000-0003-3013-2701] | |
dc.identifier.orcid | Rischmueller, M. [0000-0001-5057-3286] | |
dc.identifier.uri | http://hdl.handle.net/2440/54107 | |
dc.language.iso | en | |
dc.publisher | Oxford Univ Press | |
dc.source.uri | https://doi.org/10.1093/rheumatology/ken246 | |
dc.subject | B-lymphocyte activating factor | |
dc.subject | Sjögren's syndrome | |
dc.subject | Polymorphism | |
dc.title | Polymorphism in the 5 ' regulatory region of the B-lymphocyte activating factor gene is associated with the Ro/La autoantibody response and serum BAFF levels in primary Sjogren's syndrome | |
dc.type | Journal article | |
pubs.publication-status | Published |