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Logo of arthrestherBioMed Centralbiomed central web sitesearchsubmit a manuscriptregisterthis articleArthritis Research & Therapy
Arthritis Res Ther. 2010; 12(3): R116.
Published online Jun 16, 2010. doi:  10.1186/ar3053
PMCID: PMC2911910
Only one independent genetic association with rheumatoid arthritis within the KIAA1109-TENR-IL2-IL21 locus in Caucasian sample sets: confirmation of association of rs6822844 with rheumatoid arthritis at a genome-wide level of significance
Jade E Hollis-Moffatt,#1 Michael Chen-Xu,#1 Ruth Topless,1 Nicola Dalbeth,2 Peter J Gow,3 Andrew A Harrison,4 John Highton,5 Peter BB Jones,2 Michael Nissen,6 Malcolm D Smith,6 Andre van Rij,7 Gregory T Jones,7 Lisa K Stamp,8 and Tony R Merrimancorresponding author1
1Department of Biochemistry, 710 Cumberland Street, University of Otago, Dunedin 9054, New Zealand
2Department of Medicine, 85 Park Road, University of Auckland, Auckland 1142, New Zealand
3Department of Rheumatology, Middlemore Hospital, Hospital Road, Auckland 1640, New Zealand
4Department of Medicine, 23A Mein Street, University of Otago, Wellington 6242, New Zealand
5Department of Medicine, Great King Street, University of Otago, Dunedin 9054, New Zealand
6Department of Medicine, Daws Road, Flinders Medical Centre and Repatriation General Hospital, Adelaide 5041, Australia
7Department of Surgery, Great King Street, University of Otago, Dunedin 9054, New Zealand
8Department of Medicine, Riccarton Avenue, University of Otago, Christchurch 8140, New Zealand
corresponding authorCorresponding author.
#Contributed equally.
Jade E Hollis-Moffatt: jade.hollis-moffatt/at/; Michael Chen-Xu: chemi166/at/; Ruth Topless: ruth.mccallum/at/; Nicola Dalbeth: n.dalbeth/at/; Peter J Gow: PGow/at/; Andrew A Harrison: andrew.harrison/at/; John Highton: john.highton/at/; Peter BB Jones: p.jones/at/; Michael Nissen: michaelnissen/at/; Malcolm D Smith: malcolm.Smith/at/; Andre van Rij: andre.vanrij/at/; Gregory T Jones: greg.jones/at/; Lisa K Stamp: lisaStamp/at/; Tony R Merriman: tony.merriman/at/
Received April 7, 2010; Revised May 25, 2010; Accepted June 16, 2010.
The single nucleotide polymorphism (SNP) rs6822844 within the KIAA1109-TENR-IL2-IL21 gene cluster has been associated with rheumatoid arthritis (RA). Other variants within this cluster, including rs17388568 that is not in linkage disequilibrium (LD) with rs6822844, and rs907715 that is in moderate LD with rs6822844 and rs17388568, have been associated with a number of autoimmune phenotypes, including type 1 diabetes (T1D). Here we aimed to: one, confirm at a genome-wide level of significance association of rs6822844 with RA and, two, evaluate whether or not there were effects independent of rs6822844 on RA at the KIAA1109-TENR-IL2-IL21 locus.
A total of 842 Australasian RA patients and 1,115 controls of European Caucasian ancestry were genotyped for rs6822844, rs17388568 and rs907715. Meta-analysis of these data with published and publicly-available data was conducted using STATA.
No statistically significant evidence for association was observed in the Australasian sample set for rs6822844 (odds ratio (OR) = 0.95 (0.80 to 1.12), P = 0.54), or rs17388568 (OR = 1.03 (0.90 to 1.19), P = 0.65) or rs907715 (OR = 0.98 (0.86 to 1.12), P = 0.69). When combined in a meta-analysis using data from a total of 9,772 cases and 10,909 controls there was a genome-wide level of significance supporting association of rs6822844 with RA (OR = 0.86 (0.82 to 0.91), P = 8.8 × 10-8, P = 2.1 × 10-8 including North American Rheumatoid Arthritis Consortium data). Meta-analysis of rs17388568, using a total of 6,585 cases and 7,528 controls, revealed no significant association with RA (OR = 1.03, (0.98 to 1.09); P = 0.22) and meta-analysis of rs907715 using a total of 2,689 cases and 4,045 controls revealed a trend towards association (OR = 0.93 (0.87 to 1.00), P = 0.07). However, this trend was not independent of the association at rs6822844.
The KIAA1109-TENR-IL2-IL21 gene cluster, that encodes an interleukin (IL-21) that plays an important role in Th17 cell biology, is the 20th locus for which there is a genome-wide (P ≤ 5 ×10-8) level of support for association with RA. As for most other autoimmune diseases, with the notable exception of T1D, rs6822844 is the dominant association in the locus. The KIAA1109-TENR-IL2-IL21 locus also confers susceptibility to other autoimmune phenotypes with a heterogeneous pattern of association.
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