Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect

Author:

Styrkarsdottir UnnurORCID,Stefansdottir Lilja,Thorleifsson Gudmar,Stefansson Olafur A,Saevarsdottir SaedisORCID,Lund Sigrun H,Rafnar Thorunn,Hoshijima Kazuyuki,Novak Kendra,Oreiro Natividad,Rego-Perez IgnacioORCID,Hansen Channing,Kazmers Nikolas,Kiemeney Lambertus A,Blanco Francisco JORCID,Barker Tyler,Kloppenburg MargreetORCID,Jurynec Michael JORCID,Gudbjartsson Daniel F,Jonsson Helgi,Thorsteinsdottir Unnur,Stefansson Kari

Abstract

ObjectivesErosive hand osteoarthritis (EHOA) is a severe subset of hand osteoarthritis (OA). It is unclear if EHOA is genetically different from other forms of OA. Sequence variants at ten loci have been associated with hand OA but none with EHOA.MethodsWe performed meta-analysis of EHOA in 1484 cases and 550 680 controls, from 5 populations. To identify causal genes, we performed eQTL and plasma pQTL analyses, and developed one zebrafish mutant. We analysed associations of variants with other traits and estimated shared genetics between EHOA and other traits.ResultsFour common sequence variants associated with EHOA, all with relatively high effect. Rs17013495 (SPP1/MEPE, OR=1.40, p=8.4×10−14) and rs11243284 (6p24.3, OR=1.35, p=4.2×10−11) have not been associated with OA, whereas rs11631127 (ALDH1A2, OR=1.46, p=7.1×10−18), and rs1800801 (MGP, OR=1.37, p=3.6×10−13) have previously been associated with hand OA. The association of rs1800801 (MGP) was consistent with a recessive mode of inheritance in contrast to its additive association with hand OA (OR homozygotes vs non-carriers=2.01, 95% CI 1.71 to 2.37). All four variants associated nominally with finger OA, although with substantially lower effect. We found shared genetic components between EHOA and other OA measures, grip strength, urate levels and gout, but not rheumatoid arthritis. We identifiedALDH1A2,MGPandBMP6as causal genes for EHOA, with loss-of-functionBmp6zebrafish mutants displaying EHOA-like phenotypes.ConclusionsWe report on significant genetic associations with EHOA. The results support the view of EHOA as a form of severe hand OA and partly separate it from OA in larger joints.

Funder

UK Biobank

Arthritis Society

deCODE genetics / Amgen Inc

Publisher

BMJ

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,Immunology and Allergy,Rheumatology

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