| Literature DB >> 30374069 |
Unnur Styrkarsdottir1, Sigrun H Lund2,3, Gudmar Thorleifsson2, Florian Zink2, Olafur A Stefansson2, Jon K Sigurdsson2, Kristinn Juliusson2, Kristbjörg Bjarnadottir2, Sara Sigurbjornsdottir4, Stefan Jonsson2, Kristjan Norland2, Lilja Stefansdottir2, Asgeir Sigurdsson2, Gardar Sveinbjornsson2, Asmundur Oddsson2, Gyda Bjornsdottir2, Reynir L Gudmundsson2, Gisli H Halldorsson2, Thorunn Rafnar2, Ingileif Jonsdottir2,3,5, Eirikur Steingrimsson4, Gudmundur L Norddahl2, Gisli Masson2, Patrick Sulem2, Helgi Jonsson3,6, Thorvaldur Ingvarsson3,7,8, Daniel F Gudbjartsson2,9, Unnur Thorsteinsdottir2,3, Kari Stefansson10,11.
Abstract
Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we describe the largest meta-analysis so far of osteoarthritis of the hip and the knee in samples from Iceland and the UK Biobank (including 17,151 hip osteoarthritis patients, 23,877 knee osteoarthritis patients, and more than 562,000 controls). We found 23 independent associations at 22 loci in the additive meta-analyses, of which 16 of the loci were novel: 12 for hip and 4 for knee osteoarthritis. Two associations are between rare or low-frequency missense variants and hip osteoarthritis, affecting the genes SMO (rs143083812, frequency 0.11%, odds ratio (OR) = 2.8, P = 7.9 × 10-12, p.Arg173Cys) and IL11 (rs4252548, frequency 2.08%, OR = 1.30, P = 2.1 × 10-11, p.Arg112His). A common missense variant in the COL11A1 gene also associates with hip osteoarthritis (rs3753841, frequency 61%, P = 5.2 × 10-10, OR = 1.08, p.Pro1284Leu). In addition, using a recessive model, we confirm an association between hip osteoarthritis and a variant of CHADL1 (rs117018441, P = 1.8 × 10-25, OR = 5.9). Furthermore, we observe a complex relationship between height and risk of osteoarthritis.Entities:
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Year: 2018 PMID: 30374069 DOI: 10.1038/s41588-018-0247-0
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330