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Identification of DIO2 as new susceptibility locus for symptomatic Osteoarthritis

Lookup NU author(s): Steffan Bos, Dr Mitsushiro Nakatomi, Professor John Loughlin

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Abstract

Osteoarthritis [MIM 165720] is a common late-onset articular joint disease for which no pharmaceutical intervention is available that attenuates the cartilage degeneration. To identify a new osteoarthritis susceptibility locus, a genome-wide linkage scan and combined linkage association analysis was applied to 179 affected siblings and 4 trios with generalized osteoarthritis (The GARP study). We tested for confirmation by association in a UK population consisting of 1478 subjects who required joint replacement and 734 controls. Additional replication was tested in 1582 population based females from the Rotterdam study that contained 94 cases with defined hip osteoarthritis and in 267 Japanese females with symptomatic hip osteoarthritis and 465 controls. Suggested evidence for linkage in the GARP study was observed on chromosome 14q32.11 (LOD=3.03, P=1.9x10(-4)). Genotyping tagging SNPs covering three important candidate genes revealed a common coding variant (rs225014; Thr92Ala) in the iodothyronine-deiodinase enzyme type 2 (D2) gene (DIO2 [MIM 601413]) which significantly explained the linkage signal (P=0.006). Confirmation and replication by association in the additional osteoarthritis studies indicated a common DIO2 haplotype, exclusively containing the minor allele of rs225014 and common allele of rs12885300, with a combined recessive odds ratio of 1.79, 95% confidence interval [CI] 1.37-2.34 with P=2.02x10(-5) in females cases with advanced / symptomatic hip osteoarthritis. The gene product of this DIO2 converts intracellular pro-hormone-3,3',5,5'-tetraiodothyronine (T4) into the active thyroid hormone 3,3',5-triiodothyronine (T3) thereby regulating intracellular levels of active T3 in target tissues such as the growth plate. Our results indicate a new susceptibility gene (DIO2) conferring risk to osteoarthritis.


Publication metadata

Author(s): Meulenbelt I, Min JL, Bos S, Riyazi N, Houwing-Duistermaat JJ, van der Wijk HJ, Kroon HM, Nakajima M, Ikegawa S, Uitterlinden AG, van Meurs JB, van der Deure WM , Visser TJ, Seymour AB, Lakenberg N, van der Breggen R , Kremer D, van Duijn CM, Kloppenburg M, Loughlin J, Slagboom PE

Publication type: Article

Publication status: Published

Journal: Human Molecular Genetics

Year: 2008

Volume: 17

Issue: 12

Pages: 1867-1875

ISSN (print): 0964-6906

ISSN (electronic): 1460-2083

Publisher: Oxford University Press

URL: http://dx.doi.org/10.1093/hmg/ddn082

DOI: 10.1093/hmg/ddn082


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