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Genome-wide association and functional studies identify a role for matrix Gla protein in osteoarthritis of the hand

Title: Genome-wide association and functional studies identify a role for matrix Gla protein in osteoarthritis of the hand
Authors: Hollander, Wouter den; Boer, Cindy G.; Hart, Deborah J.; Yau, Michelle S.; Ramos, Yolande F.M.; Metrustry, Sarah; Broer, Linda; Deelen, Joris; Cupples, L. Adrienne; Rivadeneira, Fernando; Kloppenburg, Margreet; Peters, Marjolein; Spector, Tim D.; Hofman, Albert; Slagboom, P. Eline; Nelissen, Rob G.H.H.; Uitterlinden, Andr� G.; Felson, David T.; Valdes, Ana M.; Meulenbelt, Ingrid; van Meurs, Joyce J.B.
Publisher Information: BMJ Publishing Group
Publication Year: 2017
Collection: University of Nottingham: Repository@Nottingham
Description: Objective Osteoarthritis (OA) is the most common form of arthritis and the leading cause of disability in the elderly. Of all the joints, genetic predisposition is strongest for OA of the hand; however, only few genetic risk loci for hand OA have been identified. Our aim was to identify novel genes associated with hand OA and examine the underlying mechanism.Methods We performed a genome-wide association study of a quantitative measure of hand OA in 12 784 individuals (discovery: 8743, replication: 4011). Genome-wide significant signals were followed up by analysing gene and allele-specific expression in a RNA sequencing dataset (n=96) of human articular cartilage.Results We found two significantly associated loci in the discovery set: at chr12 (p=3.5 × 10⁻¹⁰) near the matrix Gla protein (MGP) gene and at chr12 (p=6.1×10⁻⁹) near the CCDC91 gene. The DNA variant near the MGP gene was validated in three additional studies, which resulted in a highly significant association between the MGP variant and hand OA (rs4764133, Betameta=0.83, Pmeta=1.8*10⁻¹⁵). This variant is high linkage disequilibrium with a coding variant in MGP, a vitamin K-dependent inhibitor of cartilage calcification. Using RNA sequencing data from human primary cartilage tissue (n=96), we observed that the MGP RNA expression of the hand OA risk allele was significantly lowercompared with the MGP RNA expression of the reference allele (40.7%, p
Document Type: article in journal/newspaper
Language: English
Relation: https://nottingham-repository.worktribe.com/output/883199; Annals of the Rheumatic Diseases
DOI: 10.1136/annrheumdis-2017-211214
Availability: https://doi.org/10.1136/annrheumdis-2017-211214; https://nottingham-repository.worktribe.com/file/883199/1/Hollander.Boer.et.al.MGP.manuscript.2017.rebuttal.Final_2_nomarkups.pdf; https://nottingham-repository.worktribe.com/output/883199
Rights: openAccess
Accession Number: edsbas.80019EC
Database: BASE