Genome‐wide association study of degenerative bony changes of the temporomandibular joint. (9th June 2013)

• Record Type: Journal Article
• Authors: Yamaguchi, T; Nakaoka, H; Yamamoto, K; Fujikawa, T; Kim, Y‐I; Yano, K; Haga, S; Katayama, K; Shibusawa, T; Park, SB; Maki, K; Kimura, R; Inoue, I
• Is Part Of: Oral diseases. Volume 20:Number 4(2014:May)
• Page Start: 409
• Page End: 415
• Publication Date: 2013-06-09
• Subjects: genome‐wide association study (GWAS) -- temporo‐mandibular joint (TMJ) -- degeneration -- osteoarthritis; Mouth -- Diseases -- Research -- Periodicals; 617.522
• DOI: 10.1111/odi.12141
• Languages: English
• ISSNs: 1354-523X

Abstract

Abstract : Objectives: To identify susceptibility genes underlying degenerative bony changes of the temporomandibular joint (TMJ). Materials and Methods: Bony changes of the TMJ condylar head were diagnosed by examination of panoramic radiographs and/or magnetic resonance images and/or computed tomography images. We conducted a genome‐wide association study (GWAS) of 146 cases with TMJ degeneration and 374 controls from East Asian populations using an Illumina HumanOmniExpress BeadChip. After rigorous quality‐control filtering, approximately 550 000 single nucleotide polymorphisms (SNPs) were used for tests of associations with disease status. Results: Forty‐one SNPs at 22 independent loci showed association signals at P < 1 × 10 −4 . The SNP rs878962, which maps on an intron of TSPAN9 on chromosome 12, showed the strongest association (combined OR = 1.89, 95% confidence interval = 1.43–2.50, P = 8.1 × 10 −6 ). According to in silico predictions of the 41 SNPs, two intronic SNPs of APOL3 (rs80575) and MRC2 (rs2460300) may fall within regulatory elements and affect DNA–protein interactions. We could not replicate SNPs located on genes that have been reported to be associated with temporomandibular disorder or temporomandibular osteoarthritis in previous studies at P < 1 × 10 −4 . Conclusions: Our GWAS identified 22 independent loci showing suggestive association signals with degenerative bony changes of the TMJ. These loci provide good candidates for future follow‐up studies.