1H NMR Metabolomics Identifies Underlying Inflammatory Pathology in Osteoarthritis and Rheumatoid Arthritis Synovial Joints

被引:80
作者
Anderson, James R. [1 ]
Chokesuwattanaskul, Susama [2 ,3 ]
Phelan, Marie M. [2 ,4 ]
Welting, Tim J. M. [5 ]
Lian, Lu-Yun [2 ]
Peffers, Mandy J. [1 ]
Wright, Helen L. [1 ]
机构
[1] Univ Liverpool, Inst Ageing & Chron Dis, Liverpool L7 8TX, Merseyside, England
[2] Univ Liverpool, Inst Integrat Biol, Liverpool L69 7ZB, Merseyside, England
[3] Chulalongkorn Univ, Bangkok 10330, Thailand
[4] Univ Liverpool, HLS Technol Directorate, Liverpool L7 8TX, Merseyside, England
[5] Maastricht Univ, Med Ctr, Dept Orthoped Surg, Lab Expt Orthoped, NL-6229 HX Maastricht, Netherlands
基金
英国惠康基金; 英国医学研究理事会;
关键词
synovial fluid; metabolomics; osteoarthritis; rheumatoid arthritis; nuclear magnetic resonance; FLUID; CARTILAGE; SERUM; MECHANISMS; CYTOKINES; DIAGNOSIS; PROFILES; PLASMA; URINE; CELLS;
D O I
10.1021/acs.jproteome.8b00455
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Despite osteoarthritis (OA) and rheumatoid arthritis (RA) being typically age-related, their underlying etiologies are markedly different. We used H-1 nuclear magnetic resonance (NMR) spectroscopy to identify differences in metabolite profiles in low volumes of OA and RA synovial fluid (SF). SF was aspirated from knee joints of 10 OA and 14 RA patients. 100 mu L SF was analyzed using a 700 MHz Avance IIIHD Bruker NMR spectrometer with a TCI cryoprobe. Spectra were analyzed by Chenomx, Bruker TopSpin and AMIX software. Statistical analysis was undertaken using Metaboanalyst. 50 metabolites were annotated, including amino acids, saccharides, nucleotides and soluble lipids. Discriminant analysis identified group separation between OA and RA cohorts, with 32 metabolites significantly different between OA and RA SF (false discovery rate (FDR) < 0.05). Metabolites of glycolysis and the tricarboxylic acid cycle were lower in RA compared to OA; these results concur with higher levels of inflammation, synovial proliferation and hypoxia found in RA compared to OA. Elevated taurine in OA may indicate increased subchondral bone sclerosis. We demonstrate that quantifiable differences in metabolite abundance can be measured in low volumes of SF by H-1 NMR spectroscopy, which may be clinically useful to aid diagnosis and improve understanding of disease pathogenesis.
引用
收藏
页码:3780 / 3790
页数:11
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