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(1)H NMR Metabolomics Identifies Underlying Inflammatory Pathology in Osteoarthritis and Rheumatoid Arthritis Synovial Joints
[Image: see text] Despite osteoarthritis (OA) and rheumatoid arthritis (RA) being typically age-related, their underlying etiologies are markedly different. We used (1)H nuclear magnetic resonance (NMR) spectroscopy to identify differences in metabolite profiles in low volumes of OA and RA synovial...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220363/ https://www.ncbi.nlm.nih.gov/pubmed/30229649 http://dx.doi.org/10.1021/acs.jproteome.8b00455 |
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author | Anderson, James R. Chokesuwattanaskul, Susama Phelan, Marie M. Welting, Tim J. M. Lian, Lu-Yun Peffers, Mandy J. Wright, Helen L. |
author_facet | Anderson, James R. Chokesuwattanaskul, Susama Phelan, Marie M. Welting, Tim J. M. Lian, Lu-Yun Peffers, Mandy J. Wright, Helen L. |
author_sort | Anderson, James R. |
collection | PubMed |
description | [Image: see text] Despite osteoarthritis (OA) and rheumatoid arthritis (RA) being typically age-related, their underlying etiologies are markedly different. We used (1)H 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 μL 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 (1)H NMR spectroscopy, which may be clinically useful to aid diagnosis and improve understanding of disease pathogenesis. |
format | Online Article Text |
id | pubmed-6220363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-62203632018-11-08 (1)H NMR Metabolomics Identifies Underlying Inflammatory Pathology in Osteoarthritis and Rheumatoid Arthritis Synovial Joints Anderson, James R. Chokesuwattanaskul, Susama Phelan, Marie M. Welting, Tim J. M. Lian, Lu-Yun Peffers, Mandy J. Wright, Helen L. J Proteome Res [Image: see text] Despite osteoarthritis (OA) and rheumatoid arthritis (RA) being typically age-related, their underlying etiologies are markedly different. We used (1)H 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 μL 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 (1)H NMR spectroscopy, which may be clinically useful to aid diagnosis and improve understanding of disease pathogenesis. American Chemical Society 2018-09-19 2018-11-02 /pmc/articles/PMC6220363/ /pubmed/30229649 http://dx.doi.org/10.1021/acs.jproteome.8b00455 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Anderson, James R. Chokesuwattanaskul, Susama Phelan, Marie M. Welting, Tim J. M. Lian, Lu-Yun Peffers, Mandy J. Wright, Helen L. (1)H NMR Metabolomics Identifies Underlying Inflammatory Pathology in Osteoarthritis and Rheumatoid Arthritis Synovial Joints |
title | (1)H
NMR Metabolomics Identifies Underlying Inflammatory Pathology in Osteoarthritis
and Rheumatoid Arthritis Synovial Joints |
title_full | (1)H
NMR Metabolomics Identifies Underlying Inflammatory Pathology in Osteoarthritis
and Rheumatoid Arthritis Synovial Joints |
title_fullStr | (1)H
NMR Metabolomics Identifies Underlying Inflammatory Pathology in Osteoarthritis
and Rheumatoid Arthritis Synovial Joints |
title_full_unstemmed | (1)H
NMR Metabolomics Identifies Underlying Inflammatory Pathology in Osteoarthritis
and Rheumatoid Arthritis Synovial Joints |
title_short | (1)H
NMR Metabolomics Identifies Underlying Inflammatory Pathology in Osteoarthritis
and Rheumatoid Arthritis Synovial Joints |
title_sort | (1)h
nmr metabolomics identifies underlying inflammatory pathology in osteoarthritis
and rheumatoid arthritis synovial joints |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220363/ https://www.ncbi.nlm.nih.gov/pubmed/30229649 http://dx.doi.org/10.1021/acs.jproteome.8b00455 |
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