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Diagnostic properties of metabolic perturbations in rheumatoid arthritis

INTRODUCTION: The aim of this study was to assess the feasibility of diagnosing early rheumatoid arthritis (RA) by measuring selected metabolic biomarkers. METHODS: We compared the metabolic profile of patients with RA with that of healthy controls and patients with psoriatic arthritis (PsoA). The m...

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Autores principales: Madsen, Rasmus K, Lundstedt, Torbjörn, Gabrielsson, Jon, Sennbro, Carl-Johan, Alenius, Gerd-Marie, Moritz, Thomas, Rantapää-Dahlqvist, Solbritt, Trygg, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241363/
https://www.ncbi.nlm.nih.gov/pubmed/21303541
http://dx.doi.org/10.1186/ar3243
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author Madsen, Rasmus K
Lundstedt, Torbjörn
Gabrielsson, Jon
Sennbro, Carl-Johan
Alenius, Gerd-Marie
Moritz, Thomas
Rantapää-Dahlqvist, Solbritt
Trygg, Johan
author_facet Madsen, Rasmus K
Lundstedt, Torbjörn
Gabrielsson, Jon
Sennbro, Carl-Johan
Alenius, Gerd-Marie
Moritz, Thomas
Rantapää-Dahlqvist, Solbritt
Trygg, Johan
author_sort Madsen, Rasmus K
collection PubMed
description INTRODUCTION: The aim of this study was to assess the feasibility of diagnosing early rheumatoid arthritis (RA) by measuring selected metabolic biomarkers. METHODS: We compared the metabolic profile of patients with RA with that of healthy controls and patients with psoriatic arthritis (PsoA). The metabolites were measured using two different chromatography-mass spectrometry platforms, thereby giving a broad overview of serum metabolites. The metabolic profiles of patient and control groups were compared using multivariate statistical analysis. The findings were validated in a follow-up study of RA patients and healthy volunteers. RESULTS: RA patients were diagnosed with a sensitivity of 93% and a specificity of 70% in a validation study using detection of 52 metabolites. Patients with RA or PsoA could be distinguished with a sensitivity of 90% and a specificity of 94%. Glyceric acid, D-ribofuranose and hypoxanthine were increased in RA patients, whereas histidine, threonic acid, methionine, cholesterol, asparagine and threonine were all decreased compared with healthy controls. CONCLUSIONS: Metabolite profiling (metabolomics) is a potentially useful technique for diagnosing RA. The predictive value was without regard to the presence of antibodies against cyclic citrullinated peptides.
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spelling pubmed-32413632011-12-17 Diagnostic properties of metabolic perturbations in rheumatoid arthritis Madsen, Rasmus K Lundstedt, Torbjörn Gabrielsson, Jon Sennbro, Carl-Johan Alenius, Gerd-Marie Moritz, Thomas Rantapää-Dahlqvist, Solbritt Trygg, Johan Arthritis Res Ther Research Article INTRODUCTION: The aim of this study was to assess the feasibility of diagnosing early rheumatoid arthritis (RA) by measuring selected metabolic biomarkers. METHODS: We compared the metabolic profile of patients with RA with that of healthy controls and patients with psoriatic arthritis (PsoA). The metabolites were measured using two different chromatography-mass spectrometry platforms, thereby giving a broad overview of serum metabolites. The metabolic profiles of patient and control groups were compared using multivariate statistical analysis. The findings were validated in a follow-up study of RA patients and healthy volunteers. RESULTS: RA patients were diagnosed with a sensitivity of 93% and a specificity of 70% in a validation study using detection of 52 metabolites. Patients with RA or PsoA could be distinguished with a sensitivity of 90% and a specificity of 94%. Glyceric acid, D-ribofuranose and hypoxanthine were increased in RA patients, whereas histidine, threonic acid, methionine, cholesterol, asparagine and threonine were all decreased compared with healthy controls. CONCLUSIONS: Metabolite profiling (metabolomics) is a potentially useful technique for diagnosing RA. The predictive value was without regard to the presence of antibodies against cyclic citrullinated peptides. BioMed Central 2011 2011-02-08 /pmc/articles/PMC3241363/ /pubmed/21303541 http://dx.doi.org/10.1186/ar3243 Text en Copyright ©2011 Madsen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Madsen, Rasmus K
Lundstedt, Torbjörn
Gabrielsson, Jon
Sennbro, Carl-Johan
Alenius, Gerd-Marie
Moritz, Thomas
Rantapää-Dahlqvist, Solbritt
Trygg, Johan
Diagnostic properties of metabolic perturbations in rheumatoid arthritis
title Diagnostic properties of metabolic perturbations in rheumatoid arthritis
title_full Diagnostic properties of metabolic perturbations in rheumatoid arthritis
title_fullStr Diagnostic properties of metabolic perturbations in rheumatoid arthritis
title_full_unstemmed Diagnostic properties of metabolic perturbations in rheumatoid arthritis
title_short Diagnostic properties of metabolic perturbations in rheumatoid arthritis
title_sort diagnostic properties of metabolic perturbations in rheumatoid arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241363/
https://www.ncbi.nlm.nih.gov/pubmed/21303541
http://dx.doi.org/10.1186/ar3243
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