Metabolomics profiling predicts outcome of tocilizumab in rheumatoid arthritis: an exploratory study

Introduction To study metabolic signatures can be used to identify predictive biomarkers for a patient's therapeutic response. Objectives We hypothesized that the characterization of a patients' metabolic profile, utilizing one-dimensional nuclear magnetic resonance (H-1-NMR), may predict...

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Detalles Bibliográficos
Autores: Murillo-Saich, JD, Diaz-Torne, C, Ortiz, MA, Coras, R, Gil-Alabarse, P, Pedersen, A, Corominas, H, Vidal, S, Guma, M
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2021
País:España
Institución:Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
Repositorio:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
OAI Identifier:oai:iibsantpau.fundanetsuite.com:p4389
Acceso en línea:https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4389
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810395
Access Level:acceso abierto
Palabra clave:Metabolomic profiling
Tocilizumab
Therapeutic response
Rheumatoid arthritis
NMR
Descripción
Sumario:Introduction To study metabolic signatures can be used to identify predictive biomarkers for a patient's therapeutic response. Objectives We hypothesized that the characterization of a patients' metabolic profile, utilizing one-dimensional nuclear magnetic resonance (H-1-NMR), may predict a response to tocilizumab in patients with rheumatoid arthritis (RA). Methods 40 active RA patients meeting the 2010 ACR/EULAR classification criteria initiating treatment with tocilizumab were recruited. Clinical outcomes were determined at baseline, and after six and twelve months of treatment. EULAR response criteria at 6 and 12 months to categorize patients as responders and non-responders. Blood was collected at baseline and after six months of tocilizumab therapy. H-1-NMR was used to acquire a spectra of plasma samples. Chenomx NMR suite 8.5 was used for metabolite identification and quantification. SPSS v.27 and MetaboAnalyst 4.0 were used for statistical and pathway analysis. Results Isobutyrate, 3-hydroxybutyrate, lysine, phenylalanine, sn-glycero-3-phosphocholine, tryptophan and tyrosine were significantly elevated in responders at the baseline. OPLS-DA at baseline partially discriminated between RA responders and non-responders. A multivariate diagnostic model showed that concentrations of 3-hydroxybutyrate and phenylalanine improved the ability to specifically predict responders classifying 77.1% of the patients correctly. At 6 months, levels of methylamine, sn-glycero-3-phosphocholine and tryptophan tended to still be low in non-responders. Conclusion The relationship between plasma metabolic profiles and the clinical response to tocilizumab suggests that H-1-NMR may be a promising tool for RA therapy optimization. More studies are needed to determine if metabolic profiling can predict the response to biological therapies in RA patients.