Acetate correlates with disability and immune response in multiple sclerosis
Silvia Pérez-Pérez,
María Inmaculada Domínguez-Mozo,
Aitana Alonso-Gómez,
Silvia Medina,
Noelia Villarrubia,
Jose Ignacio Fernández-Velasco,
María Ángel García-Martínez,
Estefanía García-Calvo,
Héctor Estévez,
Lucienne Costa-Frossard,
Jose C. Alvarez-Cermeño,
Jose L. Luque-Garcia,
Rafael Arroyo,
Luisa M. Villar,
Roberto Alvarez-Lafuente
Affiliations
Silvia Pérez-Pérez
Grupo de Investigación de Factores Ambientales en Enfermedades Degenerativas, Instituto de Investigación Sanitaria Hospital Clínico San Carlos (IdISSC) / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
María Inmaculada Domínguez-Mozo
Grupo de Investigación de Factores Ambientales en Enfermedades Degenerativas, Instituto de Investigación Sanitaria Hospital Clínico San Carlos (IdISSC) / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
Aitana Alonso-Gómez
Grupo de Investigación de Factores Ambientales en Enfermedades Degenerativas, Instituto de Investigación Sanitaria Hospital Clínico San Carlos (IdISSC) / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
Silvia Medina
Servicio de Inmunología, Hospital Universitario Ramón y Cajal. Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS) / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
Noelia Villarrubia
Servicio de Inmunología, Hospital Universitario Ramón y Cajal. Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS) / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
Jose Ignacio Fernández-Velasco
Servicio de Inmunología, Hospital Universitario Ramón y Cajal. Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS) / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
María Ángel García-Martínez
Grupo de Investigación de Factores Ambientales en Enfermedades Degenerativas, Instituto de Investigación Sanitaria Hospital Clínico San Carlos (IdISSC) / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
Estefanía García-Calvo
Department of Analytical Chemistry, Faculty of Chemical Sciences, Universidad Complutense de Madrid, Madrid, Spain
Héctor Estévez
Department of Analytical Chemistry, Faculty of Chemical Sciences, Universidad Complutense de Madrid, Madrid, Spain
Lucienne Costa-Frossard
Servicio de Neurología, Hospital Universitario Ramón y Cajal / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
Jose C. Alvarez-Cermeño
Servicio de Neurología, Hospital Universitario Ramón y Cajal / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
Jose L. Luque-Garcia
Department of Analytical Chemistry, Faculty of Chemical Sciences, Universidad Complutense de Madrid, Madrid, Spain
Rafael Arroyo
Department of Neurology, Hospital Universitario Quironsalud Madrid / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
Luisa M. Villar
Servicio de Inmunología, Hospital Universitario Ramón y Cajal. Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS) / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
Roberto Alvarez-Lafuente
Grupo de Investigación de Factores Ambientales en Enfermedades Degenerativas, Instituto de Investigación Sanitaria Hospital Clínico San Carlos (IdISSC) / Red Española de Esclerosis Múltiple (REEM), Madrid, Spain
Background Gut microbiota has been related to multiple sclerosis (MS) etiopathogenesis. Short-chain fatty acids (SCFA) are compounds derived from microbial metabolism that have a role in gut-brain axis. Objectives To analyse SCFA levels in plasma of MS patients and healthy donors (HD), and the possible link between these levels and both clinical data and immune cell populations. Methods Ninety-five MS patients and 54 HD were recruited. Patients were selected according to their score in the Expanded Disability Status Scale (EDSS) (49 EDSS ≤ 1.5, 46 EDSS ≥ 5.0). SCFA were studied in plasma samples by liquid chromatography-mass spectrometry. Peripheral blood mononuclear cells were studied by flow cytometry. Gender, age, treatments, EDSS and Multiple Sclerosis Severity Score (MSSS) were evaluated at the recruitment. Results Plasma acetate levels were higher in patients than in HD (p = 0.003). Patients with EDSS ≥ 5.0 had higher acetate levels than those with EDSS≤ 1.5 (p = 0.029), and HD (p = 2.97e–4). Acetate levels correlated with EDSS (r = 0.387; p = 1.08e–4) and MSSS (r = 0.265; p = 0.011). In untreated MS patients, acetate levels correlated inversely with CD4+ naïve T cells (r = − 0.550, p = 0.001) and directly with CD8+ IL-17+ cells (r = 0.557; p = 0.001). Conclusions Plasma acetate levels are higher in MS patients than in HD. In MS there exists a correlation between plasma acetate levels, EDSS and increased IL-17+ T cells. Future studies will elucidate the role of SCFA in the disease.