Gut Microbiota as a Potential Predictive Biomarker in Relapsing-Remitting Multiple Sclerosis

The influence of the microbiome on neurological diseases has been studied for years. Recent findings have shown a different composition of gut microbiota detected in patients with multiple sclerosis (MS). The role of this dysbiosis is still unknown. We analyzed the gut microbiota of 15 patients with...

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Veröffentlicht in:Genes 2022-05, Vol.13 (5), p.930
Hauptverfasser: Navarro-López, Vicente, Méndez-Miralles, María Ángeles, Vela-Yebra, Rosa, Fríes-Ramos, Ana, Sánchez-Pellicer, Pedro, Ruzafa-Costas, Beatriz, Núñez-Delegido, Eva, Gómez-Gómez, Humberto, Chumillas-Lidón, Sara, Picó-Monllor, Jose A, Navarro-Moratalla, Laura
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container_title Genes
container_volume 13
creator Navarro-López, Vicente
Méndez-Miralles, María Ángeles
Vela-Yebra, Rosa
Fríes-Ramos, Ana
Sánchez-Pellicer, Pedro
Ruzafa-Costas, Beatriz
Núñez-Delegido, Eva
Gómez-Gómez, Humberto
Chumillas-Lidón, Sara
Picó-Monllor, Jose A
Navarro-Moratalla, Laura
description The influence of the microbiome on neurological diseases has been studied for years. Recent findings have shown a different composition of gut microbiota detected in patients with multiple sclerosis (MS). The role of this dysbiosis is still unknown. We analyzed the gut microbiota of 15 patients with active relapsing-remitting multiple sclerosis (RRMS), comparing with diet-matched healthy controls. To determine the composition of the gut microbiota, we performed high-throughput sequencing of the 16S ribosomal RNA gene. The specific amplified sequences were in the V3 and V4 regions of the 16S ribosomal RNA gene. The gut microbiota of RRMS patients differed from healthy controls in the levels of the , , , , , , , , and genera. All these genera were included in a logistic regression analysis to determine the sensitivity and the specificity of the test. Finally, the ROC (receiver operating characteristic) and AUC with a 95% CI were calculated and best-matched for (AUC of 75.0 and CI from 60.6 to 89.4) and (AUC of 70.2 and CI from 50.1 to 90.4). There is a dysbiosis in the gut microbiota of RRMS patients. An analysis of the components of the microbiota suggests the role of some genera as a predictive factor of RRMS prognosis and diagnosis.
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Recent findings have shown a different composition of gut microbiota detected in patients with multiple sclerosis (MS). The role of this dysbiosis is still unknown. We analyzed the gut microbiota of 15 patients with active relapsing-remitting multiple sclerosis (RRMS), comparing with diet-matched healthy controls. To determine the composition of the gut microbiota, we performed high-throughput sequencing of the 16S ribosomal RNA gene. The specific amplified sequences were in the V3 and V4 regions of the 16S ribosomal RNA gene. The gut microbiota of RRMS patients differed from healthy controls in the levels of the , , , , , , , , and genera. All these genera were included in a logistic regression analysis to determine the sensitivity and the specificity of the test. Finally, the ROC (receiver operating characteristic) and AUC with a 95% CI were calculated and best-matched for (AUC of 75.0 and CI from 60.6 to 89.4) and (AUC of 70.2 and CI from 50.1 to 90.4). 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Recent findings have shown a different composition of gut microbiota detected in patients with multiple sclerosis (MS). The role of this dysbiosis is still unknown. We analyzed the gut microbiota of 15 patients with active relapsing-remitting multiple sclerosis (RRMS), comparing with diet-matched healthy controls. To determine the composition of the gut microbiota, we performed high-throughput sequencing of the 16S ribosomal RNA gene. The specific amplified sequences were in the V3 and V4 regions of the 16S ribosomal RNA gene. The gut microbiota of RRMS patients differed from healthy controls in the levels of the , , , , , , , , and genera. All these genera were included in a logistic regression analysis to determine the sensitivity and the specificity of the test. Finally, the ROC (receiver operating characteristic) and AUC with a 95% CI were calculated and best-matched for (AUC of 75.0 and CI from 60.6 to 89.4) and (AUC of 70.2 and CI from 50.1 to 90.4). 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subjects Analysis
Antibiotics
Antigens
Biological markers
Biomarkers
Bowel disease
Brain damage
Care and treatment
Composition
Diagnosis
Dysbacteriosis
Fecal incontinence
Immune system
Intestinal microflora
Lymphocytes
Magnetic resonance imaging
Microbiomes
Microbiota
Microbiota (Symbiotic organisms)
Microorganisms
Multiple sclerosis
Neurological diseases
Next-generation sequencing
Patients
Permeability
Ribosomal RNA
rRNA 16S
Vitamin D
Vitamin deficiency
title Gut Microbiota as a Potential Predictive Biomarker in Relapsing-Remitting Multiple Sclerosis
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