Altered intestinal permeability in patients with relapsing–remitting multiple sclerosis: A pilot study

Author:

Buscarinu Maria Chiara1,Cerasoli Benedetta1,Annibali Viviana1,Policano Claudia1,Lionetto Luana2,Capi Matilde3,Mechelli Rosella1,Romano Silvia1,Fornasiero Arianna1,Mattei Gianluca1,Piras Eleonora4,Angelini Daniela Francesca4,Battistini Luca4,Simmaco Maurizio3,Umeton Renato1,Salvetti Marco1,Ristori Giovanni1

Affiliation:

1. Center for Experimental Neurological Therapies, Sant’Andrea Hospital, Department of Neurosciences, Mental Health and Sensory Organs (NESMOS), Faculty of Medicine and Psychology, Sapienza University of Rome, Rome, Italy

2. Advanced Molecular Diagnostics Unit, IDI-IRCCS, Istituto Dermopatico dell’Immacolata, Rome, Italy

3. Department of Neurosciences, Mental Health and Sensory Organs (NESMOS), Faculty of Medicine and Psychology, Sapienza University of Rome, Rome, Italy

4. Neuroimmunology Unit, Fondazione Santa Lucia, Rome, Italy

Abstract

Background: Alterations of intestinal permeability (IP) may contribute to the pathophysiology of immune-mediated diseases. Objective: We investigated the possible association between IP changes and multiple sclerosis (MS). Methods: We studied 22 patients with relapsing–remitting multiple sclerosis (RRMS) and 18 age- and sex-matched healthy donors (HDs), including five twin pairs (one concordant, and four discordant for disease). Measurement of lactulose (L) and mannitol (M; two non-metabolized sugars) levels in urine samples, after an oral load, allowed to quantify gut dysfunction. Results: The proportion of participants with increased IP was significantly higher in patients than in HDs (16/22 (73%) versus 5/18 (28%); p = 0.001). Accordingly, the L/M urinary ratio showed significantly higher values in patients than in controls ( p = 0.0284). Urinary mannitol concentration was significantly lower in patients than in controls ( p = 0.022), suggesting a deficit of absorption from intestinal lumen. Such changes did not appear related to patients’ clinical–radiological features. Conclusion: The relatively high proportion of IP changes in RR-MS patients seems to confirm our work hypothesis and warrants more work to confirm the result on a larger sample, and to understand the implications for related immunological disturbances and intestinal microbiota alterations. Our finding may also have relevance for oral treatments, recently introduced in clinical practice.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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