Abstract

Progressive multifocal leukoencephalopathy (PML) is a severe complication of immunosuppressive therapies, especially of natalizumab in relapsing-remitting multiple sclerosis (MS). Metabolic changes within PML lesions have not yet been described in natalizumab-associated PML in MS patients. To study metabolic profiles in natalizumab-associated PML lesions of MS patients by 1H magnetic resonance spectroscopy (1H-MRS) at different stages during the PML course. To assess changes associated with the occurrence of the immune reconstitution inflammatory syndrome (IRIS). 20 patients received 1H-MRS and imaging at 3 T either in the pre-IRIS, IRIS, early-post-PML, or late post-PML setting. Five of these patients received individual follow-up examinations, including the pre-IRIS or IRIS phase. Clinical worsening was described by changes in the Karnofsky Performance Scale (KPS) and the expanded disability status scale (EDSS) 1 year before PML and scoring at the time of 1H-MRS. In PML lesions, increased levels of the Lip/Cr ratio, driven by rising of lipid and reduction of Creatine, were found before the occurrence of IRIS (p = 0.014) with a maximum in the PML-IRIS group (p = 0.004). By contrast, marked rises of Cho/Cr in PML lesions were detected exclusively during the IRIS phase (p = 0.003). The Lip/Cr ratio decreased to above-normal levels in early-post-PML (p = 0.007, compared to normal appearing white matter (NAWM)) and to normal levels in the late-post-PML group. NAA/Cho was reduced compared to NAWM in the pre-IRIS, IRIS, and early-post-PML group. In NAA/Cr, the same effect was seen in the pre-IRIS and early-post-PML group. These cross-sectional results were confirmed by the individual follow-up examinations of four patients. NAA/Cho, Cho/Cr, and the lipid rise relative to NAWM in PML lesions were significantly correlated with the residual clinical worsening (KPS change) in post-PML patients (Spearman correlations ρ = 0.481, p = 0.018; ρ = -0.505, p = 0.014; and ρ = -0.488, p = 0.020). 1H-MRS detected clinically significant dynamic changes of metabolic patterns in PML lesions during the course of natalizumab-associated PML in MS patients. Lip/Cr and Cho/Cr may provide additional information for detecting the onset of the IRIS phase in the course of the PML disease.

Highlights

  • Progressive multifocal leukoencephalopathy (PML) occurs in immunocompromised patients as an opportunistic infection of the central nervous system caused by the John Cunningham Virus (JCV)

  • The individual PML lesion presentation in conventional Magnetic resonance imaging (MRI) at the time of MRS compared to the situation at PML diagnosis and PML–immune reconstitution inflammatory syndrome (IRIS) was assessed

  • The PML lesions were hypointense on unenhanced T1 weighted images in most of the cases except three patients in the pre-IRIS and early IRIS phase

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Summary

Introduction

Progressive multifocal leukoencephalopathy (PML) occurs in immunocompromised patients as an opportunistic infection of the central nervous system caused by the John Cunningham Virus (JCV). Patients with a human immunodeficiency virus (HIV) infection are mainly affected [1], but it occurs as a rare side effect in natalizumab-treated patients with relapsing–remitting multiple sclerosis (RR-MS) [2]. Even though there are limited data for the prognostic value of MRI regarding the clinical outcome of PML patients, higher survival rates could be demonstrated in more localized manifestations of the disease (unilobar and multilobar brain involvement) in contrast to widespread PML attack within the brain’s white matter [7, 8]. Progressive multifocal leukoencephalopathy (PML) is a severe complication of immunosuppressive therapies, especially of natalizumab in relapsing–remitting multiple sclerosis (MS). Metabolic changes within PML lesions have not yet been described in natalizumab-associated PML in MS patients

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