Dynamics of pseudo-atrophy in RRMS reveals predominant gray matter compartmentalization.


Journal

Annals of clinical and translational neurology
ISSN: 2328-9503
Titre abrégé: Ann Clin Transl Neurol
Pays: United States
ID NLM: 101623278

Informations de publication

Date de publication:
03 2021
Historique:
received: 03 09 2020
revised: 19 11 2020
accepted: 27 12 2020
pubmed: 4 2 2021
medline: 3 11 2021
entrez: 3 2 2021
Statut: ppublish

Résumé

To assess the dynamics of "pseudo-atrophy," the accelerated brain volume loss observed after initiation of anti-inflammatory therapies, in patients with multiple sclerosis (MS). Monthly magnetic resonance imaging (MRI) data of patients from the IMPROVE clinical study (NCT00441103) comparing relapsing-remitting MS patients treated with interferon beta-1a (IFNβ-1a) for 40 weeks versus those receiving placebo (16 weeks) and then IFNβ-1a (24 weeks) were used to assess percentage of gray (PGMVC) and white matter (PWMVC) volume changes. Comparisons of PGMVC and PWMVC slopes were performed with a mixed effect linear model. In the IFNβ-1a-treated arm, a quadratic term was included in the model to evaluate the plateauing effect over 40 weeks. Up to week 16, PGMVC was -0.14% per month in the placebo and -0.27% per month in treated patients (P < 0.001). Over the same period, the decrease in PWMVC was -0.067% per month in the placebo and -0.116% per month in treated patients (P = 0.27). Similar changes were found in the group originally randomized to placebo when starting IFNβ-1a treatment (week 16-40, reliability analysis). In the originally treated group, over 40 weeks, the decrease in PGMVC showed a significant (P < 0.001) quadratic component, indicating a plateauing at week 20. Findings reported here add new insights into the complex mechanisms of pseudo-atrophy and its relation to the compartmentalized inflammation occurring in the GM of MS patients. Ongoing and forthcoming clinical trials including MRI-derived GM volume loss as an outcome measure need to account for potentially significant GM volume changes as part of the initial treatment effect.

Identifiants

pubmed: 33534940
doi: 10.1002/acn3.51302
pmc: PMC7951094
doi:

Substances chimiques

Immunologic Factors 0
Interferon beta-1a XRO4566Q4R

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

623-630

Informations de copyright

© 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.

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Auteurs

Nicola De Stefano (N)

Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.

Antonio Giorgio (A)

Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.

Giordano Gentile (G)

Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.

Maria Laura Stromillo (ML)

Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.

Rosa Cortese (R)

Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.

Claudio Gasperini (C)

San Camillo-Forlanini Hospital, Rome, Italy.

Andrea Visconti (A)

Medical Affairs Department, Merck Serono, Rome, Italy.

Maria Pia Sormani (MP)

Biostatistics Unit, Department of Health Sciences, University of Genoa, Genoa, Italy.

Marco Battaglini (M)

Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.

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Classifications MeSH