High-efficacy therapy reduces subcortical grey matter volume loss in Japanese patients with relapse-onset multiple sclerosis: A 2-year cohort study.


Journal

Multiple sclerosis and related disorders
ISSN: 2211-0356
Titre abrégé: Mult Scler Relat Disord
Pays: Netherlands
ID NLM: 101580247

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 03 02 2022
revised: 14 07 2022
accepted: 24 07 2022
pubmed: 5 8 2022
medline: 10 11 2022
entrez: 4 8 2022
Statut: ppublish

Résumé

Different treatment strategies can have varying effects on disability and whole brain volume in patients with multiple sclerosis (MS). However, the association between regional brain volume and treatment efficacy is currently unclear. Our objective was to determine whether whole brain volume, as well as the regional volume of cortical and subcortical grey matter, differ with the administration of high-efficacy therapy (HET) versus low-efficacy therapy (LET). We evaluated clinical data and change in regional brain volume in 44 patients with relapse-onset MS, who underwent HET (n = 19) or LET (n = 25). Regional brain volume was determined with three-dimensional T1-weighted magnetic resonance imaging using FreeSurfer. The association between volume change and treatment type was assessed via generalised linear mixed models (GLMMs). During the observation period (2.0 ± 0.16 years), the proportion of patients with a "no evidence of disease activity-3″ status was significantly greater in those who underwent HET versus LET (p = 0.012). HET was positively associated with volume changes in the cortex (β = 0.64, p = 0.0499), left (β = 0.98, p = 0.0033) and right (β = 0.77, p = 0.019) caudate and right putamen (β = 0.87, p = 0.0077), after adjusting for age, sex, and MS severity scores in the GLMMs. Further correction for multiple comparisons by false discovery rate revealed that HET was consistently associated with the volume changes of the left caudate (p = 0.049) and right putamen (p = 0.049). HET can improve the mid-term prognosis of Japanese patients with relapse-onset MS by reducing disease activity and regional brain volume loss.

Sections du résumé

BACKGROUND BACKGROUND
Different treatment strategies can have varying effects on disability and whole brain volume in patients with multiple sclerosis (MS). However, the association between regional brain volume and treatment efficacy is currently unclear. Our objective was to determine whether whole brain volume, as well as the regional volume of cortical and subcortical grey matter, differ with the administration of high-efficacy therapy (HET) versus low-efficacy therapy (LET).
METHODS METHODS
We evaluated clinical data and change in regional brain volume in 44 patients with relapse-onset MS, who underwent HET (n = 19) or LET (n = 25). Regional brain volume was determined with three-dimensional T1-weighted magnetic resonance imaging using FreeSurfer. The association between volume change and treatment type was assessed via generalised linear mixed models (GLMMs).
RESULTS RESULTS
During the observation period (2.0 ± 0.16 years), the proportion of patients with a "no evidence of disease activity-3″ status was significantly greater in those who underwent HET versus LET (p = 0.012). HET was positively associated with volume changes in the cortex (β = 0.64, p = 0.0499), left (β = 0.98, p = 0.0033) and right (β = 0.77, p = 0.019) caudate and right putamen (β = 0.87, p = 0.0077), after adjusting for age, sex, and MS severity scores in the GLMMs. Further correction for multiple comparisons by false discovery rate revealed that HET was consistently associated with the volume changes of the left caudate (p = 0.049) and right putamen (p = 0.049).
CONCLUSION CONCLUSIONS
HET can improve the mid-term prognosis of Japanese patients with relapse-onset MS by reducing disease activity and regional brain volume loss.

Identifiants

pubmed: 35926261
pii: S2211-0348(22)00585-5
doi: 10.1016/j.msard.2022.104077
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104077

Informations de copyright

Copyright © 2022. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest Hiroaki Yokote has received honoraria for lectures from Biogen, Mitsubishi-Tanabe Pharma, Alexion Pharma Godo Kaisha, Chugai Pharma, and Novartis. Yusei Miyazaki has received honoraria for lectures from Biogen, Alexion Pharma Godo Kaisha, Chugai Pharma and Novartis. Yoichiro Nishida has received honoraria for lectures from Alexion Pharma Godo Kaisha. Masaaki Niino has received speaker honoraria from Novartis Pharma, Biogen Japan, Mitsubishi Tanabe Pharma, Takeda Pharmaceutical Company, and Alexion Pharma Godo Kaisha. Nobuo Sanjo received honoraria for lectures from Takeda, Biogen, and Novartis. Takanori Yokota has received personal fees from Mitsubishi Tanabe Pharma and Takeda, outside the submitted work; Takanori Yokota has a patent Takeda with royalties paid. The other authors declare that they have no competing interests.

Auteurs

Hiroaki Yokote (H)

Department of Neurology, Nitobe Memorial Nakano General Hospital, 4-59-16, Chuo, Nakano-ku, Tokyo 164-8607, Japan; Department of Neurology and Neurological Science, Tokyo Medical and Dental University, Tokyo, Japan. Electronic address: yktenuro@tmd.ac.jp.

Yusei Miyazaki (Y)

Department of Clinical Research, National Hospital Organization Hokkaido Medical Center, Sapporo, Japan.

Shuta Toru (S)

Department of Neurology, Nitobe Memorial Nakano General Hospital, 4-59-16, Chuo, Nakano-ku, Tokyo 164-8607, Japan.

Yoichiro Nishida (Y)

Department of Neurology and Neurological Science, Tokyo Medical and Dental University, Tokyo, Japan.

Takaaki Hattori (T)

Department of Neurology and Neurological Science, Tokyo Medical and Dental University, Tokyo, Japan.

Masaaki Niino (M)

Department of Clinical Research, National Hospital Organization Hokkaido Medical Center, Sapporo, Japan.

Nobuo Sanjo (N)

Department of Neurology and Neurological Science, Tokyo Medical and Dental University, Tokyo, Japan.

Takanori Yokota (T)

Department of Neurology and Neurological Science, Tokyo Medical and Dental University, Tokyo, Japan.

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