Axonal water fraction as marker of white matter injury in primary-progressive multiple sclerosis: a longitudinal study.


Journal

European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311

Informations de publication

Date de publication:
08 2019
Historique:
received: 07 10 2018
accepted: 05 02 2019
pubmed: 15 2 2019
medline: 8 8 2020
entrez: 15 2 2019
Statut: ppublish

Résumé

Diffuse white matter (WM) injury is prominent in primary-progressive multiple sclerosis (PP-MS) pathology and is a potential biomarker of disease progression. Diffusion kurtosis imaging allows the quantification of non-Gaussian water diffusion, providing metrics with high WM pathological specificity. The aim of this study was to characterize the pathological changes occurring in the normal-appearing WM of patients with PP-MS at baseline and at 1-year follow-up and to assess their impact on disability and short-term disease progression. A total of 26 patients with PP-MS and 20 healthy controls were prospectively enrolled. Diffusion kurtosis imaging single-shot echo-planar imaging (EPI) was acquired on a 3-T scanner (Philips Achieva, Best, The Netherlands) (voxel size, 2 × 2 × 2 mm At baseline, patients with PP-MS showed a widespread decrease of AWF, tortuosity and D Based on its change over time and its relationship with disease progression, among the analyzed metrics, AWF seems the most sensitive metric of WM tissue damage in PP-MS and therefore it could be considered as a marker for monitoring disease progression.

Sections du résumé

BACKGROUND AND PURPOSE
Diffuse white matter (WM) injury is prominent in primary-progressive multiple sclerosis (PP-MS) pathology and is a potential biomarker of disease progression. Diffusion kurtosis imaging allows the quantification of non-Gaussian water diffusion, providing metrics with high WM pathological specificity. The aim of this study was to characterize the pathological changes occurring in the normal-appearing WM of patients with PP-MS at baseline and at 1-year follow-up and to assess their impact on disability and short-term disease progression.
METHODS
A total of 26 patients with PP-MS and 20 healthy controls were prospectively enrolled. Diffusion kurtosis imaging single-shot echo-planar imaging (EPI) was acquired on a 3-T scanner (Philips Achieva, Best, The Netherlands) (voxel size, 2 × 2 × 2 mm
RESULTS
At baseline, patients with PP-MS showed a widespread decrease of AWF, tortuosity and D
CONCLUSION
Based on its change over time and its relationship with disease progression, among the analyzed metrics, AWF seems the most sensitive metric of WM tissue damage in PP-MS and therefore it could be considered as a marker for monitoring disease progression.

Identifiants

pubmed: 30761708
doi: 10.1111/ene.13937
doi:

Substances chimiques

Biomarkers 0
Water 059QF0KO0R

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1068-1074

Informations de copyright

© 2019 EAN.

Auteurs

M Margoni (M)

Multiple Sclerosis Centre, Department of Neuroscience DNS, University Hospital, University of Padua, Padua, Italy.
Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

M Petracca (M)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

S Schiavi (S)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics and Maternal and Perinatal Sciences, University of Genoa, Genoa.
IRCSS Azienda Ospedale Università San Martino-IST, Genoa, Italy.

M Fabian (M)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

A Miller (A)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

F D Lublin (FD)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

M Inglese (M)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics and Maternal and Perinatal Sciences, University of Genoa, Genoa.
IRCSS Azienda Ospedale Università San Martino-IST, Genoa, Italy.
Department of Radiology and Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

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