Diffusion MRI harmonization enables joint-analysis of multicentre data of patients with cerebral small vessel disease.


Journal

NeuroImage. Clinical
ISSN: 2213-1582
Titre abrégé: Neuroimage Clin
Pays: Netherlands
ID NLM: 101597070

Informations de publication

Date de publication:
2021
Historique:
received: 21 10 2021
accepted: 16 11 2021
entrez: 16 12 2021
pubmed: 17 12 2021
medline: 20 1 2022
Statut: ppublish

Résumé

Acquisition-related differences in diffusion magnetic resonance imaging (dMRI) hamper pooling of multicentre data to achieve large sample sizes. A promising solution is to harmonize the raw diffusion signal using rotation invariant spherical harmonic (RISH) features, but this has not been tested in elderly subjects. Here we aimed to establish if RISH harmonization effectively removes acquisition-related differences in multicentre dMRI of elderly subjects with cerebral small vessel disease (SVD), while preserving sensitivity to disease effects. Five cohorts of patients with SVD (N = 397) and elderly controls (N = 175) with 3 Tesla MRI on different systems were included. First, to establish effectiveness of harmonization, the RISH method was trained with data of 13 to 15 age and sex-matched controls from each site. Fractional anisotropy (FA) and mean diffusivity (MD) were compared in matched controls between sites using tract-based spatial statistics (TBSS) and voxel-wise analysis, before and after harmonization. Second, to assess sensitivity to disease effects, we examined whether the contrast (effect sizes of FA, MD and peak width of skeletonized MD - PSMD) between patients and controls within each site remained unaffected by harmonization. Finally, we evaluated the association between white matter hyperintensity (WMH) burden, FA, MD and PSMD using linear regression analyses both within individual cohorts as well as with pooled scans from multiple sites, before and after harmonization. Before harmonization, significant differences in FA and MD were observed between matched controls of different sites (p < 0.05). After harmonization these site-differences were removed. Within each site, RISH harmonization did not alter the effect sizes of FA, MD and PSMD between patients and controls (relative change in Cohen's d = 4 %) nor the strength of association with WMH volume (relative change in R We showed that RISH harmonization effectively removes acquisition-related differences in dMRI of elderly subjects while preserving sensitivity to SVD-related effects. This study provides proof of concept for future multicentre SVD studies with pooled datasets.

Identifiants

pubmed: 34911192
pii: S2213-1582(21)00330-2
doi: 10.1016/j.nicl.2021.102886
pmc: PMC8609094
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

102886

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Bruno M de Brito Robalo (BM)

Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands; Image Sciences Institute, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands. Electronic address: B.M.deBritoRobalo-2@umcutrecht.nl.

Geert Jan Biessels (GJ)

Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands. Electronic address: G.J.Biessels@umcutrecht.nl.

Christopher Chen (C)

Memory, Aging and Cognition Center, Department of Pharmacology, National University of Singapore, Singapore. Electronic address: phccclh@nus.edu.sg.

Anna Dewenter (A)

Institute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, Germany. Electronic address: Anna.Dewenter@med.uni-muenchen.de.

Marco Duering (M)

Institute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, Germany; Medical Image Analysis Center (MIAC AG) and qbig, Department of Biomedical Engineering, University of Basel, Basel, Switzerland. Electronic address: marco.duering@miac.ch.

Saima Hilal (S)

Memory, Aging and Cognition Center, Department of Pharmacology, National University of Singapore, Singapore. Electronic address: saimahilal@nus.edu.sg.

Huiberdina L Koek (HL)

Department of Geriatric Medicine, University Medical Center Utrecht, Utrecht, The Netherlands. Electronic address: H.L.Koek@umcutrecht.nl.

Anna Kopczak (A)

Institute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, Germany. Electronic address: Anna.Kopczak@med.uni-muenchen.de.

Bonnie Yin Ka Lam (B)

Division of Neurology, Department of Medicine and Therapeutics, Gerald Choa Neuroscience Centre, Faculty of Medicine, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong Special Administrative Region. Electronic address: bonnieyklam@cuhk.edu.hk.

Alexander Leemans (A)

Image Sciences Institute, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands. Electronic address: A.Leemans@umcutrecht.nl.

Vincent Mok (V)

Division of Neurology, Department of Medicine and Therapeutics, Gerald Choa Neuroscience Centre, Faculty of Medicine, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong Special Administrative Region. Electronic address: vctmok@cuhk.edu.hk.

Laurien P Onkenhout (LP)

Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands. Electronic address: L.P.Onkenhout@umcutrecht.nl.

Hilde van den Brink (H)

Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands. Electronic address: H.vandenBrink-2@umcutrecht.nl.

Alberto de Luca (A)

Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands; Image Sciences Institute, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands. Electronic address: A.deLuca-2@umcutrecht.nl.

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