HACA3: A unified approach for multi-site MR image harmonization.


Journal

Computerized medical imaging and graphics : the official journal of the Computerized Medical Imaging Society
ISSN: 1879-0771
Titre abrégé: Comput Med Imaging Graph
Pays: United States
ID NLM: 8806104

Informations de publication

Date de publication:
10 2023
Historique:
received: 11 05 2023
revised: 11 07 2023
accepted: 08 08 2023
pmc-release: 01 10 2024
medline: 23 10 2023
pubmed: 2 9 2023
entrez: 1 9 2023
Statut: ppublish

Résumé

The lack of standardization and consistency of acquisition is a prominent issue in magnetic resonance (MR) imaging. This often causes undesired contrast variations in the acquired images due to differences in hardware and acquisition parameters. In recent years, image synthesis-based MR harmonization with disentanglement has been proposed to compensate for the undesired contrast variations. The general idea is to disentangle anatomy and contrast information from MR images to achieve cross-site harmonization. Despite the success of existing methods, we argue that major improvements can be made from three aspects. First, most existing methods are built upon the assumption that multi-contrast MR images of the same subject share the same anatomy. This assumption is questionable, since different MR contrasts are specialized to highlight different anatomical features. Second, these methods often require a fixed set of MR contrasts for training (e.g., both T1-weighted and T2-weighted images), limiting their applicability. Lastly, existing methods are generally sensitive to imaging artifacts. In this paper, we present Harmonization with Attention-based Contrast, Anatomy, and Artifact Awareness (HACA3), a novel approach to address these three issues. HACA3 incorporates an anatomy fusion module that accounts for the inherent anatomical differences between MR contrasts. Furthermore, HACA3 can be trained and applied to any combination of MR contrasts and is robust to imaging artifacts. HACA3 is developed and evaluated on diverse MR datasets acquired from 21 sites with varying field strengths, scanner platforms, and acquisition protocols. Experiments show that HACA3 achieves state-of-the-art harmonization performance under multiple image quality metrics. We also demonstrate the versatility and potential clinical impact of HACA3 on downstream tasks including white matter lesion segmentation for people with multiple sclerosis and longitudinal volumetric analyses for normal aging subjects. Code is available at https://github.com/lianruizuo/haca3.

Identifiants

pubmed: 37657151
pii: S0895-6111(23)00103-9
doi: 10.1016/j.compmedimag.2023.102285
pmc: PMC10592042
mid: NIHMS1928578
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

102285

Subventions

Organisme : NIA NIH HHS
ID : P30 AG066507
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS082347
Pays : United States
Organisme : Intramural NIH HHS
ID : Z99 AG999999
Pays : United States

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Jerry Prince, Aaron Carass, Peter Calabresi reports financial support was provided by National Institutes of Health. Ellen Mowry, Scott Newsome, Jerry Prince, Aaron Carass reports financial support was provided by Patient-Centered Outcomes Research Institute. Jerry Prince, Aaron Carass reports financial support was provided by US Office of Congressionally Directed Medical Research Programs. Blake Dewey reports financial support was provided by National Multiple Sclerosis Society. Jerry Prince reports a relationship with Sonavex that includes: board membership, consulting or advisory, and equity or stocks.

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Auteurs

Lianrui Zuo (L)

Department of Electrical and Computer Engineering, Johns Hopkins University, Baltimore, MD 21218, USA; Laboratory of Behavioral Neuroscience, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA. Electronic address: lr_zuo@jhu.edu.

Yihao Liu (Y)

Department of Electrical and Computer Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.

Yuan Xue (Y)

Department of Electrical and Computer Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.

Blake E Dewey (BE)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.

Samuel W Remedios (SW)

Department of Computer Science, Johns Hopkins University, Baltimore, MD 21218, USA; Radiology and Imaging Sciences, Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA.

Savannah P Hays (SP)

Department of Electrical and Computer Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.

Murat Bilgel (M)

Laboratory of Behavioral Neuroscience, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.

Ellen M Mowry (EM)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.

Scott D Newsome (SD)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.

Peter A Calabresi (PA)

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.

Susan M Resnick (SM)

Laboratory of Behavioral Neuroscience, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.

Jerry L Prince (JL)

Department of Electrical and Computer Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.

Aaron Carass (A)

Department of Electrical and Computer Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.

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