Quantitative MRI outcome measures in CMT1A using automated lower limb muscle segmentation.

MRI NEUROPATHY

Journal

Journal of neurology, neurosurgery, and psychiatry
ISSN: 1468-330X
Titre abrégé: J Neurol Neurosurg Psychiatry
Pays: England
ID NLM: 2985191R

Informations de publication

Date de publication:
18 Nov 2023
Historique:
received: 18 08 2023
accepted: 25 10 2023
medline: 19 11 2023
pubmed: 19 11 2023
entrez: 18 11 2023
Statut: aheadofprint

Résumé

Lower limb muscle magnetic resonance imaging (MRI) obtained fat fraction (FF) can detect disease progression in patients with Charcot-Marie-Tooth disease 1A (CMT1A). However, analysis is time-consuming and requires manual segmentation of lower limb muscles. We aimed to assess the responsiveness, efficiency and accuracy of acquiring FF MRI using an artificial intelligence-enabled automated segmentation technique. We recruited 20 CMT1A patients and 7 controls for assessment at baseline and 12 months. The three-point-Dixon fat water separation technique was used to determine thigh-level and calf-level muscle FF at a single slice using regions of interest defined using Musclesense, a trained artificial neural network for lower limb muscle image segmentation. A quality control (QC) check and correction of the automated segmentations was undertaken by a trained observer. The QC check took on average 30 seconds per slice to complete. Using QC checked segmentations, the mean calf-level FF increased significantly in CMT1A patients from baseline over an average follow-up of 12.5 months (1.15%±1.77%, paired t-test p=0.016). Standardised response mean (SRM) in patients was 0.65. Without QC checks, the mean FF change between baseline and follow-up, at 1.15%±1.68% (paired t-test p=0.01), was almost identical to that seen in the corrected data, with a similar overall SRM at 0.69. Using automated image segmentation for the first time in a longitudinal study in CMT, we have demonstrated that calf FF has similar responsiveness to previously published data, is efficient with minimal time needed for QC checks and is accurate with minimal corrections needed.

Sections du résumé

BACKGROUND BACKGROUND
Lower limb muscle magnetic resonance imaging (MRI) obtained fat fraction (FF) can detect disease progression in patients with Charcot-Marie-Tooth disease 1A (CMT1A). However, analysis is time-consuming and requires manual segmentation of lower limb muscles. We aimed to assess the responsiveness, efficiency and accuracy of acquiring FF MRI using an artificial intelligence-enabled automated segmentation technique.
METHODS METHODS
We recruited 20 CMT1A patients and 7 controls for assessment at baseline and 12 months. The three-point-Dixon fat water separation technique was used to determine thigh-level and calf-level muscle FF at a single slice using regions of interest defined using Musclesense, a trained artificial neural network for lower limb muscle image segmentation. A quality control (QC) check and correction of the automated segmentations was undertaken by a trained observer.
RESULTS RESULTS
The QC check took on average 30 seconds per slice to complete. Using QC checked segmentations, the mean calf-level FF increased significantly in CMT1A patients from baseline over an average follow-up of 12.5 months (1.15%±1.77%, paired t-test p=0.016). Standardised response mean (SRM) in patients was 0.65. Without QC checks, the mean FF change between baseline and follow-up, at 1.15%±1.68% (paired t-test p=0.01), was almost identical to that seen in the corrected data, with a similar overall SRM at 0.69.
CONCLUSIONS CONCLUSIONS
Using automated image segmentation for the first time in a longitudinal study in CMT, we have demonstrated that calf FF has similar responsiveness to previously published data, is efficient with minimal time needed for QC checks and is accurate with minimal corrections needed.

Identifiants

pubmed: 37979968
pii: jnnp-2023-332454
doi: 10.1136/jnnp-2023-332454
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: HZ has served at scientific advisory boards and/or as a consultant for Abbvie, Acumen, Alector, Alzinova, ALZPath, Annexon, Apellis, Artery Therapeutics, AZTherapies, CogRx, Denali, Eisai, Nervgen, Novo Nordisk, Optoceutics, Passage Bio, Pinteon Therapeutics, Prothena, Red Abbey Labs, reMYND, Roche, Samumed, Siemens Healthineers, Triplet Therapeutics and Wave, has given lectures in symposia sponsored by Cellectricon, Fujirebio, Alzecure, Biogen and Roche, and is a cofounder of Brain Biomarker Solutions in Gothenburg AB (BBS), which is a part of the GU Ventures Incubator Program (outside submitted work).

Auteurs

Luke F O'Donnell (LF)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

Menelaos Pipis (M)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

John S Thornton (JS)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

Baris Kanber (B)

UCL Centre for Medical Image Computing, London, UK.

Stephen Wastling (S)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

Amy McDowell (A)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

Nick Zafeiropoulos (N)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

Matilde Laura (M)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

Mariola Skorupinska (M)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

Christopher J Record (CJ)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

Carolynne M Doherty (CM)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

David N Herrmann (DN)

Department of Neurology, University of Rochester, Rochester, New York, USA.

Henrik Zetterberg (H)

Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, UK.
UK Dementia Research Institute at UCL, London, UK.

Amanda J Heslegrave (AJ)

Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, UK.
UK Dementia Research Institute at UCL, London, UK.

Rhiannon Laban (R)

UK Dementia Research Institute at UCL, London, UK.

Alexander M Rossor (AM)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

Jasper M Morrow (JM)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

Mary M Reilly (MM)

Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK m.reilly@ucl.ac.uk.

Classifications MeSH