•  Home
  • Library
  • DRO home
Submit research Contact DRO

DRO

Openly accessible

MRI Patterns Distinguish AQP4 Antibody Positive Neuromyelitis Optica Spectrum Disorder From Multiple Sclerosis

Clarke, L, Arnett, S, Bukhari, W, Khalilidehkordi, E, Jimenez Sanchez, S, O'Gorman, C, Sun, J, Prain, KM, Woodhall, M, Silvestrini, R, Bundell, CS, Abernethy, DA, Bhuta, S, Blum, S, Boggild, M, Boundy, K, Brew, BJ, Brownlee, W, Butzkueven, H, Carroll, WM, Chen, C, Coulthard, A, Dale, RC, Das, C, Fabis-Pedrini, MJ, Gillis, D, Hawke, S, Heard, R, Henderson, APD, Heshmat, S, Hodgkinson, S, Kilpatrick, TJ, King, J, Kneebone, C, Kornberg, AJ, Lechner-Scott, J, Lin, MW, Lynch, C, Macdonell, RAL, Mason, DF, McCombe, PA, Pereira, J, Pollard, JD, Ramanathan, S, Reddel, SW, Shaw, Cameron, Spies, JM, Stankovich, J, Sutton, I, Vucic, S, Walsh, M, Wong, RC, Yiu, EM, Barnett, MH, Kermode, AGK, Marriott, MP, Parratt, JDE, Slee, M, Taylor, BV, Willoughby, E, Brilot, F, Vincent, A, Waters, P and Broadley, SA 2021, MRI Patterns Distinguish AQP4 Antibody Positive Neuromyelitis Optica Spectrum Disorder From Multiple Sclerosis, Frontiers in Neurology, vol. 12, pp. 1-24, doi: 10.3389/fneur.2021.722237.

Attached Files
Name Description MIMEType Size Downloads

Title MRI Patterns Distinguish AQP4 Antibody Positive Neuromyelitis Optica Spectrum Disorder From Multiple Sclerosis
Author(s) Clarke, L
Arnett, S
Bukhari, W
Khalilidehkordi, E
Jimenez Sanchez, S
O'Gorman, C
Sun, J
Prain, KM
Woodhall, M
Silvestrini, R
Bundell, CS
Abernethy, DA
Bhuta, S
Blum, S
Boggild, M
Boundy, K
Brew, BJ
Brownlee, W
Butzkueven, H
Carroll, WM
Chen, C
Coulthard, A
Dale, RC
Das, C
Fabis-Pedrini, MJ
Gillis, D
Hawke, S
Heard, R
Henderson, APD
Heshmat, S
Hodgkinson, S
Kilpatrick, TJ
King, J
Kneebone, C
Kornberg, AJ
Lechner-Scott, J
Lin, MW
Lynch, C
Macdonell, RAL
Mason, DF
McCombe, PA
Pereira, J
Pollard, JD
Ramanathan, S
Reddel, SW
Shaw, CameronORCID iD for Shaw, Cameron orcid.org/0000-0002-1966-5200
Spies, JM
Stankovich, J
Sutton, I
Vucic, S
Walsh, M
Wong, RC
Yiu, EM
Barnett, MH
Kermode, AGK
Marriott, MP
Parratt, JDE
Slee, M
Taylor, BV
Willoughby, E
Brilot, F
Vincent, A
Waters, P
Broadley, SA
Journal name Frontiers in Neurology
Volume number 12
Article ID 722237
Start page 1
End page 24
Total pages 24
Publisher Frontiers
Place of publication Lausanne, Switzerland
Publication date 2021-09
ISSN 1664-2295
1664-2295
Keyword(s) BRAIN ABNORMALITIES
Clinical Neurology
CLINICALLY ISOLATED SYNDROMES
diagnosis
EXTENSIVE TRANSVERSE MYELITIS
FOLLOW-UP
INFLAMMATORY DEMYELINATING DISORDERS
Life Sciences & Biomedicine
magnetic resonance imaging
MATTER INVOLVEMENT
multiple sclerosis
neuromyelitis optica
Neurosciences
Neurosciences & Neurology
NMOSD
PREDICT CONVERSION
RESONANCE-IMAGING FINDINGS
REVERSIBLE ENCEPHALOPATHY SYNDROME
Science & Technology
SPINAL-CORD LESIONS
Summary Neuromyelitis optica spectrum disorder (NMOSD) and multiple sclerosis (MS) are inflammatory diseases of the CNS. Overlap in the clinical and MRI features of NMOSD and MS means that distinguishing these conditions can be difficult. With the aim of evaluating the diagnostic utility of MRI features in distinguishing NMOSD from MS, we have conducted a cross-sectional analysis of imaging data and developed predictive models to distinguish the two conditions. NMOSD and MS MRI lesions were identified and defined through a literature search. Aquaporin-4 (AQP4) antibody positive NMOSD cases and age- and sex-matched MS cases were collected. MRI of orbits, brain and spine were reported by at least two blinded reviewers. MRI brain or spine was available for 166/168 (99%) of cases. Longitudinally extensive (OR = 203), “bright spotty” (OR = 93.8), whole (axial; OR = 57.8) or gadolinium (Gd) enhancing (OR = 28.6) spinal cord lesions, bilateral (OR = 31.3) or Gd-enhancing (OR = 15.4) optic nerve lesions, and nucleus tractus solitarius (OR = 19.2), periaqueductal (OR = 16.8) or hypothalamic (OR = 7.2) brain lesions were associated with NMOSD. Ovoid (OR = 0.029), Dawson's fingers (OR = 0.031), pyramidal corpus callosum (OR = 0.058), periventricular (OR = 0.136), temporal lobe (OR = 0.137) and T1 black holes (OR = 0.154) brain lesions were associated with MS. A score-based algorithm and a decision tree determined by machine learning accurately predicted more than 85% of both diagnoses using first available imaging alone. We have confirmed NMOSD and MS specific MRI features and combined these in predictive models that can accurately identify more than 85% of cases as either AQP4 seropositive NMOSD or MS
Language eng
DOI 10.3389/fneur.2021.722237
Field of Research 1103 Clinical Sciences
1109 Neurosciences
1701 Psychology
HERDC Research category C1 Refereed article in a scholarly journal
Free to Read? Yes
Persistent URL http://hdl.handle.net/10536/DRO/DU:30156480

Document type: Journal Article
Collections: Faculty of Health
School of Medicine
Open Access Collection
Related Links
Link Description
Link to full-text (open access)  
Connect to Elements publication management system
Go to link with your DU access privileges
 
Connect to link resolver
 
Unless expressly stated otherwise, the copyright for items in DRO is owned by the author, with all rights reserved.

Every reasonable effort has been made to ensure that permission has been obtained for items included in DRO. If you believe that your rights have been infringed by this repository, please contact drosupport@deakin.edu.au.

Versions
Version Filter Type
Citation counts: TR Web of Science Citation Count  Cited 0 times in TR Web of Science
Scopus Citation Count Cited 1 times in Scopus Google Scholar Search Google Scholar
Access Statistics: 29 Abstract Views, 0 File Downloads  -  Detailed Statistics
Created: Wed, 06 Oct 2021, 07:10:59 EST

Every reasonable effort has been made to ensure that permission has been obtained for items included in DRO. If you believe that your rights have been infringed by this repository, please contact drosupport@deakin.edu.au.