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November 2018; 5 (6) ArticleOpen Access

The MRI central vein marker; differentiating PPMS from RRMS and ischemic SVD

Amal P.R. Samaraweera, Yasser Falah, Alain Pitiot, Robert A. Dineen, Paul S. Morgan, Nikos Evangelou
First published September 26, 2018, DOI: https://doi.org/10.1212/NXI.0000000000000496
Amal P.R. Samaraweera
From the Division of Clinical Neuroscience (A.P.R.S., Y.F., R.A.D., N.E.), University of Nottingham; Laboratory of Image & Data Analysis (A.P.), Ilixa Ltd; National Institute of Health Research (R.A.D.), Nottingham Biomedical Research Centre; and Department of Medical Physics (P.S.M.), Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
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Yasser Falah
From the Division of Clinical Neuroscience (A.P.R.S., Y.F., R.A.D., N.E.), University of Nottingham; Laboratory of Image & Data Analysis (A.P.), Ilixa Ltd; National Institute of Health Research (R.A.D.), Nottingham Biomedical Research Centre; and Department of Medical Physics (P.S.M.), Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
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Alain Pitiot
From the Division of Clinical Neuroscience (A.P.R.S., Y.F., R.A.D., N.E.), University of Nottingham; Laboratory of Image & Data Analysis (A.P.), Ilixa Ltd; National Institute of Health Research (R.A.D.), Nottingham Biomedical Research Centre; and Department of Medical Physics (P.S.M.), Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
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Robert A. Dineen
From the Division of Clinical Neuroscience (A.P.R.S., Y.F., R.A.D., N.E.), University of Nottingham; Laboratory of Image & Data Analysis (A.P.), Ilixa Ltd; National Institute of Health Research (R.A.D.), Nottingham Biomedical Research Centre; and Department of Medical Physics (P.S.M.), Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
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Paul S. Morgan
From the Division of Clinical Neuroscience (A.P.R.S., Y.F., R.A.D., N.E.), University of Nottingham; Laboratory of Image & Data Analysis (A.P.), Ilixa Ltd; National Institute of Health Research (R.A.D.), Nottingham Biomedical Research Centre; and Department of Medical Physics (P.S.M.), Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
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Nikos Evangelou
From the Division of Clinical Neuroscience (A.P.R.S., Y.F., R.A.D., N.E.), University of Nottingham; Laboratory of Image & Data Analysis (A.P.), Ilixa Ltd; National Institute of Health Research (R.A.D.), Nottingham Biomedical Research Centre; and Department of Medical Physics (P.S.M.), Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
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The MRI central vein marker; differentiating PPMS from RRMS and ischemic SVD
Amal P.R. Samaraweera, Yasser Falah, Alain Pitiot, Robert A. Dineen, Paul S. Morgan, Nikos Evangelou
Neurol Neuroimmunol Neuroinflamm Nov 2018, 5 (6) e496; DOI: 10.1212/NXI.0000000000000496

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Abstract

Objective To determine whether the assessment of brain white matter lesion (WML) central veins differentiate patients with primary progressive MS (PPMS) from relapsing-remitting MS (RRMS) and ischemic small vessel disease (SVD) using 3T MRI.

Methods In this cross-sectional study, 71 patients with PPMS, RRMS, and SVD were imaged using a T2*-weighted sequence. Two blinded raters identified the total number of WMLs, proportion of WMLs in periventricular, deep white matter (DWM) and juxtacortical regions, and proportion of WMLs with central veins in all patient groups. The proportions were compared between disease groups, including effect sizes. MS or SVD was categorized using a threshold of ≥40% WMLs with central veins as indicative of MS. Interrater and intrarater reproducibility was calculated.

Results The mean proportion of WMLs with central veins was 68.4% in PPMS, 74.3% in RRMS, and 4.7% in SVD. The difference in proportions between PPMS and SVD groups was significant (p < 0.0005; effect size: 3.8) but not significant between MS subtypes (p = 0.3; effect size: 0.29). Distribution of WMLs was similar across both MS groups, but despite SVD patients having more DWM lesions than PPMS patients, proportions of WMLs with central veins remained low (2.75% in SVD; 62.5% in PPMS). Interrater and intrarater reproducibility comparing proportions of WMLs with central veins across all patients was 0.86 and 0.90, respectively. Level of agreement between the proportion of WML central veins and established diagnosis was 0.84 and 0.82 for each rater.

Conclusions WML central veins could be used to differentiate PPMS from SVD but not between MS subtypes.

Glossary

DWM=
deep white matter;
ICC=
intraclass correlation coefficient;
IQR=
interquartile range;
JC=
juxtacortical;
PPMS=
primary progressive MS;
PV=
periventricular;
RRMS=
relapsing-remitting MS;
SVD=
small vessel disease;
WML=
white matter lesion

Footnotes

  • Funding information and disclosures are provided at the end of the article. Full disclosure form information provided by the authors is available with the full text of this article at Neurology.org/NN.

  • The Article Processing Charge was funded by the authors.

  • Received May 16, 2018.
  • Accepted in final form June 28, 2018.
  • Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.

This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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