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The MRI central vein marker; differentiating PPMS from RRMS and ischemic SVD
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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192690/ https://www.ncbi.nlm.nih.gov/pubmed/30345329 http://dx.doi.org/10.1212/NXI.0000000000000496 |
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author | Samaraweera, Amal P.R. Falah, Yasser Pitiot, Alain Dineen, Robert A. Morgan, Paul S. Evangelou, Nikos |
author_facet | Samaraweera, Amal P.R. Falah, Yasser Pitiot, Alain Dineen, Robert A. Morgan, Paul S. Evangelou, Nikos |
author_sort | Samaraweera, Amal P.R. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6192690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-61926902018-10-19 The MRI central vein marker; differentiating PPMS from RRMS and ischemic SVD Samaraweera, Amal P.R. Falah, Yasser Pitiot, Alain Dineen, Robert A. Morgan, Paul S. Evangelou, Nikos Neurol Neuroimmunol Neuroinflamm Article 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. Lippincott Williams & Wilkins 2018-09-26 /pmc/articles/PMC6192690/ /pubmed/30345329 http://dx.doi.org/10.1212/NXI.0000000000000496 Text en 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) (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Samaraweera, Amal P.R. Falah, Yasser Pitiot, Alain Dineen, Robert A. Morgan, Paul S. Evangelou, Nikos The MRI central vein marker; differentiating PPMS from RRMS and ischemic SVD |
title | The MRI central vein marker; differentiating PPMS from RRMS and ischemic SVD |
title_full | The MRI central vein marker; differentiating PPMS from RRMS and ischemic SVD |
title_fullStr | The MRI central vein marker; differentiating PPMS from RRMS and ischemic SVD |
title_full_unstemmed | The MRI central vein marker; differentiating PPMS from RRMS and ischemic SVD |
title_short | The MRI central vein marker; differentiating PPMS from RRMS and ischemic SVD |
title_sort | mri central vein marker; differentiating ppms from rrms and ischemic svd |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192690/ https://www.ncbi.nlm.nih.gov/pubmed/30345329 http://dx.doi.org/10.1212/NXI.0000000000000496 |
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