kth.sePublications KTH
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Machine Learning and Multiparametric Brain MRI to Differentiate Hereditary Diffuse Leukodystrophy with Spheroids from Multiple Sclerosis
Show others and affiliations
2020 (English)In: Journal of Neuroimaging, ISSN 1051-2284, E-ISSN 1552-6569, Vol. 30, no 5, p. 674-682Article in journal (Refereed) Published
Abstract [en]

BACKGROUND AND PURPOSE: Hereditary diffuse leukoencephalopathy with spheroids (HDLS) and multiple sclerosis (MS) are demyelinating and neurodegenerative disorders that can be hard to distinguish clinically and radiologically. HDLS is a rare disorder compared to MS, which has led to occurrent misdiagnosis of HDLS as MS. That is problematic since their prognosis and treatment differ. Both disorders are investigated by MRI, which could help to identify patients with high probability of having HDLS, which could guide targeted genetic testing to confirm the HDLS diagnosis. METHODS: Here, we present a machine learning method based on quantitative MRI that can achieve a robust classification of HDLS versus MS. Four HDLS and 14 age-matched MS patients underwent a quantitative brain MRI protocol (synthetic MRI) at 3 Tesla (T) (scan time '7 minutes). We also performed a repeatability analysis of the predicting features to assess their generalizability by scanning a healthy control with five scan-rescans at 3T and 1.5T. RESULTS: Our predicting features were measured with an average confidence interval of 1.7% (P =.01), at 3T and 2.3% (P =.01) at 1.5T. The model gave a 100% correct classification of the cross-validation data when using 5-11 predicting features. When the maximum measurement noise was inserted in the model, the true positive rate of HDLS was 97.2%, while the true positive rate of MS was 99.6%. CONCLUSIONS: This study suggests that computer-assistance in combination with quantitative MRI may be helpful in aiding the challenging differential diagnosis of HDLS versus MS. 

Place, publisher, year, edition, pages
Blackwell Publishing Inc. , 2020. Vol. 30, no 5, p. 674-682
Keywords [en]
Differential diagnosis, hereditary diffuse leukoencephalopathy with spheroids, multiple sclerosis, quantitative MRI, adult, Article, clinical article, controlled study, cross validation, feature selection, female, genetic screening, hereditary diffuse leukodystrophy, human, leave one out cross validation, leukodystrophy, machine learning, male, middle aged, noise, nuclear magnetic resonance imaging, prospective study, quantitative analysis, volumetry
National Category
Neurology
Identifiers
URN: urn:nbn:se:kth:diva-286470DOI: 10.1111/jon.12725ISI: 000535317300001PubMedID: 32453488Scopus ID: 2-s2.0-85085570283OAI: oai:DiVA.org:kth-286470DiVA, id: diva2:1511016
Note

QC 20201217

Available from: 2020-12-17 Created: 2020-12-17 Last updated: 2024-03-15Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records

Plattén, Michael

Search in DiVA

By author/editor
Plattén, Michael
By organisation
School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH)
In the same journal
Journal of Neuroimaging
Neurology

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 56 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf