Literature DB >> 27864579

Automated segmentation reveals silent radiographic progression in adult-onset vanishing white-matter disease.

Thomas Huber1, Marina Herwerth2, Esther Alberts1, Jan S Kirschke1, Claus Zimmer1, Ruediger Ilg2,3.   

Abstract

Adult-onset vanishing white-matter disease (VWM) is a rare autosomal recessive disease with neurological symptoms such as ataxia and paraparesis, showing extensive white-matter hyperintensities (WMH) on magnetic resonance (MR) imaging. Besides symptom-specific scores like the International Cooperative Ataxia Rating Scale (ICARS), there is no established tool to monitor disease progression. Because of extensive WMH, visual comparison of MR images is challenging. Here, we report the results of an automated method of segmentation to detect alterations in T2-weighted fluid-attenuated-inversion-recovery (FLAIR) sequences in a one-year follow-up study of a clinically stable patient with genetically diagnosed VWM. Signal alterations in MR imaging were quantified with a recently published WMH segmentation method by means of extreme value distribution (EVD). Our analysis revealed progressive FLAIR alterations of 5.84% in the course of one year, whereas no significant WMH change could be detected in a stable multiple sclerosis (MS) control group. This result demonstrates that automated EVD-based segmentation allows a precise and rapid quantification of extensive FLAIR alterations like in VWM and might be a powerful tool for the clinical and scientific monitoring of degenerative white-matter diseases and potential therapeutic interventions.

Entities:  

Keywords:  Extreme value distribution; automated segmentation; vanishing white-matter disease; white-matter hyperintensities

Mesh:

Substances:

Year:  2016        PMID: 27864579      PMCID: PMC5564332          DOI: 10.1177/1971400916678222

Source DB:  PubMed          Journal:  Neuroradiol J        ISSN: 1971-4009


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4.  Imaging evidence of early brain tissue degeneration in patients with vanishing white matter disease: a multimodal MR study.

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5.  Adult-onset vanishing white matter disease as differential diagnosis of primary progressive multiple sclerosis: a case report.

Authors:  Marina Herwerth; Benedikt J Schwaiger; Kornelia Kreiser; Bernhard Hemmer; Rüdiger Ilg
Journal:  Mult Scler       Date:  2014-08-18       Impact factor: 6.312

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7.  Natural history of adult-onset eIF2B-related disorders: a multi-centric survey of 16 cases.

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9.  A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation.

Authors:  Laura Ghezzi; Elio Scarpini; Mario Rango; Andrea Arighi; Maria Teresa Bassi; Erika Tenderini; Milena De Riz; Francesca Jacini; Giorgio G Fumagalli; Anna M Pietroboni; Daniela Galimberti; Nereo Bresolin
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10.  The life and death of oligodendrocytes in vanishing white matter disease.

Authors:  Keith Van Haren; J Patrick van der Voorn; Derick R Peterson; Marjo S van der Knaap; James M Powers
Journal:  J Neuropathol Exp Neurol       Date:  2004-06       Impact factor: 3.685

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  2 in total

1.  Similarities and differences between infantile and early childhood onset vanishing white matter disease.

Authors:  Ling Zhou; Haihua Zhang; Na Chen; Zhongbin Zhang; Ming Liu; Lifang Dai; Jingmin Wang; Yuwu Jiang; Ye Wu
Journal:  J Neurol       Date:  2018-04-16       Impact factor: 4.849

Review 2.  Genotypic and phenotypic characteristics of juvenile/adult onset vanishing white matter: a series of 14 Chinese patients.

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Journal:  Neurol Sci       Date:  2022-04-07       Impact factor: 3.830

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