Literature DB >> 26756564

Hereditary diffuse leukoencephalopathy with spheroids - a volumetric and radiological comparison with multiple sclerosis patients and healthy controls.

T Granberg1,2, F Hashim1,2, O Andersen3, C Sundal3,4, V D Karrenbauer5,6.   

Abstract

BACKGROUND AND
PURPOSE: Hereditary diffuse leukoencephalopathy with spheroids (HDLS) is an autosomal dominant disorder caused by colony-stimulating factor 1 receptor (CSF1R) gene mutations, resulting in demyelination and axonal degeneration with spheroids. The clinical expression is variable, including behavioral changes, cognitive impairment, motor symptoms and parkinsonism. Magnetic resonance imaging (MRI) reveals white matter (WM) changes and atrophy. The indistinct phenotype has led to misdiagnoses. This study's aim was to compare brain volumetry and radiological ratings in HDLS with multiple sclerosis (MS) patients and controls.
METHODS: Five HDLS patients with c.2562T>A p.Asn854Lys CSF1R mutation, five age- and gender-matched MS patients and five healthy controls were cross-sectionally studied. All patients were examined neurologically. HDLS patients underwent Mini-Mental State Examination (MMSE). Brain MRI scans were analyzed volumetrically with FreeSurfer and Lesion Segmentation Toolbox and neuroradiologically with the brain MRI scoring system for HDLS.
RESULTS: Patients with HDLS had lower brain, grey matter and WM fractions (66.3%; 37.9%; 27.6%) compared with controls (78.5%, P = 0.008; 44.4%, P = 0.008; 32.0%, P = 0.008), but not compared with MS patients (65.7%, P = 0.7; 36.8%, P = 0.4; 27.3%, P = 0.7). Cerebellar WM changes and atrophy were not seen in the HDLS group. The HDLS lesion volume fraction correlated with MMSE scores (r = -0.90, P = 0.04).
CONCLUSIONS: Brain volume fractions in HDLS were lower than in controls and similar to those seen in MS. The cerebellum was relatively spared in HDLS, which may help in differentiating HDLS WM changes from MS. The strong relationship of HDLS lesions with MMSE scores indicates that accumulating WM pathology in HDLS is associated with cognitive decline.
© 2016 EAN.

Entities:  

Keywords:  CSF1R; MRI; hereditary diffuse leukoencephalopathy with spheroids; multiple sclerosis; volumetry

Mesh:

Year:  2016        PMID: 26756564     DOI: 10.1111/ene.12948

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  7 in total

1.  Diagnostic Value of Brain Calcifications in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia.

Authors:  T Konno; D F Broderick; N Mezaki; A Isami; D Kaneda; Y Tashiro; T Tokutake; B M Keegan; B K Woodruff; T Miura; H Nozaki; M Nishizawa; O Onodera; Z K Wszolek; T Ikeuchi
Journal:  AJNR Am J Neuroradiol       Date:  2016-09-15       Impact factor: 3.825

2.  Altered intrinsic brain activity in patients with CSF1R-related leukoencephalopathy.

Authors:  Jingying Wu; Yikang Cao; Mengting Li; Binyin Li; Xize Jia; Li Cao
Journal:  Brain Imaging Behav       Date:  2022-04-07       Impact factor: 3.224

Review 3.  Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): update on molecular genetics.

Authors:  Carmen Stabile; Ilaria Taglia; Carla Battisti; Silvia Bianchi; Antonio Federico
Journal:  Neurol Sci       Date:  2016-06-23       Impact factor: 3.307

4.  Identification of a de novo splicing mutation in the CSF1R gene in a Chinese patient with hereditary diffuse leukoencephalopathy with spheroids.

Authors:  Xinwei Wu; Congcong Sun; Xingbang Wang; Ying Liu; Wei Wu; Guoyong Jia
Journal:  Neurol Sci       Date:  2021-11-18       Impact factor: 3.830

Review 5.  Brain Parenchymal Fraction in Healthy Adults-A Systematic Review of the Literature.

Authors:  Mattias Vågberg; Gabriel Granåsen; Anders Svenningsson
Journal:  PLoS One       Date:  2017-01-17       Impact factor: 3.240

Review 6.  Microglial replacement therapy: a potential therapeutic strategy for incurable CSF1R-related leukoencephalopathy.

Authors:  Jinming Han; Heela Sarlus; Zbigniew K Wszolek; Virginija Danylaité Karrenbauer; Robert A Harris
Journal:  Acta Neuropathol Commun       Date:  2020-12-07       Impact factor: 7.801

7.  Four Swedish cases of CSF1R-related leukoencephalopathy: Visualization of clinical phenotypes.

Authors:  Igal Rosenstein; Oluf Andersen; Daniel Victor; Elisabet Englund; Tobias Granberg; Carola Hedberg-Oldfors; Katarina Jood; Yusran Ady Fitrah; Takeshi Ikeuchi; Virginija Danylaité Karrenbauer
Journal:  Acta Neurol Scand       Date:  2022-02-04       Impact factor: 3.915

  7 in total

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