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Eur Radiol. 2016 Dec;26(12):4413-4422. Epub 2016 Mar 24.

Brain parenchymal damage in neuromyelitis optica spectrum disorder - A multimodal MRI study.

Author information

1
NeuroCure Clinical Research Center and Experimental and Clinical Research Center, Max Delbrueck Center for Molecular Medicine and Charité- Universitätsmedizin Berlin, Berlin, Germany. florence.pache@charite.de.
2
Department of Neurology, Charité- Universitätsmedizin Berlin, Berlin, Germany. florence.pache@charite.de.
3
NeuroCure Clinical Research Center and Experimental and Clinical Research Center, Max Delbrueck Center for Molecular Medicine and Charité- Universitätsmedizin Berlin, Berlin, Germany.
4
Department of Neurology, Charité- Universitätsmedizin Berlin, Berlin, Germany.
5
Berlin School of Mind and Brain, Humboldt-Universitaet zu Berlin, Berlin, Germany.
6
Department of Radiology, Charité- Universitätsmedizin Berlin, Berlin, Germany.

Abstract

OBJECTIVE:

To investigate different brain regions for grey (GM) and white matter (WM) damage in a well-defined cohort of neuromyelitis optica spectrum disorder (NMOSD) patients and compare advanced MRI techniques (VBM, Subcortical and cortical analyses (Freesurfer), and DTI) for their ability to detect damage in NMOSD.

METHODS:

We analyzed 21 NMOSD patients and 21 age and gender matched control subjects. VBM (GW/WM) and DTI whole brain (TBSS) analyses were performed at different statistical thresholds to reflect different statistical approaches in previous studies. In an automated atlas-based approach, Freesurfer and DTI results were compared between NMOSD and controls.

RESULTS:

DTI TBSS and DTI atlas based analysis demonstrated microstructural impairment only within the optic radiation or in regions associated with the optic radiation (posterior thalamic radiation p < 0.001, 6.9 % reduction of fractional anisotropy). VBM demonstrated widespread brain GM and WM reduction, but only at exploratory statistical thresholds, with no differences remaining after correction for multiple comparisons. Freesurfer analysis demonstrated no group differences.

CONCLUSION:

NMOSD specific parenchymal brain damage is predominantly located in the optic radiation, likely due to a secondary degeneration caused by ON. In comparison, DTI appears to be the most reliable and sensitive technique for brain damage detection in NMOSD.

KEY POINTS:

• The hypothesis of a widespread brain damage in NMOSD is challenged. • The optic radiation (OR) is the most severely affected region. • OR-affection is likely due to secondary degeneration following optic neuritis. • DTI is currently the most sensitive technique for NMOSD-related brain-damage detection. • DTI is currently the most reliable technique for NMOSD-related brain-damage detection.

KEYWORDS:

Demyelination; Diffusion tensor Imaging; Neuromyelitis optica spectrum disorder; Optical coherence tomography; VBM analysis

PMID:
27012555
DOI:
10.1007/s00330-016-4282-x
[Indexed for MEDLINE]

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