Journal Article DZNE-2021-00654

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Optical coherence tomography angiography indicates subclinical retinal disease in neuromyelitis optica spectrum disorders.

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2022
Sage London

Multiple sclerosis journal 28(4), 522-531 () [10.1177/13524585211028831]

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Abstract: Neuromyelitis optica spectrum disorders (NMOSD) are neuroinflammatory diseases of the central nervous system. Patients suffer from recurring relapses and it is unclear whether relapse-independent disease activity occurs and whether this is of clinical relevance.To detect disease-specific alterations of the retinal vasculature that reflect disease activity during NMOSD.Cross-sectional analysis of 16 patients with NMOSD, 21 patients with relapsing-remitting multiple sclerosis, and 21 healthy controls using retinal optical coherence tomography (OCT), optical coherence tomography angiography (OCT-A), measurement of glial fibrillary acidic protein (GFAP) serum levels, and assessment of visual acuity.Patients with NMOSD but not multiple sclerosis revealed lower foveal thickness (FT) (p = 0.02) measures and an increase of the foveal avascular zone (FAZ) (p = 0.02) compared to healthy controls independent to optic neuritis. Reduced FT (p = 0.01), enlarged FAZ areas (p = 0.0001), and vessel loss of the superficial vascular complex (p = 0.01) were linked to higher serum GFAP levels and superficial vessel loss was associated with worse visual performance in patients with NMOSD irrespective of optic neuritis.Subclinical parafoveal retinal vessel loss might occur during NMOSD and might be linked to astrocyte damage and poor visual performance. OCT-A may be a tool to study subclinical disease activity during NMOSD.

Keyword(s): Angiography (MeSH) ; Cross-Sectional Studies (MeSH) ; Humans (MeSH) ; Neuromyelitis Optica: diagnosis (MeSH) ; Retinal Diseases (MeSH) ; Tomography, Optical Coherence: methods (MeSH) ; Neuromyelitis optica spectrum disorders ; astrocytes ; biomarker ; disease activity ; optical coherence tomography angiography

Classification:

Contributing Institute(s):
  1. Molecular Neurodegeneration (AG Haass)
Research Program(s):
  1. 352 - Disease Mechanisms (POF4-352) (POF4-352)

Appears in the scientific report 2022
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Medline ; Creative Commons Attribution CC BY 4.0 ; OpenAccess ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; Current Contents - Life Sciences ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 5 ; JCR ; National-Konsortium ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2021-08-12, last modified 2024-03-02


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