Neuromyelitis optica does not impact periventricular venous density versus healthy controls: a 7.0 Tesla MRI clinical study
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
R01 NS029029
NINDS NIH HHS - United States
R01 NS076588
NINDS NIH HHS - United States
PubMed
27072685
DOI
10.1007/s10334-016-0554-3
PII: 10.1007/s10334-016-0554-3
Knihovny.cz E-zdroje
- Klíčová slova
- 7T MRI, Multiple sclerosis, Neuromyelitis optica, Ultrahigh-field MRI, Venous density,
- MeSH
- dospělí MeSH
- kohortové studie MeSH
- lidé středního věku MeSH
- lidé MeSH
- magnetická rezonanční tomografie * MeSH
- mladý dospělý MeSH
- mozek diagnostické zobrazování patologie MeSH
- neuromyelitis optica diagnostické zobrazování patologie MeSH
- roztroušená skleróza diagnostické zobrazování patologie MeSH
- senioři MeSH
- studie případů a kontrol MeSH
- vény diagnostické zobrazování patologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
OBJECTIVE: To quantify the periventricular venous density in neuromyelitis optica spectrum disease (NMOSD) in comparison to that in patients with multiple sclerosis (MS) and healthy control subjects. MATERIALS AND METHODS: Sixteen patients with NMOSD, 16 patients with MS and 16 healthy control subjects underwent 7.0-Tesla (7T) MRI. The imaging protocol included T2*-weighted (T2*w) fast low angle-shot (FLASH) and fluid-attenuated inversion recovery (FLAIR) sequences. The periventricular venous area (PVA) was manually determined by a blinded investigator in order to estimate the periventricular venous density in a region of interest-based approach. RESULTS: No significant differences in periventricular venous density indicated by PVA were detectable in NMOSD versus healthy controls (p = 0.226). In contrast, PVA was significantly reduced in MS patients compared to healthy controls (p = 0.013). CONCLUSION: Unlike patients with MS, those suffering from NMOSD did not show reduced venous visibility. This finding may underscore primary and secondary pathophysiological differences between these two distinct diseases of the central nervous system.
Berlin Ultrahigh Field Facility Max Delbrück Center for Molecular Medicine Berlin Germany
Department of Neurology Asklepios Fachklinikum Teupitz Teupitz Germany
Department of Neurology Charité Universitätsmedizin Berlin Berlin Germany
Department of Neurology Multiple Sclerosis Care Center NYU School of Medicine New York NY USA
Department of Neurology Universitätsspital Basel Basel Switzerland
Department of Radiology NYU School of Medicine New York NY USA
Institute of Neuroradiology Universitätsmedizin Göttingen Göttingen Germany
Medical Image Analysis Center AG Basel Switzerland
NeuroCure Clinical Research Center Charité Universitätsmedizin Berlin Berlin Germany
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