Cargando…
7 Tesla Magnetic Resonance Imaging to Detect Cortical Pathology in Multiple Sclerosis
BACKGROUND: Neocortical lesions (NLs) are an important pathological component of multiple sclerosis (MS), but their visualization by magnetic resonance imaging (MRI) remains challenging. OBJECTIVES: We aimed at assessing the sensitivity of multi echo gradient echo (ME-GRE) T(2) (*)-weighted MRI at 7...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4193749/ https://www.ncbi.nlm.nih.gov/pubmed/25303286 http://dx.doi.org/10.1371/journal.pone.0108863 |
Sumario: | BACKGROUND: Neocortical lesions (NLs) are an important pathological component of multiple sclerosis (MS), but their visualization by magnetic resonance imaging (MRI) remains challenging. OBJECTIVES: We aimed at assessing the sensitivity of multi echo gradient echo (ME-GRE) T(2) (*)-weighted MRI at 7.0 Tesla in depicting NLs compared to myelin and iron staining. METHODS: Samples from two MS patients were imaged post mortem using a whole body 7T MRI scanner with a 24-channel receive-only array. Isotropic 200 micron resolution images with varying T(2) (*) weighting were reconstructed from the ME-GRE data and converted into R(2) (*) maps. Immunohistochemical staining for myelin (proteolipid protein, PLP) and diaminobenzidine-enhanced Turnbull blue staining for iron were performed. RESULTS: Prospective and retrospective sensitivities of MRI for the detection of NLs were 48% and 67% respectively. We observed MRI maps detecting only a small portion of 20 subpial NLs extending over large cortical areas on PLP stainings. No MRI signal changes suggestive of iron accumulation in NLs were observed. Conversely, R(2) (*) maps indicated iron loss in NLs, which was confirmed by histological quantification. CONCLUSIONS: High-resolution post mortem imaging using R(2) (*) and magnitude maps permits detection of focal NLs. However, disclosing extensive subpial demyelination with MRI remains challenging. |
---|