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Microscopic susceptibility anisotropy imaging

PURPOSE: The gradient‐echo MR signal in brain white matter depends on the orientation of the fibers with respect to the external magnetic field. To map microstructure‐specific magnetic susceptibility in orientationally heterogeneous material, it is thus imperative to regress out unwanted orientation...

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Detalles Bibliográficos
Autores principales: Kaden, Enrico, Gyori, Noemi G., Rudrapatna, S. Umesh, Barskaya, Irina Y., Dragonu, Iulius, Does, Mark D., Jones, Derek K., Clark, Chris A., Alexander, Daniel C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402021/
https://www.ncbi.nlm.nih.gov/pubmed/32378746
http://dx.doi.org/10.1002/mrm.28303
Descripción
Sumario:PURPOSE: The gradient‐echo MR signal in brain white matter depends on the orientation of the fibers with respect to the external magnetic field. To map microstructure‐specific magnetic susceptibility in orientationally heterogeneous material, it is thus imperative to regress out unwanted orientation effects. METHODS: This work introduces a novel framework, referred to as microscopic susceptibility anisotropy imaging, that disentangles the 2 principal effects conflated in gradient‐echo measurements, (a) the susceptibility properties of tissue microenvironments, especially the myelin microstructure, and (b) the axon orientation distribution relative to the magnetic field. Specifically, we utilize information about the orientational tissue structure inferred from diffusion MRI data to factor out the [Formula: see text] ‐direction dependence of the frequency difference signal. RESULTS: A human pilot study at 3 T demonstrates proxy maps of microscopic susceptibility anisotropy unconfounded by fiber crossings and orientation dispersion as well as magnetic field direction. The developed technique requires only a dual‐echo gradient‐echo scan acquired at 1 or 2 head orientations with respect to the magnetic field and a 2‐shell diffusion protocol achievable on standard scanners within practical scan times. CONCLUSIONS: The quantitative recovery of microscopic susceptibility features in the presence of orientational heterogeneity potentially improves the assessment of microstructural tissue integrity.