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A framework for optimal whole-sample histological quantification of neurite orientation dispersion in the human spinal cord

Abstract:
The complexity of fibre distributions in tissues is an important microstructural feature, now measurable in vivo by magnetic resonance imaging (MRI) through orientation dispersion (OD) indices. OD metrics have gained popularity for the characterisation of neurite morphology, but they still lack systematic validation. This paper demonstrates a framework for whole-sample histological quantification of OD in spinal cord specimens, potentially useful for validating MRI-derived OD estimates.Our methodological framework is based on (i) sagittal sectioning; (ii) Palmgren's silver staining; (iii) structure tensor (ST) analysis; (iv) directional statistics. Novel elements are the data-driven optimisation of the spatial scale of ST analysis, and a new multivariate, weighted directional statistical approach for anisotropy-informed quantification of OD.Palmgren's silver staining of sagittal spinal cord sections provides robust visualisation of neuronal elements, enabling OD quantification. The choice of spatial scale of ST analysis influences OD values, and weighted directional statistics provide OD maps with high contrast-to-noise. Segmentation of neurites prior to OD quantification is recommended.Our framework can potentially provide OD even in demyelinating diseases, where myelin-based histology is not suitable. As compared to conventional univariate approaches, our multivariate weighted directional statistics improve the contrast-to-noise of OD maps and more accurately describe the distribution of ST metrics.Our framework enables practical whole-specimen characterisation of OD in the spinal cord. We recommend tuning the scale of ST analysis for optimal OD quantification, as well as neurite segmentation and weighted directional statistics, of which examples are provided herein.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.jneumeth.2016.08.002

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Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author


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Grant:
H2020-EU.3.1 CDS-QUAMRI grant (ref: 634541


Publisher:
Elsevier
Journal:
Journal of Neuroscience Methods More from this journal
Publication date:
2016-08-03
Acceptance date:
2016-08-02
DOI:
EISSN:
1872-678X
ISSN:
0165-0270
Pmid:
27497747


Language:
English
Keywords:
Pubs id:
pubs:638338
UUID:
uuid:053b2e2f-9ae9-4ae7-ac29-792e516cd935
Local pid:
pubs:638338
Source identifiers:
638338
Deposit date:
2016-10-09

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