Examining brain microstructure using structure tensor analysis of histological sections
NeuroImage, ISSN: 1053-8119, Vol: 63, Issue: 1, Page: 1-10
2012
- 119Citations
- 237Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations119
- Citation Indexes119
- 119
- CrossRef70
- Captures237
- Readers237
- 232
Article Description
The mammalian central nervous system has a tremendous structural complexity, and diffusion tensor imaging (DTI) is unique in its ability to extract microstructural tissue properties at a macroscopic scale. However, despite its widespread use and applications in clinical and research settings, accurate validation of DTI has notoriously lagged the advances in image acquisition and analysis. In this report, we demonstrate an approach to visualize and quantify the microscopic features of histological sections on multiple length scales using techniques derived from image texture analysis. Structure tensor (ST) analysis was applied to fluorescence microscopy images of rat brain sections to visualize and quantify tissue microstructure. Images were digitally color-coded based on the local orientation in the pixelwise ST implementation, which allowed direct visualization of white matter complexity at the microscopic level. A piecewise ST algorithm was also employed to quantify anisotropy and orientation at a resolution comparable to that typically acquired with DTI. Anisotropy measured with ST analysis of stained histological sections was highly correlated with anisotropy measured by ex vivo DTI of the same brains (R 2 = 0.92). Furthermore, angular histograms, or Fiber Orientation Distributions (FODs), were computed to mimic similar measures derived from high angular resolution diffusion imaging methods. The FODs for each pixel were fit to a mixture of von Mises distributions to identify putative regions of multiple fiber populations (i.e. crossing fibers). Despite its current application to two-dimensional microscopy, the ST analysis is a novel approach to visualize and quantify microstructure in the central nervous system in both health and disease, and advances the available set of tools for validating DTI and other diffusion MRI techniques.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S105381191200657X; http://dx.doi.org/10.1016/j.neuroimage.2012.06.042; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84864039331&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/22759994; https://linkinghub.elsevier.com/retrieve/pii/S105381191200657X; https://dx.doi.org/10.1016/j.neuroimage.2012.06.042
Elsevier BV
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