Study the Longitudinal in vivo and Cross-Sectional ex vivo Brain Volume Difference for Disease Progression and Treatment Effect on Mouse Model of Tauopathy Using Automated MRI Structural Parcellation
Brain volume measurements extracted from structural MRI data sets are a widely accepted neuroimaging biomarker to study mouse models of neurodegeneration. Whether to acquire and analyze data or is a crucial decision during the phase of experimental designs, as well as data analysis. In this work, we...
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Veröffentlicht in: | Frontiers in neuroscience 2019-01, Vol.13, p.11-11 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Brain volume measurements extracted from structural MRI data sets are a widely accepted neuroimaging biomarker to study mouse models of neurodegeneration. Whether to acquire and analyze data
or
is a crucial decision during the phase of experimental designs, as well as data analysis. In this work, we extracted the brain structures for both longitudinal
and single-time-point
MRI acquired from the same animals using accurate automatic multi-atlas structural parcellation, and compared the corresponding statistical and classification analysis. We found that most gray matter structures volumes decrease from
to
, while most white matter structures volume increase. The level of structural volume change also varies between different genetic strains and treatment. In addition, we showed superior statistical and classification power of
data compared to the
data, even after resampled to the same level of resolution. We further demonstrated that the classification power of the
data can be improved by incorporating longitudinal information, which is not possible for
data. In conclusion, this paper demonstrates the tissue-specific changes, as well as the difference in statistical and classification power, between the volumetric analysis based on the
and
structural MRI data. Our results emphasize the importance of longitudinal analysis for
data analysis. |
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ISSN: | 1662-4548 1662-453X 1662-453X |
DOI: | 10.3389/fnins.2019.00011 |