In Vivo Imaging of Tau Pathology Using Magnetic Resonance Imaging Textural Analysis

• Published in: Frontiers in neuroscience Vol. 11; p. 599
• Main Authors: Colgan, Niall, Ganeshan, Balaji, Harrison, Ian F., Ismail, Ozama, Holmes, Holly E., Wells, Jack A., Powell, Nick M., O'Callaghan, James M., O'Neill, Michael J., Murray, Tracey K., Ahmed, Zeshan, Collins, Emily C., Johnson, Ross A., Groves, Ashley, Lythgoe, Mark F.
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 06.11.2017; Frontiers Media S.A
• Subjects: Alzheimer's Disease; Animal cognition; Autism; Cognitive ability; Entropy; Filtration; Hippocampus; Histology; Magnetic resonance imaging; MRI imaging; MRTA; Neuroimaging; Neuroscience; NMR; Nuclear magnetic resonance; Pathology; Schizophrenia; Studies; Tau protein; tauopathies; texture analysis; Thalamus; University colleges; United Kingdom > UK; United States > US; tauopathies; MRI imaging; Alzheimer's Disease; MRTA; texture analysis
• ISSN: 1662-453X; 1662-4548; 1662-453X
• DOI: 10.3389/fnins.2017.00599

Non-invasive characterization of the pathological features of Alzheimer's disease (AD) could enhance patient management and the development of therapeutic strategies. Magnetic resonance imaging texture analysis (MRTA) has been used previously to extract texture descriptors from structural clinical scans in AD to determine cerebral tissue heterogeneity. In this study, we examined the potential of MRTA to specifically identify tau pathology in an AD mouse model and compared the MRTA metrics to histological measures of tau burden. MRTA was applied to T2 weighted high-resolution MR images of nine 8.5-month-old rTg4510 tau pathology (TG) mice and 16 litter matched wild-type (WT) mice. MRTA comprised of the filtration-histogram technique, where the filtration step extracted and enhanced features of different sizes (fine, medium, and coarse texture scales), followed by quantification of texture using histogram analysis (mean gray level intensity, mean intensity, entropy, uniformity, skewness, standard-deviation, and kurtosis). MRTA was applied to manually segmented regions of interest (ROI) drawn within the cortex, hippocampus, and thalamus regions and the level of tau burden was assessed in equivalent regions using histology. Texture parameters were markedly different between WT and TG in the cortex (E, < 0.01, K, < 0.01), the hippocampus (K, < 0.05) and in the thalamus (K, < 0.01). In addition, we observed significant correlations between histological measurements of tau burden and kurtosis in the cortex, hippocampus and thalamus. MRTA successfully differentiated WT and TG in brain regions with varying degrees of tau pathology (cortex, hippocampus, and thalamus) based on T2 weighted MR images. Furthermore, the kurtosis measurement correlated with histological measures of tau burden. This initial study indicates that MRTA may have a role in the early diagnosis of AD and the assessment of tau pathology using routinely acquired structural MR images.