TY - JOUR
T1 - In vivo microstructural heterogeneity of white matter lesions in healthy elderly and Alzheimer's disease participants using tissue compositional analysis of diffusion MRI data
AU - Mito, Remika
AU - Dhollander, Thijs
AU - Xia, Ying
AU - Raffelt, David
AU - Salvado, Olivier
AU - Churilov, Leonid
AU - Rowe, Christopher C.
AU - Brodtmann, Amy
AU - Villemagne, Victor L.
AU - Connelly, Alan
N1 - Funding Information:
We are grateful to the National Health and Medical Research Council (NHMRC) of Australia and the Victorian Government’s Operational Infrastructure Support Program for their funding support. VV is supported by an NHMRC Research Fellowship (1046571). RM is supported by a Melbourne International Research Scholarship from the University of Melbourne and Yulgibar Alzheimer’s Research Program Award.
Funding Information:
We thank the patients, researchers and clinicians involved in the Australian Imaging, Biomarkers, and Lifestyle study of ageing. The Florey Institute of Neuroscience and Mental Health acknowledges the strong support from the Victorian Government and in particular the funding from the Operational Infrastructure Support Grant. The authors acknowledge the facilities and scientific and technical assistance of the National Imaging Facility, a National Collaborative Research Infrastructure Strategy (NCRIS) capability, at the Florey Institute of Neuroscience and Mental Health. We are grateful to the National Health and Medical Research Council (NHMRC) of Australia and the Victorian Government's Operational Infrastructure Support Program for their funding support. VV is supported by an NHMRC Research Fellowship (1046571). RM is supported by a Melbourne International Research Scholarship from the University of Melbourne and Yulgibar Alzheimer's Research Program Award.
Publisher Copyright:
© 2020 The Authors
PY - 2020
Y1 - 2020
N2 - White matter hyperintensities (WMH) are regions of high signal intensity typically identified on fluid attenuated inversion recovery (FLAIR). Although commonly observed in elderly individuals, they are more prevalent in Alzheimer's disease (AD) patients. Given that WMH appear relatively homogeneous on FLAIR, they are commonly partitioned into location- or distance-based classes when investigating their relevance to disease. Since pathology indicates that such lesions are often heterogeneous, probing their microstructure in vivo may provide greater insight than relying on such arbitrary classification schemes. In this study, we investigated WMH in vivo using an advanced diffusion MRI method known as single-shell 3-tissue constrained spherical deconvolution (SS3T-CSD), which models white matter microstructure while accounting for grey matter and CSF compartments. Diffusion MRI data and FLAIR images were obtained from AD (n = 48) and healthy elderly control (n = 94) subjects. WMH were automatically segmented, and classified: (1) as either periventricular or deep; or (2) into three distance-based contours from the ventricles. The 3-tissue profile of WMH enabled their characterisation in terms of white matter-, grey matter-, and fluid-like characteristics of the diffusion signal. Our SS3T-CSD findings revealed substantial heterogeneity in the 3-tissue profile of WMH, both within lesions and across the various classes. Moreover, this heterogeneity information indicated that the use of different commonly used WMH classification schemes can result in different disease-based conclusions. We conclude that future studies of WMH in AD would benefit from inclusion of microstructural information when characterising lesions, which we demonstrate can be performed in vivo using SS3T-CSD.
AB - White matter hyperintensities (WMH) are regions of high signal intensity typically identified on fluid attenuated inversion recovery (FLAIR). Although commonly observed in elderly individuals, they are more prevalent in Alzheimer's disease (AD) patients. Given that WMH appear relatively homogeneous on FLAIR, they are commonly partitioned into location- or distance-based classes when investigating their relevance to disease. Since pathology indicates that such lesions are often heterogeneous, probing their microstructure in vivo may provide greater insight than relying on such arbitrary classification schemes. In this study, we investigated WMH in vivo using an advanced diffusion MRI method known as single-shell 3-tissue constrained spherical deconvolution (SS3T-CSD), which models white matter microstructure while accounting for grey matter and CSF compartments. Diffusion MRI data and FLAIR images were obtained from AD (n = 48) and healthy elderly control (n = 94) subjects. WMH were automatically segmented, and classified: (1) as either periventricular or deep; or (2) into three distance-based contours from the ventricles. The 3-tissue profile of WMH enabled their characterisation in terms of white matter-, grey matter-, and fluid-like characteristics of the diffusion signal. Our SS3T-CSD findings revealed substantial heterogeneity in the 3-tissue profile of WMH, both within lesions and across the various classes. Moreover, this heterogeneity information indicated that the use of different commonly used WMH classification schemes can result in different disease-based conclusions. We conclude that future studies of WMH in AD would benefit from inclusion of microstructural information when characterising lesions, which we demonstrate can be performed in vivo using SS3T-CSD.
KW - 3-tissue
KW - Alzheimer's disease
KW - Diffusion MRI
KW - Heterogeneity
KW - White matter hyperintensities
UR - https://www.scopus.com/pages/publications/85095408716
U2 - 10.1016/j.nicl.2020.102479
DO - 10.1016/j.nicl.2020.102479
M3 - Article
C2 - 33395971
AN - SCOPUS:85095408716
SN - 2213-1582
VL - 28
JO - NeuroImage: Clinical
JF - NeuroImage: Clinical
M1 - 102479
ER -