TY - JOUR
T1 - Higher-resolution quantification of white matter hypointensities by large-scale transfer learning from 2D images on the JPSC-AD cohort
AU - Japan Prospective Studies Collaboration for Aging and Dementia (JPSC-AD) Study Group
AU - Thyreau, Benjamin
AU - Tatewaki, Yasuko
AU - Chen, Liying
AU - Takano, Yuji
AU - Hirabayashi, Naoki
AU - Furuta, Yoshihiko
AU - Hata, Jun
AU - Nakaji, Shigeyuki
AU - Maeda, Tetsuya
AU - Noguchi-Shinohara, Moeko
AU - Mimura, Masaru
AU - Nakashima, Kenji
AU - Mori, Takaaki
AU - Takebayashi, Minoru
AU - Ninomiya, Toshiharu
AU - Taki, Yasuyuki
N1 - Publisher Copyright:
© 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.
PY - 2022/9
Y1 - 2022/9
N2 - White matter lesions (WML) commonly occur in older brains and are quantifiable on MRI, often used as a biomarker in Aging research. Although algorithms are regularly proposed that identify these lesions from T2-fluid-attenuated inversion recovery (FLAIR) sequences, none so far can estimate lesions directly from T1-weighted images with acceptable accuracy. Since 3D T1 is a polyvalent and higher-resolution sequence, it could be beneficial to obtain the distribution of WML directly from it. However a serious difficulty, both for algorithms and human, can be found in the ambiguities of brain signal intensity in T1 images. This manuscript shows that a cross-domain ConvNet (Convolutional Neural Network) approach can help solve this problem. Still, this is non-trivial, as it would appear to require a large and varied dataset (for robustness) labelled at the same high resolution (for spatial accuracy). Instead, our model was taught from two-dimensional FLAIR images with a loss function designed to handle the super-resolution need. And crucially, we leveraged a very large training set for this task, the recently assembled, multi-sites Japan Prospective Studies Collaboration for Aging and Dementia (JPSC-AD) cohort. We describe the two-step procedure that we followed to handle such a large number of imperfectly labeled samples. A large-scale accuracy evaluation conducted against FreeSurfer 7, and a further visual expert rating revealed that WML segmentation from our ConvNet was consistently better. Finally, we made a directly usable software program based on that trained ConvNet model, available at https://github.com/bthyreau/deep-T1-WMH.
AB - White matter lesions (WML) commonly occur in older brains and are quantifiable on MRI, often used as a biomarker in Aging research. Although algorithms are regularly proposed that identify these lesions from T2-fluid-attenuated inversion recovery (FLAIR) sequences, none so far can estimate lesions directly from T1-weighted images with acceptable accuracy. Since 3D T1 is a polyvalent and higher-resolution sequence, it could be beneficial to obtain the distribution of WML directly from it. However a serious difficulty, both for algorithms and human, can be found in the ambiguities of brain signal intensity in T1 images. This manuscript shows that a cross-domain ConvNet (Convolutional Neural Network) approach can help solve this problem. Still, this is non-trivial, as it would appear to require a large and varied dataset (for robustness) labelled at the same high resolution (for spatial accuracy). Instead, our model was taught from two-dimensional FLAIR images with a loss function designed to handle the super-resolution need. And crucially, we leveraged a very large training set for this task, the recently assembled, multi-sites Japan Prospective Studies Collaboration for Aging and Dementia (JPSC-AD) cohort. We describe the two-step procedure that we followed to handle such a large number of imperfectly labeled samples. A large-scale accuracy evaluation conducted against FreeSurfer 7, and a further visual expert rating revealed that WML segmentation from our ConvNet was consistently better. Finally, we made a directly usable software program based on that trained ConvNet model, available at https://github.com/bthyreau/deep-T1-WMH.
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U2 - 10.1002/hbm.25899
DO - 10.1002/hbm.25899
M3 - Article
C2 - 35524684
AN - SCOPUS:85133837812
SN - 1065-9471
VL - 43
SP - 3998
EP - 4012
JO - Human Brain Mapping
JF - Human Brain Mapping
IS - 13
ER -