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 - Funding Information:
We would like to thank all researchers and investigators in the JPSC-AD Study Group for their diligent work and contribution. We would like to additionally thank participants for volunteering their time to take part in the JPSC-AD study. Participating institutes and principal collaborators for the JPSC-AD Study group: Kyushu University ([Epidemiology and Public Health] Toshiharu Ninomiya, Jun Hata, Mao Shibata, and Takanori Honda, [Neuropsychiatry] Tomoyuki Ohara, [Pathology and Imaging Science] Masato Akiyama); Hirosaki University (Shigeyuki Nakaji, Koichi Murashita, Tatsuya Mikami, Songee Jung, and Mina Misawa); Iwate Medical University (Tetsuya Maeda, Naoki Ishizuka, and Hiroshi Akasaka); Shonan Keiiku Hospital (Yasuo Terayama); Japanese Red Cross Morioka Hospital (Hisashi Yonezawa); Morioka Tsunagi Onsen Hospital (Junko Takahashi); Kanazawa University (Moeko Noguchi-Shinohara, Masahito Yamada, Kazuo Iwasa, Sohshi Yuki-Nozaki, and Kenjiro Ono); Keio University School of Medicine (Masaru Mimura, Shogyoku Bun, Hidehito Niimura, Ryo Shikimoto, and Hisashi Kida); Matsue Medical Center (Kenji Nakashima, Yasuyo Fukada, and Hisanori Kowa); Kawasaki Medical School (Kenji Wada); Tottori Prefectural Kousei Hospital (Masafumi Kishi); Ehime University (Takaaki Mori, Yuta Yoshino, Hideaki Shimizu, Ayumi Tachibana, and Shu-ichi Ueno); Kumamoto University (Minoru Takebayashi, Tomohisa Ishikawa, Ryuji Fukuhara, and Asuka Koyama); Osaka University Medical School (Mamoru Hashimoto and Manabu Ikeda); National Cerebral and Cardiovascular Center) (Yoshihiro Kokubo); Nakamura-Gakuen University (Kazuhiro Uchida, and Midori Esaki); Tohoku University (Yasuyuki Taki, Yuji Takano, Yasuko Tatewaki, and Benjamin Thyreau);University of the Ryukyu (Koji Yonemoto); Osaka City University Graduate School of Medicine (Hisako Yoshida); University of Tokyo (Kaori Muto, Yusuke Inoue); RIKEN Center for Integrative Medical Sciences (Yukihide Momozawa and Chikashi Terao); Hisayama Research Institute for Lifestyle Diseases (Michiaki Kubo and Yutaka Kiyohara).
Funding Information:
The JPSC‐AD study was supported by the Japan Agency for Medical Research and Development (JP21dk0207053) and Suntory Holdings Limited (Osaka, Japan). The funders had no role in the design of the study, the collection, analysis, and interpretation of data, or the writing of the manuscript.
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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UR - http://www.scopus.com/inward/citedby.url?scp=85133837812&partnerID=8YFLogxK
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 -