TY - JOUR
T1 - Weakly Supervised Deep Learning for Brain Disease Prognosis Using MRI and Incomplete Clinical Scores
AU - Liu, Mingxia
AU - Zhang, Jun
AU - Lian, Chunfeng
AU - Shen, Dinggang
N1 - Funding Information:
Manuscript received November 15, 2018; revised February 3, 2019; accepted March 7, 2019. Date of publication March 26, 2019; date of current version June 16, 2020. This work was supported in part by NIH under Grant EB006733, Grant EB008374, Grant EB009634, Grant MH100217, Grant AG041721, Grant AG042599, Grant AG010129, and Grant AG030514. This paper was recommended by Associate Editor D. Goldgof. (Mingxia Liu and Jun Zhang contributed equally to this work.) (Corresponding author: Dinggang Shen.) M. Liu, J. Zhang, and C. Lian are with the Department of Radiology and BRIC, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599 USA.
Publisher Copyright:
© 2013 IEEE.
PY - 2020/7
Y1 - 2020/7
N2 - As a hot topic in brain disease prognosis, predicting clinical measures of subjects based on brain magnetic resonance imaging (MRI) data helps to assess the stage of pathology and predict future development of the disease. Due to incomplete clinical labels/scores, previous learning-based studies often simply discard subjects without ground-truth scores. This would result in limited training data for learning reliable and robust models. Also, existing methods focus only on using hand-crafted features (e.g., image intensity or tissue volume) of MRI data, and these features may not be well coordinated with prediction models. In this paper, we propose a weakly supervised densely connected neural network (wiseDNN) for brain disease prognosis using baseline MRI data and incomplete clinical scores. Specifically, we first extract multiscale image patches (located by anatomical landmarks) from MRI to capture local-to-global structural information of images, and then develop a weakly supervised densely connected network for task-oriented extraction of imaging features and joint prediction of multiple clinical measures. A weighted loss function is further employed to make full use of all available subjects (even those without ground-truth scores at certain time-points) for network training. The experimental results on 1469 subjects from both ADNI-1 and ADNI-2 datasets demonstrate that our proposed method can efficiently predict future clinical measures of subjects.
AB - As a hot topic in brain disease prognosis, predicting clinical measures of subjects based on brain magnetic resonance imaging (MRI) data helps to assess the stage of pathology and predict future development of the disease. Due to incomplete clinical labels/scores, previous learning-based studies often simply discard subjects without ground-truth scores. This would result in limited training data for learning reliable and robust models. Also, existing methods focus only on using hand-crafted features (e.g., image intensity or tissue volume) of MRI data, and these features may not be well coordinated with prediction models. In this paper, we propose a weakly supervised densely connected neural network (wiseDNN) for brain disease prognosis using baseline MRI data and incomplete clinical scores. Specifically, we first extract multiscale image patches (located by anatomical landmarks) from MRI to capture local-to-global structural information of images, and then develop a weakly supervised densely connected network for task-oriented extraction of imaging features and joint prediction of multiple clinical measures. A weighted loss function is further employed to make full use of all available subjects (even those without ground-truth scores at certain time-points) for network training. The experimental results on 1469 subjects from both ADNI-1 and ADNI-2 datasets demonstrate that our proposed method can efficiently predict future clinical measures of subjects.
KW - Alzheimer's disease (AD)
KW - clinical score
KW - disease prognosis
KW - neural network
KW - weakly supervised learning
UR - http://www.scopus.com/inward/record.url?scp=85075695222&partnerID=8YFLogxK
U2 - 10.1109/TCYB.2019.2904186
DO - 10.1109/TCYB.2019.2904186
M3 - Article
C2 - 30932861
AN - SCOPUS:85075695222
SN - 2168-2267
VL - 50
SP - 3381
EP - 3392
JO - IEEE Transactions on Cybernetics
JF - IEEE Transactions on Cybernetics
IS - 7
M1 - 8674823
ER -