TY - JOUR
T1 - Neuropsychiatric disease classification using functional connectomics- results of the connectomics in neuroimaging transfer learning challenge
AU - Schirmer, Markus D.
AU - Venkataraman, Archana
AU - Rekik, Islem
AU - Kim, Minjeong
AU - Mostofsky, Stewart H.
AU - Nebel, Mary Beth
AU - Rosch, Keri
AU - Seymour, Karen
AU - Crocetti, Deana
AU - Irzan, Hassna
AU - Hutel, Michael
AU - Ourselin, Sebastien
AU - Marlow, Neil
AU - Melbourne, Andrew
AU - Levchenko, Egor
AU - Zhou, Shuo
AU - Kunda, Mwiza
AU - Lu, Haiping
AU - Dvornek, Nicha C.
AU - Zhuang, Juntang
AU - Pinto, Gideon
AU - Samal, Sandip
AU - Zhang, Jennings
AU - Bernal-Rusiel, Jorge L.
AU - Pienaar, Rudolph
AU - Chung, Ai Wern
N1 - Funding Information:
The patient recruitment, data acquisition, and preprocessing was supported by the Autism Speaks Foundation (awards 1739 and 2384) and by the National Institutes of Health under the following awards: K02 NS44850 (PI Mostofsky), R01 MH078160-10 (PI Mostofsky), R01 MH085328-09 (PI Mostofsky), R01 MH106564-03 (PI Edden), K23 MH101322-05 (PI Rosch), K23 MH107734-05 (PI Seymour), R01 NS048527-08 (PI Mostofsky), R01 NS096207-05 (PI Mostofsky), R01MH085328-14 (PI Mostofsky), U54HD079123, UL RR025005, and P54 EB15909.
Funding Information:
A. Venkataraman was supported by the National Science Foundation Collaborative Research in Computational Neuroscience (CRCNS) award 1822575 and the National Science Foundation CAREER award 1845430.
Funding Information:
HSE: This work was supported by the Russian Academic Excellence Project ‘5-100’.
Funding Information:
MeInternational: This work was supported by the EPSRC-funded UCL Centre for Doctoral Training in Medical Imaging (EP/L016478/1); the National Institute for Health Research (NIHR); the Wellcome Trust (210182/Z/18/Z, 101957/Z/13/Z) and the Medical Research Council UK (Ref MR/J01107X/1).
Funding Information:
M. Kim was supported by UNC Greensboro New Faculty Award.
Funding Information:
ShefML: This work was supported by grants from the UK Engineering and Physical Sciences Research Council (EP/R014507/1).
Funding Information:
M. D. Schirmer was supported by the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 753896.
Funding Information:
I. Rekik is supported by the 2232 International Fellowship for Outstanding Researchers Program of TUBITAK (Project No:118C288) and the the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 101003403.
Funding Information:
A. W. Chung was supported by the American Heart Association and Children’s Heart Foundation Congenital Heart Defect Research Award, 19POST34380005.
Publisher Copyright:
© 2021
PY - 2021/5
Y1 - 2021/5
N2 - Large, open-source datasets, such as the Human Connectome Project and the Autism Brain Imaging Data Exchange, have spurred the development of new and increasingly powerful machine learning approaches for brain connectomics. However, one key question remains: are we capturing biologically relevant and generalizable information about the brain, or are we simply overfitting to the data? To answer this, we organized a scientific challenge, the Connectomics in NeuroImaging Transfer Learning Challenge (CNI-TLC), held in conjunction with MICCAI 2019. CNI-TLC included two classification tasks: (1) diagnosis of Attention-Deficit/Hyperactivity Disorder (ADHD) within a pre-adolescent cohort; and (2) transference of the ADHD model to a related cohort of Autism Spectrum Disorder (ASD) patients with an ADHD comorbidity. In total, 240 resting-state fMRI (rsfMRI) time series averaged according to three standard parcellation atlases, along with clinical diagnosis, were released for training and validation (120 neurotypical controls and 120 ADHD). We also provided Challenge participants with demographic information of age, sex, IQ, and handedness. The second set of 100 subjects (50 neurotypical controls, 25 ADHD, and 25 ASD with ADHD comorbidity) was used for testing. Classification methodologies were submitted in a standardized format as containerized Docker images through ChRIS, an open-source image analysis platform. Utilizing an inclusive approach, we ranked the methods based on 16 metrics: accuracy, area under the curve, F1-score, false discovery rate, false negative rate, false omission rate, false positive rate, geometric mean, informedness, markedness, Matthew's correlation coefficient, negative predictive value, optimized precision, precision, sensitivity, and specificity. The final rank was calculated using the rank product for each participant across all measures. Furthermore, we assessed the calibration curves of each methodology. Five participants submitted their method for evaluation, with one outperforming all other methods in both ADHD and ASD classification. However, further improvements are still needed to reach the clinical translation of functional connectomics. We have kept the CNI-TLC open as a publicly available resource for developing and validating new classification methodologies in the field of connectomics.
AB - Large, open-source datasets, such as the Human Connectome Project and the Autism Brain Imaging Data Exchange, have spurred the development of new and increasingly powerful machine learning approaches for brain connectomics. However, one key question remains: are we capturing biologically relevant and generalizable information about the brain, or are we simply overfitting to the data? To answer this, we organized a scientific challenge, the Connectomics in NeuroImaging Transfer Learning Challenge (CNI-TLC), held in conjunction with MICCAI 2019. CNI-TLC included two classification tasks: (1) diagnosis of Attention-Deficit/Hyperactivity Disorder (ADHD) within a pre-adolescent cohort; and (2) transference of the ADHD model to a related cohort of Autism Spectrum Disorder (ASD) patients with an ADHD comorbidity. In total, 240 resting-state fMRI (rsfMRI) time series averaged according to three standard parcellation atlases, along with clinical diagnosis, were released for training and validation (120 neurotypical controls and 120 ADHD). We also provided Challenge participants with demographic information of age, sex, IQ, and handedness. The second set of 100 subjects (50 neurotypical controls, 25 ADHD, and 25 ASD with ADHD comorbidity) was used for testing. Classification methodologies were submitted in a standardized format as containerized Docker images through ChRIS, an open-source image analysis platform. Utilizing an inclusive approach, we ranked the methods based on 16 metrics: accuracy, area under the curve, F1-score, false discovery rate, false negative rate, false omission rate, false positive rate, geometric mean, informedness, markedness, Matthew's correlation coefficient, negative predictive value, optimized precision, precision, sensitivity, and specificity. The final rank was calculated using the rank product for each participant across all measures. Furthermore, we assessed the calibration curves of each methodology. Five participants submitted their method for evaluation, with one outperforming all other methods in both ADHD and ASD classification. However, further improvements are still needed to reach the clinical translation of functional connectomics. We have kept the CNI-TLC open as a publicly available resource for developing and validating new classification methodologies in the field of connectomics.
KW - Functional connectomics
KW - Disease classification
KW - ADHD
KW - Challenge
UR - http://www.scopus.com/inward/record.url?scp=85102074399&partnerID=8YFLogxK
U2 - 10.1016/j.media.2021.101972
DO - 10.1016/j.media.2021.101972
M3 - Article
SN - 1361-8415
VL - 70
JO - Medical Image Analysis
JF - Medical Image Analysis
M1 - 101972
ER -