TY - JOUR
T1 - Evaluating the reliability of neurocognitive biomarkers of neurodegenerative diseases across countries
T2 - A machine learning approach
AU - Bachli, M. Belen
AU - Sedeño, Lucas
AU - Ochab, Jeremi K.
AU - Piguet, Olivier
AU - Kumfor, Fiona
AU - Reyes, Pablo
AU - Torralva, Teresa
AU - Roca, María
AU - Cardona, Juan Felipe
AU - Campo, Cecilia Gonzalez
AU - Herrera, Eduar
AU - Slachevsky, Andrea
AU - Matallana, Diana
AU - Manes, Facundo
AU - García, Adolfo M.
AU - Ibáñez, Agustín
AU - Chialvo, Dante R.
N1 - Funding Information:
This work was supported by the Jagellonian University-UNSAM Cooperation Agreement , as well as the CEUNIM-INCYT-CEMSC 3 Collaboration Agreement. JKO was supported by the Grant DEC-2015/17/D/ST2/03492 of the National Science Centre (Poland) . DRC was supported in part by CONICET (Argentina) and Escuela de Ciencia y Tecnología, UNSAM . AI is supported by grants from CONICET; CONICYT/FONDECYT Regular ( 1170010 ); FONDAP 15150012 ; the Inter-American Development Bank (IDB) ; PICT , Grant/Award Number: 2017-1818 and 2017-1820 ; the INECO Foundation , by the National Institute On Aging of the National Institutes of Health under Award Number R01AG057234 , and by GBHI ALZ UK-20-639295 . PR and DM are supported by COLCIENCIAS grant 697-2014 . JF is supported by COLCIENCIAS grant 110674455314 . This work was also supported in part by funding to Forefront, a collaborative research group specialized in the study of frontotemporal dementia and motor neurone disease, from the National Health and Medical Research Council (NHMRC) of Australia program grant ( APP1037746 ) and the Australian Research Council (ARC) Centre of Excellence in Cognition and its Disorders Memory Program ( CE110001021 ). FK is supported by an NHMRC-ARC Dementia Research Development Fellowship ( APP1097026 ). OP is supported by an NHMRC Senior Research Fellowship ( APP1103258 ). AS is supported by FONDAP Program Grant 15150012
Publisher Copyright:
© 2019 The Authors
PY - 2020/3
Y1 - 2020/3
N2 - Accurate early diagnosis of neurodegenerative diseases represents a growing challenge for current clinical practice. Promisingly, current tools can be complemented by computational decision-support methods to objectively analyze multidimensional measures and increase diagnostic confidence. Yet, widespread application of these tools cannot be recommended unless they are proven to perform consistently and reproducibly across samples from different countries. We implemented machine-learning algorithms to evaluate the prediction power of neurocognitive biomarkers (behavioral and imaging measures) for classifying two neurodegenerative conditions –Alzheimer Disease (AD) and behavioral variant frontotemporal dementia (bvFTD)– across three different countries (>200 participants). We use machine-learning tools integrating multimodal measures such as cognitive scores (executive functions and cognitive screening) and brain atrophy volume (voxel based morphometry from fronto-temporo-insular regions in bvFTD, and temporo-parietal regions in AD) to identify the most relevant features in predicting the incidence of the diseases. In the Country-1 cohort, predictions of AD and bvFTD became maximally improved upon inclusion of cognitive screenings outcomes combined with atrophy levels. Multimodal training data from this cohort allowed predicting both AD and bvFTD in the other two novel datasets from other countries with high accuracy (>90%), demonstrating the robustness of the approach as well as the differential specificity and reliability of behavioral and neural markers for each condition. In sum, this is the first study, across centers and countries, to validate the predictive power of cognitive signatures combined with atrophy levels for contrastive neurodegenerative conditions, validating a benchmark for future assessments of reliability and reproducibility.
AB - Accurate early diagnosis of neurodegenerative diseases represents a growing challenge for current clinical practice. Promisingly, current tools can be complemented by computational decision-support methods to objectively analyze multidimensional measures and increase diagnostic confidence. Yet, widespread application of these tools cannot be recommended unless they are proven to perform consistently and reproducibly across samples from different countries. We implemented machine-learning algorithms to evaluate the prediction power of neurocognitive biomarkers (behavioral and imaging measures) for classifying two neurodegenerative conditions –Alzheimer Disease (AD) and behavioral variant frontotemporal dementia (bvFTD)– across three different countries (>200 participants). We use machine-learning tools integrating multimodal measures such as cognitive scores (executive functions and cognitive screening) and brain atrophy volume (voxel based morphometry from fronto-temporo-insular regions in bvFTD, and temporo-parietal regions in AD) to identify the most relevant features in predicting the incidence of the diseases. In the Country-1 cohort, predictions of AD and bvFTD became maximally improved upon inclusion of cognitive screenings outcomes combined with atrophy levels. Multimodal training data from this cohort allowed predicting both AD and bvFTD in the other two novel datasets from other countries with high accuracy (>90%), demonstrating the robustness of the approach as well as the differential specificity and reliability of behavioral and neural markers for each condition. In sum, this is the first study, across centers and countries, to validate the predictive power of cognitive signatures combined with atrophy levels for contrastive neurodegenerative conditions, validating a benchmark for future assessments of reliability and reproducibility.
KW - Alzheimer's disease
KW - Classification
KW - Executive functions
KW - Frontotemporal dementia
KW - Machine-learning
KW - Voxel-based morphometry
UR - http://www.scopus.com/inward/record.url?scp=85076710475&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2019.116456
DO - 10.1016/j.neuroimage.2019.116456
M3 - Article
C2 - 31841681
AN - SCOPUS:85076710475
SN - 1053-8119
VL - 208
JO - NeuroImage
JF - NeuroImage
M1 - 116456
ER -