4.7 Article

Evaluating the reliability of neurocognitive biomarkers of neurodegenerative diseases across countries: A machine learning approach

期刊

NEUROIMAGE
卷 208, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2019.116456

关键词

Alzheimer's disease; Frontotemporal dementia; Machine-learning; Executive functions; Voxel-based morphometry; Classification

资金

  1. Jagellonian University-UNSAM Cooperation Agreement
  2. CEUNIM-INCYT-CEMSC3 Collaboration Agreement
  3. National Science Centre (Poland) [DEC-2015/17/D/ST2/03492]
  4. CONICET (Argentina)
  5. Escuela de Ciencia y Tecnologia, UNSAM
  6. CONICET
  7. CONICYT/FONDECYT Regular [1170010]
  8. FONDAP [15150012]
  9. InterAmerican Development Bank (IDB)
  10. PICT [20171818, 2017-1820]
  11. INECO Foundation
  12. National Institute On Aging of the National Institutes of Health [R01AG057234]
  13. GBHI ALZ [UK-20-639295]
  14. COLCIENCIAS grant [697-2014, 110674455314]
  15. National Health and Medical Research Council (NHMRC) of Australia [APP1037746]
  16. Australian Research Council (ARC) Centre of Excellence in Cognition and its Disorders Memory Program [CE110001021]
  17. NHMRC-ARC Dementia Research Development Fellowship [APP1097026]
  18. NHMRC Senior Research Fellowship [APP1103258]
  19. FONDAP Program [15150012]

向作者/读者索取更多资源

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.

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