Predicting brain age with deep learning from raw imaging data results in a reliable and heritable biomarker.

Journal: NeuroImage
Published Date:

Abstract

Machine learning analysis of neuroimaging data can accurately predict chronological age in healthy people. Deviations from healthy brain ageing have been associated with cognitive impairment and disease. Here we sought to further establish the credentials of 'brain-predicted age' as a biomarker of individual differences in the brain ageing process, using a predictive modelling approach based on deep learning, and specifically convolutional neural networks (CNN), and applied to both pre-processed and raw T1-weighted MRI data. Firstly, we aimed to demonstrate the accuracy of CNN brain-predicted age using a large dataset of healthy adults (N = 2001). Next, we sought to establish the heritability of brain-predicted age using a sample of monozygotic and dizygotic female twins (N = 62). Thirdly, we examined the test-retest and multi-centre reliability of brain-predicted age using two samples (within-scanner N = 20; between-scanner N = 11). CNN brain-predicted ages were generated and compared to a Gaussian Process Regression (GPR) approach, on all datasets. Input data were grey matter (GM) or white matter (WM) volumetric maps generated by Statistical Parametric Mapping (SPM) or raw data. CNN accurately predicted chronological age using GM (correlation between brain-predicted age and chronological age r = 0.96, mean absolute error [MAE] = 4.16 years) and raw (r = 0.94, MAE = 4.65 years) data. This was comparable to GPR brain-predicted age using GM data (r = 0.95, MAE = 4.66 years). Brain-predicted age was a heritable phenotype for all models and input data (h ≥ 0.5). Brain-predicted age showed high test-retest reliability (intraclass correlation coefficient [ICC] = 0.90-0.99). Multi-centre reliability was more variable within high ICCs for GM (0.83-0.96) and poor-moderate levels for WM and raw data (0.51-0.77). Brain-predicted age represents an accurate, highly reliable and genetically-influenced phenotype, that has potential to be used as a biomarker of brain ageing. Moreover, age predictions can be accurately generated on raw T1-MRI data, substantially reducing computation time for novel data, bringing the process closer to giving real-time information on brain health in clinical settings.

Authors

  • James H Cole
    Computational, Clinical, and Cognitive Neuroimaging Laboratory, Department of Medicine, Imperial College London, London, United Kingdom.
  • Rudra P K Poudel
    Department of Biomedical Engineering, King's College London, London, UK.
  • Dimosthenis Tsagkrasoulis
    Department of Mathematics, Imperial College London, London, UK.
  • Matthan W A Caan
    Department of Radiology, Academic Medical Center, Amsterdam, The Netherlands.
  • Claire Steves
    Department of Twin Research & Genetic Epidemiology, King's College London, London, UK.
  • Tim D Spector
    Department of Twin Research & Genetic Epidemiology, King's College London, London, UK.
  • Giovanni Montana
    Department of Biomedical Engineering, King's College London, London SE1 7EH, United Kingdom.