4.7 Article

Deep transfer learning of structural magnetic resonance imaging fused with blood parameters improves brain age prediction

期刊

HUMAN BRAIN MAPPING
卷 43, 期 5, 页码 1640-1656

出版社

WILEY
DOI: 10.1002/hbm.25748

关键词

blood biochemical indicators; brain age; deep transfer learning; dementia-associated biomarkers; magnetic resonance imaging; multimodal data fusion

资金

  1. Guangdong Provincial Key ST Program [2018B030336001]
  2. National Natural Science Foundation of China [21877081]
  3. Nature Science Foundation of Shenzhen [JCYJ20200109114014533]
  4. Science, Technology and Innovation Commission of Shenzhen Municipality [JCYJ20200109110001818]
  5. Shenzhen-Hong Kong Institute of Brain Science-Shenzhen Fundamental Research Institutions [2021SHIBS0003]
  6. SZU Top Ranking Project, Shenzhen University [860/000002100108]
  7. Action Medical Research
  8. Medical Research Council (MRC)
  9. Engineering and Physical Sciences Research Council (EPSRC)
  10. European Research Council (ERC)
  11. National Institute of Biomedical Imaging and Bioengineering
  12. National Institute on Aging
  13. DOD ADNI [W81XWH-12-2-0012]
  14. National Institutes of Health [R01 EB009352, UL1 TR000448, R01 AG043434, P01 AG003991, P01 AG026276, P30 NS09857781, P50 AG00561, U01 AG024904]
  15. Alzheimer's Disease Neuroimaging Initiative

向作者/读者索取更多资源

Machine learning models combining brain structural MRI data and blood parameters show promising potential in accurately predicting brain age, with better performance in older age groups. The fusion model achieved a more accurate prediction of brain age by incorporating multiple indicators, showing significant improvements in evaluating brain health based on MRI and blood parameters.
Machine learning has been applied to neuroimaging data for estimating brain age and capturing early cognitive impairment in neurodegenerative diseases. Blood parameters like neurofilament light chain are associated with aging. In order to improve brain age predictive accuracy, we constructed a model based on both brain structural magnetic resonance imaging (sMRI) and blood parameters. Healthy subjects (n = 93; 37 males; aged 50-85 years) were recruited. A deep learning network was firstly pretrained on a large set of MRI scans (n = 1,481; 659 males; aged 50-85 years) downloaded from multiple open-source datasets, to provide weights on our recruited dataset. Evaluating the network on the recruited dataset resulted in mean absolute error (MAE) of 4.91 years and a high correlation (r = .67, p <.001) against chronological age. The sMRI data were then combined with five blood biochemical indicators including GLU, TG, TC, ApoA1 and ApoB, and 9 dementia-associated biomarkers including ApoE genotype, HCY, NFL, TREM2, A beta 40, A beta 42, T-tau, TIMP1, and VLDLR to construct a bilinear fusion model, which achieved a more accurate prediction of brain age (MAE, 3.96 years; r = .76, p <.001). Notably, the fusion model achieved better improvement in the group of older subjects (70-85 years). Extracted attention maps of the network showed that amygdala, pallidum, and olfactory were effective for age estimation. Mediation analysis further showed that brain structural features and blood parameters provided independent and significant impact. The constructed age prediction model may have promising potential in evaluation of brain health based on MRI and blood parameters.

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