4.7 Article

Multi-region analysis of longitudinal FDG-PET for the classification of Alzheimer's disease

期刊

NEUROIMAGE
卷 60, 期 1, 页码 221-229

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2011.12.071

关键词

Alzheimer's disease; Mild cognitive impairment; Classification; Longitudinal analysis; [18F]fluorodeoxyglucose positron emission tomography; Image segmentation

资金

  1. European Commission
  2. Engineering and Physical Sciences Research Council
  3. Dunhill Medical Trust
  4. Alzheimer's Disease Neuroimaging Initiative (ADNI) (National Institutes of Health) [U01 AG024904]
  5. National Institute on Aging
  6. National Institute of Biomedical Imaging and Bioengineering
  7. NIH [P30 AG010129, K01 AG030514]
  8. Dana Foundation
  9. Medical Research Council [G108/585] Funding Source: researchfish
  10. MRC [G108/585] Funding Source: UKRI

向作者/读者索取更多资源

Imaging biomarkers for Alzheimer's disease are desirable for improved diagnosis and monitoring, as well as drug discovery. Automated image-based classification of individual patients could provide valuable diagnostic support for clinicians, when considered alongside cognitive assessment scores. We investigate the value of combining cross-sectional and longitudinal multi-region FDG-PET information for classification, using clinical and imaging data from the Alzheimer's Disease Neuroimaging Initiative. Whole-brain segmentations into 83 anatomically defined regions were automatically generated for baseline and 12-month FDG-PET images. Regional signal intensities were extracted at each timepoint, as well as changes in signal intensity over the follow-up period. Features were provided to a support vector machine classifier. By combining 12-month signal intensities and changes over 12 months, we achieve significantly increased classification performance compared with using any of the three feature sets independently. Based on this combined feature set, we report classification accuracies of 88% between patients with Alzheimer's disease and elderly healthy controls, and 65% between patients with stable mild cognitive impairment and those who subsequently progressed to Alzheimer's disease. We demonstrate that information extracted from serial FDG-PET through regional analysis can be used to achieve state-of-the-art classification of diagnostic groups in a realistic multi-centre setting. This finding may be usefully applied in the diagnosis of Alzheimer's disease, predicting disease course in individuals with mild cognitive impairment, and in the selection of participants for clinical trials. (C) 2012 Elsevier Inc. All tights reserved.

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