Large-Scale Structural Covariance Networks Predict Age in Middle-to-Late Adulthood: A Novel Brain Aging Biomarker

Author:

Kuo Chen-Yuan1,Lee Pei-Lin2,Hung Sheng-Che3,Liu Li-Kuo45,Lee Wei-Ju46,Chung Chih-Ping78,Yang Albert C9,Tsai Shih-Jen9,Wang Pei-Ning7810,Chen Liang-Kung45,Chou Kun-Hsien210,Lin Ching-Po12410

Affiliation:

1. Department of Biomedical Imaging and Radiological Sciences, National Yang Ming University, Taipei 11221, Taiwan

2. Institute of Neuroscience, National Yang Ming University, Taipei 11221, Taiwan

3. Department of Radiology, University of North Carolina, Chapel Hill, NC 27514, USA

4. Aging and Health Research Center, National Yang Ming University, Taipei 11221, Taiwan

5. Center for Geriatrics and Gerontology, Taipei Veterans General Hospital, Taipei 11217, Taiwan

6. Department of Family Medicine, Yuanshan Branch, Taipei Veterans General Hospital, Yi-Lan 264, Taiwan

7. Department of Neurology, School of Medicine, National Yang Ming University, Taipei 11221, Taiwan

8. Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei 11217, Taiwan

9. Department of Psychiatry, Taipei Veterans General Hospital, Taipei 11217, Taiwan

10. Brain Research Center, National Yang Ming University, Taipei 11221, Taiwan

Abstract

Abstract The aging process is accompanied by changes in the brain’s cortex at many levels. There is growing interest in summarizing these complex brain-aging profiles into a single, quantitative index that could serve as a biomarker both for characterizing individual brain health and for identifying neurodegenerative and neuropsychiatric diseases. Using a large-scale structural covariance network (SCN)-based framework with machine learning algorithms, we demonstrate this framework’s ability to predict individual brain age in a large sample of middle-to-late age adults, and highlight its clinical specificity for several disease populations from a network perspective. A proposed estimator with 40 SCNs could predict individual brain age, balancing between model complexity and prediction accuracy. Notably, we found that the most significant SCN for predicting brain age included the caudate nucleus, putamen, hippocampus, amygdala, and cerebellar regions. Furthermore, our data indicate a larger brain age disparity in patients with schizophrenia and Alzheimer’s disease than in healthy controls, while this metric did not differ significantly in patients with major depressive disorder. These findings provide empirical evidence supporting the estimation of brain age from a brain network perspective, and demonstrate the clinical feasibility of evaluating neurological diseases hypothesized to be associated with accelerated brain aging.

Funder

Aging and Health Research Center

Center for Geriatrics and Gerontology of Taipei Veterans General Hospital of Taiwan

Ministry of Science and Technology

National Health Research Institutes

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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