| Literature DB >> 32572452 |
Chen-Yuan Kuo1, Pei-Lin Lee2, Sheng-Che Hung3, Li-Kuo Liu4,5, Wei-Ju Lee4,6, Chih-Ping Chung7,8, Albert C Yang9, Shih-Jen Tsai9, Pei-Ning Wang7,8,10, Liang-Kung Chen4,5, Kun-Hsien Chou2,10, Ching-Po Lin1,2,4,10.
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.Entities:
Keywords: aging; brain age; machine learning; neurological diseases; structural covariance network (SCN)
Mesh:
Year: 2020 PMID: 32572452 DOI: 10.1093/cercor/bhaa161
Source DB: PubMed Journal: Cereb Cortex ISSN: 1047-3211 Impact factor: 5.357