Decoupling MCI-specific signatures from shared neurobiological substrates of cognitive aging via deep learning.
Authors
Affiliations (9)
Affiliations (9)
- State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, China.
- BABRI Centre, Beijing Normal University, Beijing, China.
- School of Systems Science, Beijing Normal University, Beijing, China.
- State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, China. [email protected].
- BABRI Centre, Beijing Normal University, Beijing, China. [email protected].
- State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, China. [email protected].
- State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, China. [email protected].
- BABRI Centre, Beijing Normal University, Beijing, China. [email protected].
- Innovation Institute of Integrated Traditional Chinese and Western Medicine, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, China. [email protected].
Abstract
The specific neuroanatomy of mild cognitive impairment (MCI) is obscured by its clinical heterogeneity and confounding effects from normative variation. This problem is compounded by the inability of conventional neuroimaging methods to disentangle these overlapping influences. Leveraging data from the Beijing Aging Brain Rejuvenation Initiative (BABRI, n = 918) and the Alzheimer's Disease Neuroimaging Initiative (ADNI, n = 1293), this study employed a conditional variational autoencoder (CVAE) to: (1) systematically distinguish between aging-related cognitive decline and MCI-specific cognitive impairments; (2) implicitly disentangle latent, unknown confounding effects to identify MCI-specific structural brain alterations; and (3) construct individualized scores for predicting the risk of conversion to Alzheimer's disease (AD). The CVAE effectively extracted MCI-specific latent features from T1 structural MRI, significantly correlated with episodic memory, attention, and executive function impairments. Reconstructions revealed characteristic deformation in regions including the middle and medial temporal lobes, frontal lobe, limbic system, and cerebellum. The robustness of this structural-cognitive impairment association model established in BABRI dataset was validated in the ADNI dataset. Moreover, predictive modeling using these features achieved superior AD-conversion prediction (AUC = 0.83) versus whole-brain atrophy (AUC = 0.74; p < 0.001) or CSF biomarkers (AUC = 0.77; p < 0.001).This work establishes a novel paradigm for isolating MCI-specific brain alterations from physiological aging.