Anatomically interpretable deep learning of brain age captures domain-specific cognitive impairment

神经认知 痴呆 认知 心理学 神经影像学 神经解剖学 队列 衰老的大脑 基于体素的形态计量学 神经科学 听力学 疾病 磁共振成像 医学 白质 病理 放射科
作者
Chenzhong Yin,Phoebe Imms,Mingxi Cheng,Anar Amgalan,Nahian F. Chowdhury,Roy J Massett,Nikhil N. Chaudhari,Xinghe Chen,Paul M. Thompson,Paul Bogdan,Andrei Irimia,Michael W. Weiner,Paul Aisen,Ronald Petersen,Michael W. Weiner,Paul Aisen,Ronald Petersen,Clifford R. Jack,William J. Jagust,John Q. Trojanowki
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [National Academy of Sciences]
卷期号:120 (2) 被引量:71
标识
DOI:10.1073/pnas.2214634120
摘要

The gap between chronological age (CA) and biological brain age, as estimated from magnetic resonance images (MRIs), reflects how individual patterns of neuroanatomic aging deviate from their typical trajectories. MRI-derived brain age (BA) estimates are often obtained using deep learning models that may perform relatively poorly on new data or that lack neuroanatomic interpretability. This study introduces a convolutional neural network (CNN) to estimate BA after training on the MRIs of 4,681 cognitively normal (CN) participants and testing on 1,170 CN participants from an independent sample. BA estimation errors are notably lower than those of previous studies. At both individual and cohort levels, the CNN provides detailed anatomic maps of brain aging patterns that reveal sex dimorphisms and neurocognitive trajectories in adults with mild cognitive impairment (MCI, N = 351) and Alzheimer’s disease (AD, N = 359). In individuals with MCI (54% of whom were diagnosed with dementia within 10.9 y from MRI acquisition), BA is significantly better than CA in capturing dementia symptom severity, functional disability, and executive function. Profiles of sex dimorphism and lateralization in brain aging also map onto patterns of neuroanatomic change that reflect cognitive decline. Significant associations between BA and neurocognitive measures suggest that the proposed framework can map, systematically, the relationship between aging-related neuroanatomy changes in CN individuals and in participants with MCI or AD. Early identification of such neuroanatomy changes can help to screen individuals according to their AD risk.

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