<p>As individuals age, cortical alterations in brain structure contribute to cognitive decline. However, the specific patterns of age-related changes and their impact on cognition remain poorly understood. This study assessed the effects of aging on individual gray matter similarity networks and compared them to anatomical and functional connectivity networks derived from diffusion-weighted imaging and resting-state fMRI, respectively. Our results showed that gray matter similarity networks outperformed anatomical and functional connectivity in predicting age and cognition, showing the earliest age-related changes across the adult lifespan. These networks also demonstrated greater robustness to individual differences in cognition, behavior, and sex. Notably, age-related changes in gray matter similarity were associated with the brain’s underlying cytoarchitecture, being strongest in brain regions from cortical layers II and III. These findings provide a new biological insight into the neural mechanisms of cognitive aging and highlight the potential of individual morphological similarity for capturing complex brain changes across the lifespan.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Similar minds age alike: an MRI similarity approach for predicting age-related cognitive decline

  • Blanca Zufiria-Gerbolés,
  • Jiawei Sun,
  • Jesús Pineda,
  • Giovanni Volpe,
  • Mite Mijalkov,
  • Joana B. Pereira

摘要

As individuals age, cortical alterations in brain structure contribute to cognitive decline. However, the specific patterns of age-related changes and their impact on cognition remain poorly understood. This study assessed the effects of aging on individual gray matter similarity networks and compared them to anatomical and functional connectivity networks derived from diffusion-weighted imaging and resting-state fMRI, respectively. Our results showed that gray matter similarity networks outperformed anatomical and functional connectivity in predicting age and cognition, showing the earliest age-related changes across the adult lifespan. These networks also demonstrated greater robustness to individual differences in cognition, behavior, and sex. Notably, age-related changes in gray matter similarity were associated with the brain’s underlying cytoarchitecture, being strongest in brain regions from cortical layers II and III. These findings provide a new biological insight into the neural mechanisms of cognitive aging and highlight the potential of individual morphological similarity for capturing complex brain changes across the lifespan.