Unveiling Alzheimer's disease through brain age estimation using multi-kernel regression network and magnetic resonance imaging.

BACKGROUND AND

OBJECTIVE

Structural magnetic resonance imaging (MRI) studies have unveiled age-related anatomical changes across various brain regions. The disparity between actual age and estimated age, known as the Brain-Predicted Age Difference (Brain-PAD), serves as an indicator for predicting neurocognitive ailments or brain abnormalities resulting from diseases. This study aims to develop an accurate brain age prediction model that can assist in identifying potential neurocognitive impairments.

METHODS

The present study implemented a brain age prediction model using a ResNet-50 deep network and a multi-kernel extreme learning machine (MKELM) regression network, relying on MRI images. Kernel methods translate input information into higher-dimensional space by introducing nonlinearity and enabling the model to grasp complicated data patterns. A multi-kernel function combines the Gaussian and polynomial kernels and is incorporated into the brain age regression model. The model effectively utilizes the benefits of both kernel functions to estimate the ages accurately. MRI scans are segmented into gray matter (GM) and white matter (WM) maps preprocessed and extracted of significant features using the ResNet-50 deep network. Extracted features of the WM and GM datasets are fed into the MKELM regression model for brain age prediction.

RESULTS

The proposed age estimation framework achieved 3.06 years of mean absolute error (MAE) and 4.12 years of root mean square error (RMSE) on healthy controls (HC) WM scans, and on GM scans, 2.73 years of MAE and 3.65 years of RMSE values. To further validate the importance of Brain-PAD as a biomarker for identifying brain health conditions, an independent testing dataset of mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects age is predicted. The Brain-PAD values for AD subjects' GM images are significantly higher compared to those of HC and MCI subjects, indicating distinct brain health conditions. Furthermore, variations in GM and WM tissue were identified in AD subjects, revealing that the parahippocampus and corpus callosum were notably affected.

CONCLUSION

Our findings underscore the potential of Brain-PAD as a significant biomarker for assessing brain health, with implications for early detection of neurocognitive diseases. The developed framework effectively estimates brain age using MRI, contributing valuable insights into the relationship between brain structure and cognitive health.