Biological Brain Age Estimation using Sex-Aware Adversarial Variational Autoencoder with Multimodal Neuroimages

TL;DR

This paper introduces a novel sex-aware adversarial variational autoencoder framework that effectively fuses multimodal neuroimages to improve biological brain age estimation, capturing sex-specific aging patterns with high robustness.

Contribution

It proposes a new multimodal framework using a sex-aware adversarial variational autoencoder that disentangles shared and modality-specific features for accurate brain age estimation.

Findings

Outperforms existing methods in accuracy on the OpenBHB dataset

Demonstrates robustness across various age groups

Effectively captures sex-specific aging patterns

Abstract

Brain aging involves structural and functional changes and therefore serves as a key biomarker for brain health. Combining structural magnetic resonance imaging (sMRI) and functional magnetic resonance imaging (fMRI) has the potential to improve brain age estimation by leveraging complementary data. However, fMRI data, being noisier than sMRI, complicates multimodal fusion. Traditional fusion methods often introduce more noise than useful information, which can reduce accuracy compared to using sMRI alone. In this paper, we propose a novel multimodal framework for biological brain age estimation, utilizing a sex-aware adversarial variational autoencoder (SA-AVAE). Our framework integrates adversarial and variational learning to effectively disentangle the latent features from both modalities. Specifically, we decompose the latent space into modality-specific codes and shared codes to represent complementary and common information across modalities, respectively. To enhance the disentanglement, we introduce cross-reconstruction and shared-distinct distance ratio loss as regularization terms. Importantly, we incorporate sex information into the learned latent code, enabling the model to capture sex-specific aging patterns for brain age estimation via an integrated regressor module. We evaluate our model using the publicly available OpenBHB dataset, a comprehensive multi-site dataset for brain age estimation. The results from ablation studies and comparisons with state-of-the-art methods demonstrate that our framework outperforms existing approaches and shows significant robustness across various age groups, highlighting its potential for real-time clinical applications in the early detection of neurodegenerative diseases.