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SA-AVAE: A sex-Aware adversarial variational autoencoder network for biological brain age estimation in IoMT-Enabled multimodal neuroimagesopen access

Authors
Rehman, Abd UrRehman, AzkaFarooq, Muhammad UmarLee, TaehyunKhan, Tariq M.Razzak, ImranGho, Sung-MinLee, AleumChae, Dong-KyuUsman, Muhammad
Issue Date
May-2026
Publisher
ELSEVIER
Keywords
Adversarial learning; Brain age; Cloud computing; Internet of medical things (iomt); Magnetic resonance imaging; Multimodal learning
Citation
INTERNET OF THINGS, v.37, pp 1 - 18
Pages
18
Indexed
SCIE
SCOPUS
Journal Title
INTERNET OF THINGS
Volume
37
Start Page
1
End Page
18
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/213820
DOI
10.1016/j.iot.2026.101893
ISSN
2543-1536
2542-6605
Abstract
Magnetic resonance imaging (MRI) of the brain, facilitated by IoMT-assisted telemedicine platforms, serves as a key biomarker for brain health determination through its structural and functional studies. Notably, combining structural MRI (sMRI) and functional MRI (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 distinct 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. Several 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.
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