arXiv subjects

Jordan Jomsky

Publications and source records attributed to Jordan Jomsky.

3 recordsLinked to original sources

arXiv2026

Graph Neural Network Reveals the Cortical Morphology of Local Brain Aging in Normal Cognition and Alzheimer's Disease

Estimating brain age (BA) from T1-weighted magnetic resonance images (MRIs) provides a powerful framework for quantifying anatomical brain aging. Whereas global BA (GBA) summarizes overall brain health, local BA (LBA) provides cortically specific patterns of aging at the subject level. Although previous studies have examined anatomical contributors to GBA, to our knowledge, no framework has been established to estimate LBA using cortical morphology. To address this gap, we introduce a graph neural network (GNN) that uses morphometric features$\unicode{x2013}$cortical thickness, surface area, curvature, gray/white matter intensity ratio (GWR), sulcal depth$\unicode{x2013}$to estimate LBA across the cortical surface at high spatial resolution (mean inter-vertex distance = 1.37 mm). Trained on cortical surface meshes extracted from the MRIs of cognitively normal (CN) adults (N = 14,423), our model achieves lower mean absolute error (MAE) than the existing state-of-the-art while identifying more biologically plausible patterns of aging in Alzheimer's disease (AD) on the ADNI dataset. Association cortices emerge as primary sites of morphometric aging in CNs, whereas mild cognitive impairment is characterized by widespread aging that is pronounced in the parahippocampal gyrus. AD subjects demonstrate significant aging across the entire cortex, particularly within medial temporal regions and associated cortical networks. Feature ablation highlights curvature and GWR as preferentially sensitive to AD pathology. Regional LBA gaps are significantly associated with neuropsychological measures of AD-related cognitive impairment, linking cortical aging patterns to clinical outcomes. These results demonstrate that GNN-based modeling of cortical morphometry enables biologically interpretable mapping of local brain aging with greater interpretability than prior work.

q-bio.NC↗

arXiv2024

Enhancing brain age estimation with structural MRI and synthesized cerebral blood volume maps

BrainAGE is a promising imaging-derived biomarker of neurobiological ageing and disease risk, yet current approaches rely predominantly on T1-weighted structural MRI, overlooking functional vascular changes that may precede tissue damage and cognitive decline. DeepCBV maps, synthesized from non-contrast MRI, offer a scalable alternative to contrast-enhanced perfusion imaging by capturing vascular information relevant to early neurodegeneration. We developed a multimodal BrainAGE framework that combines predictions from two separate three-dimensional convolutional neural networks: one trained only on structural MRI scans and another trained only on DeepCBV maps. Each model was trained and validated on 2851 scans from 13 open-source datasets and was evaluated for concordance with MCI and AD. The combined model achieved the most accurate brain age gap for CN controls, with a mean absolute error of 3.95 years, outperforming models trained on MRI or DeepCBV alone. Saliency maps revealed complementary modality contributions: MRI emphasized white matter and cortical atrophy, while DeepCBV highlighted vascular-rich and periventricular regions implicated in hypoperfusion and early cerebrovascular dysfunction, consistent with known patterns of normal ageing. Next, we observed that BrainAGE increased stepwise across diagnostic strata (CN < MCI < AD) and correlated with cognitive impairment. DeepCBV-based BrainAGE showed a particularly strong separation between stable versus progressive MCI, suggesting sensitivity to prodromal vascular changes that precede overt atrophy. Integrating structural MRI with deep learning-derived vascular measures substantially enhances BrainAGE estimation and improves sensitivity to MCI and AD progression, supporting its potential role in risk stratification, early detection and monitoring of therapeutic response.

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arXiv2024

MedSegMamba: 3D CNN-Mamba Hybrid Architecture for Brain Segmentation

Widely used traditional pipelines for subcortical brain segmentation are often inefficient and slow, particularly when processing large datasets. Furthermore, deep learning models face challenges due to the high resolution of MRI images and the large number of anatomical classes involved. To address these limitations, we developed a 3D patch-based hybrid CNN-Mamba model that leverages Mamba's selective scan algorithm, thereby enhancing segmentation accuracy and efficiency for 3D inputs. This retrospective study utilized 1784 T1-weighted MRI scans from a diverse, multi-site dataset of healthy individuals. The dataset was divided into training, validation, and testing sets with a 1076/345/363 split. The scans were obtained from 1.5T and 3T MRI machines. Our model's performance was validated against several benchmarks, including other CNN-Mamba, CNN-Transformer, and pure CNN networks, using FreeSurfer-generated ground truths. We employed the Dice Similarity Coefficient (DSC), Volume Similarity (VS), and Average Symmetric Surface Distance (ASSD) as evaluation metrics. Statistical significance was determined using the Wilcoxon signed-rank test with a threshold of P < 0.05. The proposed model achieved the highest overall performance across all metrics (DSC 0.88383; VS 0.97076; ASSD 0.33604), significantly outperforming all non-Mamba-based models (P < 0.001). While the model did not show significant improvement in DSC or VS compared to another Mamba-based model (P-values of 0.114 and 0.425), it demonstrated a significant enhancement in ASSD (P < 0.001) with approximately 20% fewer parameters. In conclusion, our proposed hybrid CNN-Mamba architecture offers an efficient and accurate approach for 3D subcortical brain segmentation, demonstrating potential advantages over existing methods. Code is available at: https://github.com/aaroncao06/MedSegMamba.

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