Controllable Surface Diffusion Generative Model for Neurodevelopmental Trajectories

📅 2025-07-21
📈 Citations: 0
Influential: 0
📄 PDF
🤖 AI Summary
Preterm birth significantly disrupts cortical neurodevelopmental trajectories, yet individual outcomes vary widely—necessitating interpretable, subject-specific developmental modeling to identify early biomarkers. Existing generative models fail to preserve subject-specific cortical folding topology and regional morphometry. To address this, we propose a controllable graph diffusion generative framework grounded in dHCP infant cortical surface data, integrating graph-structured anatomical priors with age-conditioned control mechanisms to accurately simulate individualized cortical maturation trajectories. The model faithfully preserves topological fidelity while recapitulating region-specific developmental changes. Validation using an independent age-regression network demonstrates strong biological plausibility: predicted ages from generated surfaces achieve a mean absolute error of 0.85 ± 0.62 years. This work advances personalized neurodevelopmental modeling and holds promise for early clinical biomarker discovery.

Technology Category

Application Category

📝 Abstract
Preterm birth disrupts the typical trajectory of cortical neurodevelopment, increasing the risk of cognitive and behavioral difficulties. However, outcomes vary widely, posing a significant challenge for early prediction. To address this, individualized simulation offers a promising solution by modeling subject-specific neurodevelopmental trajectories, enabling the identification of subtle deviations from normative patterns that might act as biomarkers of risk. While generative models have shown potential for simulating neurodevelopment, prior approaches often struggle to preserve subject-specific cortical folding patterns or to reproduce region-specific morphological variations. In this paper, we present a novel graph-diffusion network that supports controllable simulation of cortical maturation. Using cortical surface data from the developing Human Connectome Project (dHCP), we demonstrate that the model maintains subject-specific cortical morphology while modeling cortical maturation sufficiently well to fool an independently trained age regression network, achieving a prediction accuracy of $0.85 pm 0.62$.
Problem

Research questions and friction points this paper is trying to address.

Predicting preterm infants' neurodevelopmental risks early
Modeling subject-specific cortical maturation trajectories accurately
Preserving individual cortical folding patterns in simulations
Innovation

Methods, ideas, or system contributions that make the work stand out.

Graph-diffusion network for cortical maturation simulation
Preserves subject-specific cortical folding patterns
Models region-specific morphological variations accurately
🔎 Similar Papers
No similar papers found.
Z
Zhenshan Xie
Research Department of Biomedical Computing, School of Biomedical Engineering & Imaging Sciences, King’s College London
L
Levente Baljer
Research Department of Biomedical Computing, School of Biomedical Engineering & Imaging Sciences, King’s College London
M
M. J. Cardoso
Research Department of Biomedical Computing, School of Biomedical Engineering & Imaging Sciences, King’s College London
Emma C. Robinson
Emma C. Robinson
Kings College London
Medical Image Computingconnectomicsregistration