Presenter Information

Location

https://www.kennesaw.edu/ccse/events/computing-showcase/sp26-cday-program.php

Document Type

Event

Start Date

22-4-2026 4:00 PM

Description

Deep graph learning has advanced Alzheimer’s disease (AD) classification from MRI, but most models remain correlational, confounding demographic and genetic factors with disease-specific features. We present Causal-GCN, an interventional graph convolutional framework that integrates do-calculus-based back-door adjustment to identify brain regions exerting stable causal influence on AD progression. Each subject’s MRI is represented as a structural connectome where nodes denote cortical and subcortical regions and edges encode anatomical connectivity. Confounders such as age, sex, and APOE4 genotype are summarized via principal components and included in the causal adjustment set. After training, interventions on individual regions are simulated by severing their incoming edges and altering node features to estimate average causal effects on disease probability. Applied to 484 subjects from the ADNI cohort, Causal-GCN achieves performance comparable to baseline GNNs while providing interpretable causal effect rankings that highlight posterior, cingulate, and insular hubs consistent with established AD neuropathology.

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Apr 22nd, 4:00 PM

GRM-132-159 Integrating Causal Inference with Graph Neural Networks for Alzheimer’s Disease Analysis

https://www.kennesaw.edu/ccse/events/computing-showcase/sp26-cday-program.php

Deep graph learning has advanced Alzheimer’s disease (AD) classification from MRI, but most models remain correlational, confounding demographic and genetic factors with disease-specific features. We present Causal-GCN, an interventional graph convolutional framework that integrates do-calculus-based back-door adjustment to identify brain regions exerting stable causal influence on AD progression. Each subject’s MRI is represented as a structural connectome where nodes denote cortical and subcortical regions and edges encode anatomical connectivity. Confounders such as age, sex, and APOE4 genotype are summarized via principal components and included in the causal adjustment set. After training, interventions on individual regions are simulated by severing their incoming edges and altering node features to estimate average causal effects on disease probability. Applied to 484 subjects from the ADNI cohort, Causal-GCN achieves performance comparable to baseline GNNs while providing interpretable causal effect rankings that highlight posterior, cingulate, and insular hubs consistent with established AD neuropathology.