🤖 AI Summary
This study addresses the challenge of leveraging persistent homology features of brain networks for group comparisons, which is hindered by individual heterogeneity and a lack of sensitivity to topological differences in lesion–symptom mapping. To overcome this, the authors propose a novel framework that transforms persistence diagrams into vectorized representations via heat diffusion, expressed as Fourier coefficients in the Laplace–Beltrami eigenfunction basis. They further introduce a transposed permutation test to enable statistically rigorous inference on higher-order topological structures across multiple groups. This approach uniquely integrates heat-diffusion-based persistence diagram representations with transposed permutation testing, and demonstrates robust performance in identifying topological cycles significantly associated with language impairment severity in post-stroke aphasia patients, even in the presence of topological noise and variability in cycle locations.
📝 Abstract
Persistent homology (PH) characterizes the shape of brain networks through persistence features. Group comparison of persistence features from brain networks can be challenging as they are inherently heterogeneous. A recent scale-space representation of persistence diagrams (PDs) through heat diffusion reparameterizes them using a finite number of Fourier coefficients with respect to the Laplace--Beltrami (LB) eigenfunction expansion of the domain, providing a powerful vectorized algebraic representation for group comparisons. In this study, we develop a transposition-based permutation test for comparing multiple groups of PDs using heat-diffusion estimates. We evaluate the empirical performance of the spectral transposition test in capturing within- and between-group similarity and dissimilarity under varying levels of topological noise and cycle location variability. In application, we propose a topological lesion symptom mapping (TLSM) method based on the proposed framework. The method is applied to resting-state functional brain networks of individuals with post-stroke aphasia to identify characteristic cycles associated with varying levels of speech-language impairment.