Leveraging Persistent Homology for Differential Diagnosis of Mild Cognitive Impairment

Abstract

Mild cognitive impairment (MCI) is characterized by subtle changes in cognitive functions, often associated with disruptions in brain connectivity. The present study introduces a novel fine-grained analysis to examine topological alterations in neurodegeneration pertaining to six different brain networks of MCI subjects (Early/Late MCI). To achieve this, fMRI time series from two distinct populations are investigated: (i) the publicly accessible ADNI dataset and (ii) our in-house dataset. The study utilizes sliding window embedding to convert each fMRI time series into a sequence of 3-dimensional vectors, facilitating the assessment of changes in regional brain topology. Distinct persistence diagrams are computed for Betti descriptors of dimension-0, 1, and 2. Wasserstein distance metric is used to quantify differences in topological characteristics. We have examined both (i) ROI-specific inter-subject interactions and (ii) subject-specific inter-ROI interactions. Further, a new deep learning model is proposed for classification, achieving a maximum classification accuracy of 95% for the ADNI dataset and 85% for the in-house dataset. This methodology is further adapted for the differential diagnosis of MCI sub-types, resulting in a peak accuracy of 76.5%, 91.1% and 80% in classifying HC Vs. EMCI, HC Vs. LMCI and EMCI Vs. LMCI, respectively. We showed that the proposed approach surpasses current state-of-the-art techniques designed for classifying MCI and its sub-types using fMRI.