{"title":"Analyzing Brain Tumor Connectomics using Graphs and Persistent Homology","authors":"Debanjali Bhattacharya, Ninad Aithal, Manish Jayswal, Neelam Sinha","doi":"arxiv-2407.17938","DOIUrl":null,"url":null,"abstract":"Recent advances in molecular and genetic research have identified a diverse\nrange of brain tumor sub-types, shedding light on differences in their\nmolecular mechanisms, heterogeneity, and origins. The present study performs\nwhole-brain connectome analysis using diffusionweighted images. To achieve\nthis, both graph theory and persistent homology - a prominent approach in\ntopological data analysis are employed in order to quantify changes in the\nstructural connectivity of the wholebrain connectome in subjects with brain\ntumors. Probabilistic tractography is used to map the number of streamlines\nconnecting 84 distinct brain regions, as delineated by the Desikan-Killiany\natlas from FreeSurfer. These streamline mappings form the connectome matrix, on\nwhich persistent homology based analysis and graph theoretical analysis are\nexecuted to evaluate the discriminatory power between tumor sub-types that\ninclude meningioma and glioma. A detailed statistical analysis is conducted on\npersistent homology-derived topological features and graphical features to\nidentify the brain regions where differences between study groups are\nstatistically significant (p < 0.05). For classification purpose, graph-based\nlocal features are utilized, achieving a highest accuracy of 88%. In\nclassifying tumor sub-types, an accuracy of 80% is attained. The findings\nobtained from this study underscore the potential of persistent homology and\ngraph theoretical analysis of the whole-brain connectome in detecting\nalterations in structural connectivity patterns specific to different types of\nbrain tumors.","PeriodicalId":501517,"journal":{"name":"arXiv - QuanBio - Neurons and Cognition","volume":"94 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Neurons and Cognition","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2407.17938","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Recent advances in molecular and genetic research have identified a diverse
range of brain tumor sub-types, shedding light on differences in their
molecular mechanisms, heterogeneity, and origins. The present study performs
whole-brain connectome analysis using diffusionweighted images. To achieve
this, both graph theory and persistent homology - a prominent approach in
topological data analysis are employed in order to quantify changes in the
structural connectivity of the wholebrain connectome in subjects with brain
tumors. Probabilistic tractography is used to map the number of streamlines
connecting 84 distinct brain regions, as delineated by the Desikan-Killiany
atlas from FreeSurfer. These streamline mappings form the connectome matrix, on
which persistent homology based analysis and graph theoretical analysis are
executed to evaluate the discriminatory power between tumor sub-types that
include meningioma and glioma. A detailed statistical analysis is conducted on
persistent homology-derived topological features and graphical features to
identify the brain regions where differences between study groups are
statistically significant (p < 0.05). For classification purpose, graph-based
local features are utilized, achieving a highest accuracy of 88%. In
classifying tumor sub-types, an accuracy of 80% is attained. The findings
obtained from this study underscore the potential of persistent homology and
graph theoretical analysis of the whole-brain connectome in detecting
alterations in structural connectivity patterns specific to different types of
brain tumors.