<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Razban RM</submitter><funding>NIDA NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>Foundation for the National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><pagination>e0331085</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12425331</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(9)</volume><pubmed_abstract>Structure determines function. However, this universal theme in biology has been surprisingly difficult to observe in human brain neuroimaging data. Here, we link structure to function by hypothesizing that brain signals propagate as a Markovian process on an underlying structure. We focus on a metric called commute time: the average number of steps for a random walker to go from region A to B and then back to A. Commute times based on white matter tracts from diffusion MRI exhibit an average ± standard deviation Spearman correlation of -0.26 ± 0.08 with functional MRI connectivity data across 434 UK Biobank individuals and -0.24 ± 0.06 across 400 HCP Young Adult brain scans. The correlation increases to -0.36 ± 0.14 and to -0.32 ± 0.12 when the principal contributions of both commute time and functional connectivity are compared for both datasets. The correlations are stronger by 33% compared to broadly used communication measures such as search information and communicability. The difference further widens to a factor of 5 when commute times are correlated to the principal mode of functional connectivity from its eigenvalue decomposition. Overall, the study points to the utility of commute time to account for the role of polysynaptic (indirect) connectivity underlying brain function by assuming that signals randomly traverse along the underlying brain structure.</pubmed_abstract><journal>PloS one</journal><pubmed_title>The role of structural connectivity on brain function through a Markov model of signal transmission.</pubmed_title><pmcid>PMC12425331</pmcid><funding_grant_id>R01 GM139297</funding_grant_id><funding_grant_id>U54 MH091657</funding_grant_id><funding_grant_id>R01 DK116780</funding_grant_id><funding_grant_id>R01 DA062680</funding_grant_id><pubmed_authors>Bahar I</pubmed_authors><pubmed_authors>Razban RM</pubmed_authors><pubmed_authors>Banerjee A</pubmed_authors><pubmed_authors>Mujica-Parodi LR</pubmed_authors></additional><is_claimable>false</is_claimable><name>The role of structural connectivity on brain function through a Markov model of signal transmission.</name><description>Structure determines function. However, this universal theme in biology has been surprisingly difficult to observe in human brain neuroimaging data. Here, we link structure to function by hypothesizing that brain signals propagate as a Markovian process on an underlying structure. We focus on a metric called commute time: the average number of steps for a random walker to go from region A to B and then back to A. Commute times based on white matter tracts from diffusion MRI exhibit an average ± standard deviation Spearman correlation of -0.26 ± 0.08 with functional MRI connectivity data across 434 UK Biobank individuals and -0.24 ± 0.06 across 400 HCP Young Adult brain scans. The correlation increases to -0.36 ± 0.14 and to -0.32 ± 0.12 when the principal contributions of both commute time and functional connectivity are compared for both datasets. The correlations are stronger by 33% compared to broadly used communication measures such as search information and communicability. The difference further widens to a factor of 5 when commute times are correlated to the principal mode of functional connectivity from its eigenvalue decomposition. Overall, the study points to the utility of commute time to account for the role of polysynaptic (indirect) connectivity underlying brain function by assuming that signals randomly traverse along the underlying brain structure.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-06-03T02:28:06.725Z</modification><creation>2026-04-23T03:10:38.622Z</creation></dates><accession>S-EPMC12425331</accession><cross_references><pubmed>40934275</pubmed><doi>10.1371/journal.pone.0331085</doi></cross_references></HashMap>