<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Pan Y</submitter><funding>NIBIB NIH HHS</funding><funding>NIDA NIH HHS</funding><funding>NIA NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NIH HHS</funding><pubmed_abstract>The functional connectome changes with aging. We systematically evaluated aging related alterations in the functional connectome using a whole-brain connectome network analysis in 39,675 participants in UK Biobank project. We used adaptive dense network discovery tools to identify networks directly associated with aging from resting-state fMRI data. We replicated our findings in 499 participants from the Lifespan Human Connectome Project in Aging study. The results consistently revealed two motor-related subnetworks (both permutation test p-values &lt;0.001) that showed a decline in resting-state functional connectivity (rsFC) with increasing age. The first network primarily comprises sensorimotor and dorsal/ventral attention regions from precentral gyrus, postcentral gyrus, superior temporal gyrus, and insular gyrus, while the second network is exclusively composed of basal ganglia regions, namely the caudate, putamen, and globus pallidus. Path analysis indicates that white matter fractional anisotropy mediates 19.6% (p&lt;0.001, 95% CI [7.6% 36.0%]) and 11.5% (p&lt;0.001, 95% CI [6.3% 17.0%]) of the age-related decrease in both networks, respectively. The total volume of white matter hyperintensity mediates 32.1% (p&lt;0.001, 95% CI [16.8% 53.0%]) of the aging-related effect on rsFC in the first subnetwork.</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2024.05.17.594743</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11118564</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Brain-wide functional connectome analysis of 40,000 individuals reveals brain networks that show aging effects in older adults.</pubmed_title><pmcid>PMC11118564</pmcid><funding_grant_id>U01 MH108148</funding_grant_id><funding_grant_id>S10 OD023696</funding_grant_id><funding_grant_id>R01 NS114628</funding_grant_id><funding_grant_id>RF1 NS114628</funding_grant_id><funding_grant_id>R01 MH116948</funding_grant_id><funding_grant_id>DP1 DA048968</funding_grant_id><funding_grant_id>RF1 MH123163</funding_grant_id><funding_grant_id>R01 EB015611</funding_grant_id><funding_grant_id>K01 DA059603</funding_grant_id><funding_grant_id>P30 AG028747</funding_grant_id><pubmed_authors>Pan Y</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Lee H</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Ma T</pubmed_authors><pubmed_authors>Kochunov P</pubmed_authors><pubmed_authors>Shardell M</pubmed_authors><pubmed_authors>Ye Z</pubmed_authors><pubmed_authors>Nichols T</pubmed_authors><pubmed_authors>Hong LE</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Bi C</pubmed_authors><pubmed_authors>McCoy RG</pubmed_authors><pubmed_authors>Lu T</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Smith JC</pubmed_authors><pubmed_authors>Gao S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Brain-wide functional connectome analysis of 40,000 individuals reveals brain networks that show aging effects in older adults.</name><description>The functional connectome changes with aging. We systematically evaluated aging related alterations in the functional connectome using a whole-brain connectome network analysis in 39,675 participants in UK Biobank project. We used adaptive dense network discovery tools to identify networks directly associated with aging from resting-state fMRI data. We replicated our findings in 499 participants from the Lifespan Human Connectome Project in Aging study. The results consistently revealed two motor-related subnetworks (both permutation test p-values &lt;0.001) that showed a decline in resting-state functional connectivity (rsFC) with increasing age. The first network primarily comprises sensorimotor and dorsal/ventral attention regions from precentral gyrus, postcentral gyrus, superior temporal gyrus, and insular gyrus, while the second network is exclusively composed of basal ganglia regions, namely the caudate, putamen, and globus pallidus. Path analysis indicates that white matter fractional anisotropy mediates 19.6% (p&lt;0.001, 95% CI [7.6% 36.0%]) and 11.5% (p&lt;0.001, 95% CI [6.3% 17.0%]) of the age-related decrease in both networks, respectively. The total volume of white matter hyperintensity mediates 32.1% (p&lt;0.001, 95% CI [16.8% 53.0%]) of the aging-related effect on rsFC in the first subnetwork.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-05-29T03:11:24.026Z</modification><creation>2026-05-29T03:06:14.921Z</creation></dates><accession>S-EPMC11118564</accession><cross_references><pubmed>38798606</pubmed><doi>10.1101/2024.05.17.594743</doi></cross_references></HashMap>