<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Maldonado M</submitter><funding>BLRD VA</funding><funding>NIA NIH HHS</funding><funding>McNair Medical Institute</funding><funding>National Cancer Institute</funding><funding>MEDVAMC</funding><funding>NCI NIH HHS</funding><funding>VHA MERIT</funding><funding>National Institute on Aging</funding><funding>American Federation of Aging Research</funding><funding>CSRD VA</funding><pagination>497-504</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5989751</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Little is known about the brain mechanisms underlying cancer-associated weight loss (C-WL) in humans despite this condition negatively affecting their quality of life and survival. We tested the hypothesis that patients with C-WL have abnormal connectivity in homeostatic and hedonic brain pathways together with altered brain activity during food reward.&lt;h4>Methods&lt;/h4>In 12 patients with cancer and 12 healthy controls, resting-state functional connectivity (RSFC, resting brain activity observed through changes in blood flow in the brain which creates a blood oxygen level-dependent signal that can be measured using functional magnetic resonance imaging) was used to compare three brain regions hypothesized to play a role in C-WL: the hypothalamus (homeostatic), the nucleus</pubmed_abstract><journal>Journal of cachexia, sarcopenia and muscle</journal><pubmed_title>The habenula as a novel link between the homeostatic and hedonic pathways in cancer-associated weight loss: a pilot study.</pubmed_title><pmcid>PMC5989751</pmcid><funding_grant_id>T32AG000183</funding_grant_id><funding_grant_id>I01 CX000994</funding_grant_id><funding_grant_id>T32 AG000183</funding_grant_id><funding_grant_id>I01 CX000174</funding_grant_id><funding_grant_id>CX000174</funding_grant_id><funding_grant_id>I01 BX002807</funding_grant_id><funding_grant_id>I01BX002807</funding_grant_id><funding_grant_id>AG040583</funding_grant_id><funding_grant_id>3P30CA125123-08S2</funding_grant_id><funding_grant_id>P30 CA125123</funding_grant_id><funding_grant_id>CX000994</funding_grant_id><funding_grant_id>R03 AG040583</funding_grant_id><pubmed_authors>Viswanath H</pubmed_authors><pubmed_authors>Marcelli M</pubmed_authors><pubmed_authors>Molfese DL</pubmed_authors><pubmed_authors>Garcia JM</pubmed_authors><pubmed_authors>Salas R</pubmed_authors><pubmed_authors>Hayes TG</pubmed_authors><pubmed_authors>Mediwala S</pubmed_authors><pubmed_authors>Jones A</pubmed_authors><pubmed_authors>Curtis K</pubmed_authors><pubmed_authors>Maldonado M</pubmed_authors><pubmed_authors>Baldwin P</pubmed_authors></additional><is_claimable>false</is_claimable><name>The habenula as a novel link between the homeostatic and hedonic pathways in cancer-associated weight loss: a pilot study.</name><description>&lt;h4>Background&lt;/h4>Little is known about the brain mechanisms underlying cancer-associated weight loss (C-WL) in humans despite this condition negatively affecting their quality of life and survival. We tested the hypothesis that patients with C-WL have abnormal connectivity in homeostatic and hedonic brain pathways together with altered brain activity during food reward.&lt;h4>Methods&lt;/h4>In 12 patients with cancer and 12 healthy controls, resting-state functional connectivity (RSFC, resting brain activity observed through changes in blood flow in the brain which creates a blood oxygen level-dependent signal that can be measured using functional magnetic resonance imaging) was used to compare three brain regions hypothesized to play a role in C-WL: the hypothalamus (homeostatic), the nucleus</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jun</publication><modification>2025-04-05T13:14:43.461Z</modification><creation>2019-03-26T23:42:11Z</creation></dates><accession>S-EPMC5989751</accession><cross_references><pubmed>29575771</pubmed><doi>10.1002/jcsm.12286</doi></cross_references></HashMap>