The habenula as a novel link between the homeostatic and hedonic pathways in cancer‐associated weight loss: a pilot study
Abstract Background 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 hedo...
Main Authors: | , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2018-06-01
|
Series: | Journal of Cachexia, Sarcopenia and Muscle |
Subjects: | |
Online Access: | https://doi.org/10.1002/jcsm.12286 |
id |
doaj-5ee79b936d7a4beaa655afeeff0896e8 |
---|---|
record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Maria Maldonado David L. Molfese Humsini Viswanath Kaylah Curtis Ashley Jones Teresa G. Hayes Marco Marcelli Sanjay Mediwala Philip Baldwin Jose M. Garcia Ramiro Salas |
spellingShingle |
Maria Maldonado David L. Molfese Humsini Viswanath Kaylah Curtis Ashley Jones Teresa G. Hayes Marco Marcelli Sanjay Mediwala Philip Baldwin Jose M. Garcia Ramiro Salas The habenula as a novel link between the homeostatic and hedonic pathways in cancer‐associated weight loss: a pilot study Journal of Cachexia, Sarcopenia and Muscle Cancer cachexia Cancer anorexia Resting‐state functional connectivity Habenula Hypothalamus Nucleus accumbens |
author_facet |
Maria Maldonado David L. Molfese Humsini Viswanath Kaylah Curtis Ashley Jones Teresa G. Hayes Marco Marcelli Sanjay Mediwala Philip Baldwin Jose M. Garcia Ramiro Salas |
author_sort |
Maria Maldonado |
title |
The habenula as a novel link between the homeostatic and hedonic pathways in cancer‐associated weight loss: a pilot study |
title_short |
The habenula as a novel link between the homeostatic and hedonic pathways in cancer‐associated weight loss: a pilot study |
title_full |
The habenula as a novel link between the homeostatic and hedonic pathways in cancer‐associated weight loss: a pilot study |
title_fullStr |
The habenula as a novel link between the homeostatic and hedonic pathways in cancer‐associated weight loss: a pilot study |
title_full_unstemmed |
The habenula as a novel link between the homeostatic and hedonic pathways in cancer‐associated weight loss: a pilot study |
title_sort |
habenula as a novel link between the homeostatic and hedonic pathways in cancer‐associated weight loss: a pilot study |
publisher |
Wiley |
series |
Journal of Cachexia, Sarcopenia and Muscle |
issn |
2190-5991 2190-6009 |
publishDate |
2018-06-01 |
description |
Abstract Background 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. Methods 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 accumbens (hedonic), and the habenula (an important regulator of reward). In addition, the brain reward response to juice was studied. Participants included 12 patients with histological diagnosis of incurable cancer (solid tumours), a European Cooperative Oncology Group performance status of 0–2, and a ≥5% involuntary body weight loss from pre‐illness over the previous 6 months and 12 non‐cancer controls matched for age, sex, and race. RSFC between the hypothalamus, nucleus accumbens, and habenula and brain striatum activity as measured by functional MRI during juice reward delivery events were the main outcome measures. Results After adjusting for BMI and compared with matched controls, patients with C‐WL were found to have reduced RSFC between the habenula and hypothalamus (P = 0.04) and between the habenula and nucleus accumbens (P = 0.014). Patients with C‐WL also had reduced juice reward responses in the striatum compared with controls. Conclusions In patients with C‐WL, reduced connectivity between both homeostatic and hedonic brain regions and the habenula and reduced juice reward were observed. Further research is needed to establish the relevance of the habenula and striatum in C‐WL. |
topic |
Cancer cachexia Cancer anorexia Resting‐state functional connectivity Habenula Hypothalamus Nucleus accumbens |
url |
https://doi.org/10.1002/jcsm.12286 |
work_keys_str_mv |
AT mariamaldonado thehabenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT davidlmolfese thehabenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT humsiniviswanath thehabenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT kaylahcurtis thehabenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT ashleyjones thehabenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT teresaghayes thehabenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT marcomarcelli thehabenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT sanjaymediwala thehabenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT philipbaldwin thehabenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT josemgarcia thehabenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT ramirosalas thehabenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT mariamaldonado habenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT davidlmolfese habenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT humsiniviswanath habenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT kaylahcurtis habenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT ashleyjones habenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT teresaghayes habenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT marcomarcelli habenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT sanjaymediwala habenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT philipbaldwin habenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT josemgarcia habenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy AT ramirosalas habenulaasanovellinkbetweenthehomeostaticandhedonicpathwaysincancerassociatedweightlossapilotstudy |
_version_ |
1725447020489998336 |
spelling |
doaj-5ee79b936d7a4beaa655afeeff0896e82020-11-24T23:59:38ZengWileyJournal of Cachexia, Sarcopenia and Muscle2190-59912190-60092018-06-019349750410.1002/jcsm.12286The habenula as a novel link between the homeostatic and hedonic pathways in cancer‐associated weight loss: a pilot studyMaria Maldonado0David L. Molfese1Humsini Viswanath2Kaylah Curtis3Ashley Jones4Teresa G. Hayes5Marco Marcelli6Sanjay Mediwala7Philip Baldwin8Jose M. Garcia9Ramiro Salas10Division of Endocrinology, Diabetes and Metabolism, MCL, Center for Translational Research on Inflammatory Diseases, Dan L. Duncan Cancer Center, Michael E. DeBakey Veterans Affairs Medical Center, Dept. of Medicine Baylor College of Medicine Houston TX 77030 USAMenninger Department of Psychiatry and Behavioral Sciences Baylor College of Medicine Houston TX 77030 USAMenninger Department of Psychiatry and Behavioral Sciences Baylor College of Medicine Houston TX 77030 USAMenninger Department of Psychiatry and Behavioral Sciences Baylor College of Medicine Houston TX 77030 USADivision of Endocrinology, Diabetes and Metabolism, MCL, Center for Translational Research on Inflammatory Diseases, Dan L. Duncan Cancer Center, Michael E. DeBakey Veterans Affairs Medical Center, Dept. of Medicine Baylor College of Medicine Houston TX 77030 USADivision of Oncology and Hematology, MCL, Dan L. Duncan Cancer Center, Michael E. DeBakey Veterans Affairs Medical Center, Dept. of Medicine Baylor College of Medicine Houston TX 77030 USADivision of Endocrinology, Diabetes and Metabolism, MCL, Center for Translational Research on Inflammatory Diseases, Dan L. Duncan Cancer Center, Michael E. DeBakey Veterans Affairs Medical Center, Dept. of Medicine Baylor College of Medicine Houston TX 77030 USADivision of Endocrinology, Diabetes and Metabolism, MCL, Center for Translational Research on Inflammatory Diseases, Dan L. Duncan Cancer Center, Michael E. DeBakey Veterans Affairs Medical Center, Dept. of Medicine Baylor College of Medicine Houston TX 77030 USAMenninger Department of Psychiatry and Behavioral Sciences Baylor College of Medicine Houston TX 77030 USADivision of Endocrinology, Diabetes and Metabolism, MCL, Center for Translational Research on Inflammatory Diseases, Dan L. Duncan Cancer Center, Michael E. DeBakey Veterans Affairs Medical Center, Dept. of Medicine Baylor College of Medicine Houston TX 77030 USAMenninger Department of Psychiatry and Behavioral Sciences Baylor College of Medicine Houston TX 77030 USAAbstract Background 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. Methods 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 accumbens (hedonic), and the habenula (an important regulator of reward). In addition, the brain reward response to juice was studied. Participants included 12 patients with histological diagnosis of incurable cancer (solid tumours), a European Cooperative Oncology Group performance status of 0–2, and a ≥5% involuntary body weight loss from pre‐illness over the previous 6 months and 12 non‐cancer controls matched for age, sex, and race. RSFC between the hypothalamus, nucleus accumbens, and habenula and brain striatum activity as measured by functional MRI during juice reward delivery events were the main outcome measures. Results After adjusting for BMI and compared with matched controls, patients with C‐WL were found to have reduced RSFC between the habenula and hypothalamus (P = 0.04) and between the habenula and nucleus accumbens (P = 0.014). Patients with C‐WL also had reduced juice reward responses in the striatum compared with controls. Conclusions In patients with C‐WL, reduced connectivity between both homeostatic and hedonic brain regions and the habenula and reduced juice reward were observed. Further research is needed to establish the relevance of the habenula and striatum in C‐WL.https://doi.org/10.1002/jcsm.12286Cancer cachexiaCancer anorexiaResting‐state functional connectivityHabenulaHypothalamusNucleus accumbens |