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...

Full description

Bibliographic Details
Main Authors: 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
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