Evidence map›Paper›PMID 29899546›Full record

ArticleMolecular psychiatry2020

Appetite changes reveal depression subgroups with distinct endocrine, metabolic, and immune states.

W Kyle Simmons, Kaiping Burrows, Jason A Avery, Kara L Kerr, Ashlee Taylor, Jerzy Bodurka, William Potter, T Kent Teague, Wayne C Drevets

Abstract read
In one paragraph

Article in Molecular psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed, 5 pooled it
17.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

85 citing papers in PubMed, 5 syntheses or guidelines pooled it, 181 citations in OpenAlex.

  1. Pooled it
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  6. Trial
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  8. Article
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  12. Article
  13. Symptom-specific genetics reveal heterogeneity within major depressive disorder.medRxiv : the preprint server for health sciences · 2026
    Article
  14. Article
  15. Obesity and Depression.Advances in experimental medicine and biology · 2026
    Review
  16. Review
  17. Article
  18. Article
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  20. Review

25 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 6 institutions in 1 country.

W Kyle SimmonsLaureate Institute for Brain Research, Tulsa, OK, USA. wsimmon1@its.jnj.com.
Kaiping BurrowsLaureate Institute for Brain Research, Tulsa, OK, USA.
Kara L KerrDepartment of Psychology, The University of Tulsa, Tulsa, OK, USA.
Ashlee TaylorIntegrative Immunology Center, The Oklahoma State University Center for Health Sciences, Tulsa, OK, USA.
Jerzy BodurkaStephenson School of Biomedical Engineering, The University of Oklahoma, Norman, OK, USA.
William PotterDepartment of Chemistry and Biochemistry, The University of Tulsa, Tulsa, OK, USA.
T Kent TeagueDepartments of Surgery and Psychiatry, School of Community Medicine, The University of Oklahoma, Tulsa, OK, USA.
Wayne C DrevetsJanssen Research and Development, LLC., Titusville, NJ, USA.
Oklahoma State University Center for Health Sciences · USUniversity of Tulsa · USJanssen (United States) · USLaureate Institute for Brain Research · USTulsa Community College · USUniversity of Oklahoma · US

Funding

The Center for Neuroscience-based Mental Health Assessment and Prediction (NEUROMAP)P20GM121312 · NIGMS · LAUREATE INSTITUTE FOR BRAIN RESEARCH · PI Maëlle Camille Marie Gueguen · 2017 to 2026
$23.7M
The Neural Bases of Pathological Food Perception and Choice in Major DepressionK01MH096175 · NIMH · LAUREATE INSTITUTE FOR BRAIN RESEARCH · PI SIMMONS, WILLIAM KYLE · 2012 to 2016
$904k
NIGMS NIH HHS P20 GM121312NIMH NIH HHS K01 MH096175
6 · The paper itself

Abstract

There exists little human neuroscience research to explain why some individuals lose their appetite when they become depressed, while others eat more. Answering this question may reveal much about the various pathophysiologies underlying depression. The present study combined neuroimaging, salivary cortisol, and blood markers of inflammation and metabolism collected prior to scanning. We compared the relationships between peripheral endocrine, metabolic, and immune signaling and brain activity to food cues between depressed participants experiencing increased (N = 23) or decreased (N = 31) appetite and weight in their current depressive episode and healthy control participants (N = 42). The two depression subgroups were unmedicated and did not differ in depression severity, anxiety, anhedonia, or body mass index. Depressed participants experiencing decreased appetite had higher cortisol levels than subjects in the other two groups, and their cortisol values correlated inversely with the ventral striatal response to food cues. In contrast, depressed participants experiencing increased appetite exhibited marked immunometabolic dysregulation, with higher insulin, insulin resistance, leptin, CRP, IL-1RA, and IL-6, and lower ghrelin than subjects in other groups, and the magnitude of their insulin resistance correlated positively with the insula response to food cues. These findings provide novel evidence linking aberrations in homeostatic signaling pathways within depression subtypes to the activity of neural systems that respond to food cues and select when, what, and how much to eat. In conjunction with prior work, the present findings strongly support the existence of pathophysiologically distinct depression subtypes for which the direction of appetite change may be an easily measured behavioral marker.

Indexed as

AppetiteAdolescentAdultC-Reactive ProteinDepressionFemaleGhrelinHumansHydrocortisoneInflammationInsulinInsulin ResistanceInterleukin 1 Receptor Antagonist ProteinInterleukin-6LeptinMaleC-Reactive ProteinGhrelinHydrocortisoneInsulinInterleukin 1 Receptor Antagonist ProteinInterleukin-6Leptin

Identifiers

PMID29899546
PMCPMC6292746
OpenAlexW2808582719

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.