Evidence map›Paper›PMID 33767443›Full record

ArticleNature metabolism2021

A genetic map of the mouse dorsal vagal complex and its role in obesity.

Mette Q Ludwig, Wenwen Cheng, Desiree Gordian, Julie Lee, Sarah J Paulsen, Stine N Hansen, Kristoffer L Egerod, Pernille Barkholt, Christopher J Rhodes, Anna Secher and 4 more

Open access · greenAbstract read
In one paragraph

Article in Nature metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed
9.9field-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

111 citing papers in PubMed, 162 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Amylin: A Multi-Functional Pancreatic Hormone-A Review.Diabetes, obesity & metabolism · 2026
    Review
  6. The evolving landscape of obesity pharmacotherapy.Nature reviews. Drug discovery · 2026
    Review
  7. Article
  8. The critical role of gut-brain signalling in eating behaviour and obesity.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Functional segregation of body-brain signals in the area postrema.bioRxiv : the preprint server for biology · 2026
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Vagal GABAergic signaling in autonomic control of cardiometabolic function.American journal of physiology. Cell physiology · 2026
    Review

51 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

14 authors at 5 institutions in 2 countries.

Mette Q LudwigNovo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-7814-3859
Wenwen ChengDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-5462-8245
Desiree GordianDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
Julie LeeNovo Nordisk Foundation Center for Stem Cell Biology, University of Copenhagen, Copenhagen, Denmark.
Sarah J PaulsenGlobal Drug Discovery, Novo Nordisk A/S, Måløv, Denmark.
Stine N HansenGlobal Drug Discovery, Novo Nordisk A/S, Måløv, Denmark.
Kristoffer L EgerodNovo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-2781-1594
Pernille BarkholtGubra, Hørsholm, Denmark.ORCID http://orcid.org/0000-0002-3603-2915
Christopher J RhodesResearch and Early Development, Cardiovascular, Renal and Metabolic Diseases, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, USA.ORCID http://orcid.org/0000-0002-7450-1110
Anna SecherGlobal Drug Discovery, Novo Nordisk A/S, Måløv, Denmark.ORCID http://orcid.org/0000-0002-6276-5389
Lotte Bjerre KnudsenGlobal Drug Discovery, Novo Nordisk A/S, Måløv, Denmark.ORCID http://orcid.org/0000-0002-2439-7116
Charles PykeGlobal Drug Discovery, Novo Nordisk A/S, Måløv, Denmark.
Martin G MyersDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
Tune H PersNovo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark. tune.pers@sund.ku.dk.ORCID http://orcid.org/0000-0003-0207-4831
Novo Nordisk (Denmark) · DKUniversity of Copenhagen · DKUniversity of Michigan · USAstraZeneca (United States) · USGubra (Denmark) · DK

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI ROHIT N. KULKARNI · 1986 to 2026
$50.5M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Scott Soleimanpour · 2013 to 2026
$24.3M
Project 3: Neural mediators in the metabolic effects of Vertical Sleeve GastrectomyP01DK117821 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OLSON, DAVID P · 2019 to 2023
$9.3M
NIDDK NIH HHS P01 DK117821NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK036836
6 · The paper itself

Abstract

The brainstem dorsal vagal complex (DVC) is known to regulate energy balance and is the target of appetite-suppressing hormones, such as glucagon-like peptide 1 (GLP-1). Here we provide a comprehensive genetic map of the DVC and identify neuronal populations that control feeding. Combining bulk and single-nucleus gene expression and chromatin profiling of DVC cells, we reveal 25 neuronal populations with unique transcriptional and chromatin accessibility landscapes and peptide receptor expression profiles. GLP-1 receptor (GLP-1R) agonist administration induces gene expression alterations specific to two distinct sets of Glp1r neurons-one population in the area postrema and one in the nucleus of the solitary tract that also expresses calcitonin receptor (Calcr). Transcripts and regions of accessible chromatin near obesity-associated genetic variants are enriched in the area postrema and the nucleus of the solitary tract neurons that express Glp1r and/or Calcr, and activating several of these neuronal populations decreases feeding in rodents. Thus, DVC neuronal populations associated with obesity predisposition suppress feeding and may represent therapeutic targets for obesity.

Indexed as

Chromosome MappingAnimalsAppetiteBody WeightBrain StemCalcitonin Receptor-Like ProteinCell NucleusChromatinGene ExpressionGlucagon-Like Peptide-1 ReceptorHumansMaleMiceMice, Inbred C57BLMice, TransgenicNeuronsCalcitonin Receptor-Like ProteinCalcrl protein, mouseChromatinGlp1r protein, mouseGlucagon-Like Peptide-1 Receptor

Identifiers

PMID33767443
PMCPMC12009600
OpenAlexW3137550402

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.