Evidence map›Paper›PMID 37365323›Full record

ReviewNature reviews. Endocrinology2023

Targeting the central melanocortin system for the treatment of metabolic disorders.

Patrick Sweeney, Luis E Gimenez, Ciria C Hernandez, Roger D Cone

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07674290 (Real-World Effectiveness, Safety and Patient-reported Outcomes of Setmelanotide in Patients With Bardet-Biedl Syndrome), which is not on this map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
9.2field-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.

NCT07674290 phase4recruitingnot on this map

Real-World Effectiveness, Safety and Patient-reported Outcomes of Setmelanotide in Patients With Bardet-Biedl Syndrome: A Prospective Mono Centric Observational Interventional Study

TypeinterventionalSponsorTom HühneRan2023 to 2030Enrolled200ConditionsBardet Biedl Syndrome (BBS), Bardet Biedl Syndrome, Bardet-Biedl Syndrome (BBS), Alstrom SyndromeArmsSetmelanotide
3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
  2. Article
  3. The causes of cachexia: key signals and the brain.Nature reviews. Endocrinology · 2026
    Review
  4. Article
  5. Article
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  7. Review
  8. Article
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  10. Review
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  14. Review
  15. Article
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  18. Cancer cachexia: molecular basis and therapeutic advances.Signal transduction and targeted therapy · 2026
    Review
  19. Review
  20. Review
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

4 authors at 2 institutions in 1 country.

Patrick SweeneySchool of Molecular and Cellular Biology, College of Liberal Arts and Sciences, University of Illinois Urbana-Champaign, Champaign, IL, USA.
Luis E GimenezLife Sciences Institute, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-0110-2135
Ciria C HernandezLife Sciences Institute, University of Michigan, Ann Arbor, MI, USA.
Roger D ConeLife Sciences Institute, University of Michigan, Ann Arbor, MI, USA. rcone@umich.edu.ORCID http://orcid.org/0000-0003-3333-5651
University of Michigan · USUniversity of Illinois Urbana-Champaign · US

Funding

Sexually Dimorphic Expression and Function of the Melanocortin-3 ReceptorR01DK126715 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CONE, ROGER D. · 2020 to 2022
$1.0M
MC3R inhibition as a strategy to maintain weight loss in obesityK99DK127065 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SWEENEY, PATRICK · 2020 to 2021
$182k
A role for hypothalamic melanocortin 3 receptors in integrating energy state with reproductive physiologyF32HD095620 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SWEENEY, PATRICK · 2018 to 2020
$158k
NICHD NIH HHS F32 HD095620NIDDK NIH HHS K99 DK127065NIDDK NIH HHS R01 DK126715
6 · The paper itself

Abstract

A large body of preclinical and clinical data shows that the central melanocortin system is a promising therapeutic target for treating various metabolic disorders such as obesity and cachexia, as well as anorexia nervosa. Setmelanotide, which functions by engaging the central melanocortin circuitry, was approved by the FDA in 2020 for use in certain forms of syndromic obesity. Furthermore, the FDA approvals in 2019 of two peptide drugs targeting melanocortin receptors for the treatment of generalized hypoactive sexual desire disorder (bremelanotide) and erythropoietic protoporphyria-associated phototoxicity (afamelanotide) demonstrate the safety of this class of peptides. These approvals have also renewed excitement in the development of therapeutics targeting the melanocortin system. Here, we review the anatomy and function of the melanocortin system, discuss progress and challenges in developing melanocortin receptor-based therapeutics, and outline potential metabolic and behavioural disorders that could be addressed using pharmacological agents targeting these receptors.

Indexed as

Metabolic DiseasesSexual Dysfunctions, PsychologicalCachexiaHumansMelanocortinsObesityMelanocortins

Identifiers

PMID37365323
OpenAlexW4382024145

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.