Evidence map›Paper›PMID 23774329›Full record

SynthesisInternational journal of obesity (2005)2014

The melanocortin-4 receptor as target for obesity treatment: a systematic review of emerging pharmacological therapeutic options.

L Fani, S Bak, P Delhanty, E F C van Rossum, E L T van den Akker

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in International journal of obesity (2005), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 119 citations in OpenAlex.

  1. Trial
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  6. Article
  7. Article
  8. Article
  9. Review
  10. Genetics and epigenetics in the obesity phenotyping scenario.Reviews in endocrine & metabolic disorders · 2023
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Network dynamics of hypothalamic feeding neurons.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  18. The central melanocortin system and human obesity.Journal of molecular cell biology · 2020
    Review
  19. Review
  20. Article
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

5 authors at 2 institutions in 1 country.

L FaniDepartment of Pediatrics, Division of Endocrinology, Erasmus MC, Rotterdam, The Netherlands.
S BakDepartment of Pediatrics, Division of Endocrinology, Erasmus MC, Rotterdam, The Netherlands.
P DelhantyDepartment of Internal Medicine, Division of Endocrinology, Erasmus MC, Rotterdam, The Netherlands.
E F C van RossumDepartment of Internal Medicine, Division of Endocrinology, Erasmus MC, Rotterdam, The Netherlands.
E L T van den AkkerDepartment of Pediatrics, Division of Endocrinology, Erasmus MC, Rotterdam, The Netherlands.
Erasmus MC · NLErasmus University Rotterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity is one of the greatest public health challenges of the 21st century. Obesity is currently responsible for ∼0.7-2.8% of a country's health costs worldwide. Treatment is often not effective because weight regulation is complex. Appetite and energy control are regulated in the brain. Melanocortin-4 receptor (MC4R) has a central role in this regulation. MC4R defects lead to a severe clinical phenotype with lack of satiety and early-onset severe obesity. Preclinical research has been carried out to understand the mechanism of MC4R regulation and possible effectors. The objective of this study is to systematically review the literature for emerging pharmacological obesity treatment options. A systematic literature search was performed in PubMed and Embase for articles published until June 2012. The search resulted in 664 papers matching the search terms, of which 15 papers remained after elimination, based on the specific inclusion and exclusion criteria. In these 15 papers, different MC4R agonists were studied in vivo in animal and human studies. Almost all studies are in the preclinical phase. There are currently no effective clinical treatments for MC4R-deficient obese patients, although MC4R agonists are being developed and are entering phase I and II trials.

Indexed as

Acetamidesalpha-MSHAnimalsAnti-Obesity AgentsAppetite RegulationBody Mass IndexEnergy IntakeEnergy MetabolismGene FrequencyGenotypeHumansObesityPeptides, CyclicPhenotypePyrrolidinesReceptor, Melanocortin, Type 4Acetamidesalpha-MSHAnti-Obesity Agentsmelanotan-IIMK-0489N-1-(2-(1-(tert-butyl-4-(2,4-difluorophenyl)pyrrolidin-3-yl)-5-chlorophenyl)ethyl)acetamidePeptides, CyclicPyrrolidinesReceptor, Melanocortin, Type 4Receptors, Cell SurfaceSpiro Compounds

Identifiers

PMID23774329
OpenAlexW2019132602

What OpenQuestion holds

Textmetadata
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.