Evidence map›Paper›PMID 20004082›Full record

ReviewNutrition (Burbank, Los Angeles County, Calif.)2010

Update on melanocortin interventions for cachexia: progress toward clinical application.

Mark Daniel DeBoer

Open access · greenAbstract readReview
In one paragraph

Review in Nutrition (Burbank, Los Angeles County, Calif.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-weighted citation impact, top 25% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Cachexia: Pathophysiology and Ghrelin Liposomes for Nose-to-Brain Delivery.International journal of molecular sciences · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. Pathophysiology of anorexia in the cancer cachexia syndrome.Journal of cachexia, sarcopenia and muscle · 2015
    Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Cancer cachexia: mechanisms and clinical implications.Gastroenterology research and practice · 2011
    Article
  19. Neuropeptides in the pathophysiology and treatment of cachexia.Current opinion in supportive and palliative care · 2010
    Review
  20. Animal models of anorexia and cachexia.Expert opinion on drug discovery · 2009
    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

1 author at 1 institution in 1 country.

Mark Daniel DeBoerDivision of Pediatric Endocrinology, University of Virginia, Charlottesville, Virginia, USA. deboer@virginia.edu
University of Virginia · US

Funding

Inflammatory Mechanisms of Puberty Dysregulation in ColitisK08HD060739 · NICHD · UNIVERSITY OF VIRGINIA · PI DEBOER, MARK DANIEL · 2009 to 2013
$649k
NICHD NIH HHS K08 HD060739
6 · The paper itself

Abstract

Cachexia is a devastating syndrome of body wasting that is associated with multiple common chronic diseases including cancer, chronic kidney disease, and chronic heart failure. These underlying diseases are associated with increased levels of inflammatory cytokines and result in anorexia, increased resting energy expenditure, and loss of fat and lean body mass. Prior experiments have implicated the central melanocortin system in the hypothalamus with the propagation of these symptoms of cachexia. Pharmacologic blockade of this system using melanocortin antagonists causes attenuation of the signs of cachexia in laboratory models. Recent advances in our knowledge of this disease process have involved further elucidation of the pathophysiology of melanocortin activation and demonstration of the efficacy of melanocortin antagonists in new models of cachexia, including cardiac cachexia. In addition, small molecule antagonists of the melanocortin-4 receptor continue to be introduced, including ones with oral bioavailability. These developments generate optimism that melanocortin antagonism will be used to treat humans with disease-associated cachexia. However, to date, human application has remained elusive and it is unclear when we will know whether humans with cachexia would benefit from treatment with these compounds.

Indexed as

AnimalsAnorexiaCachexiaDisease Models, AnimalHumansHypothalamusMelanocortinsReceptor, Melanocortin, Type 4MelanocortinsReceptor, Melanocortin, Type 4

Identifiers

PMID20004082
PMCPMC2818056
OpenAlexW2171540339

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.