Evidence map›Paper›PMID 27783055›Full record

ReviewInternational journal of molecular sciences2016

Melatonin as a Potential Agent in the Treatment of Sarcopenia.

Ana Coto-Montes, Jose A Boga, Dun X Tan, Russel J Reiter

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Inflammaging: Implications in Sarcopenia.International journal of molecular sciences · 2022
    Review
  6. Review
  7. Article
  8. Review
  9. The Interactome in the Evolution From Frailty to Sarcopenic Dependence.Frontiers in cell and developmental biology · 2021
    Review
  10. Article
  11. The regulatory role of melatonin in skeletal muscle.Journal of muscle research and cell motility · 2020
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  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

4 authors at 2 institutions in 2 countries.

Ana Coto-MontesDepartment of Morphology and Cellular Biology, Medicine Faculty, University of Oviedo, Julian Claveria, s/n, Oviedo 33006, Spain. acoto@uniovi.es.
Jose A BogaDepartment of Cellular and Structural Biology, UTHSCSA, San Antonio, TX 78229, USA. joseantonio.boga@sespa.es.
Dun X TanDepartment of Cellular and Structural Biology, UTHSCSA, San Antonio, TX 78229, USA. tan@uthscsa.edu.
Russel J ReiterDepartment of Cellular and Structural Biology, UTHSCSA, San Antonio, TX 78229, USA. reiter@uthscsa.edu.
The University of Texas Health Science Center at San Antonio · USUniversidad de Oviedo · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Considering the increased speed at which the world population is aging, sarcopenia could become an epidemic in this century. This condition currently has no means of prevention or treatment. Melatonin is a highly effective and ubiquitously acting antioxidant and free radical scavenger that is normally produced in all organisms. This molecule has been implicated in a huge number of biological processes, from anticonvulsant properties in children to protective effects on the lung in chronic obstructive pulmonary disease. In this review, we summarize the data which suggest that melatonin may be beneficial in attenuating, reducing or preventing each of the symptoms that characterize sarcopenia. The findings are not limited to sarcopenia, but also apply to osteoporosis-related sarcopenia and to age-related neuromuscular junction dysfunction. Since melatonin has a high safety profile and is drastically reduced in advanced age, its potential utility in the treatment of sarcopenic patients and related dysfunctions should be considered.

Indexed as

AgingAnimalsAntioxidantsHumansMelatoninMuscle, SkeletalOsteoporosisSarcopeniaAntioxidantsMelatoninagingfrailtymelatoninsarcopeniaskeletal muscle

Identifiers

PMID27783055
PMCPMC5085795
OpenAlexW2535327071

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.