Evidence map›Paper›PMID 35187603›Full record

ReviewCellular and molecular life sciences : CMLS2022

Melatonin: highlighting its use as a potential treatment for SARS-CoV-2 infection.

Russel J Reiter, Ramaswamy Sharma, Fedor Simko, Alberto Dominguez-Rodriguez, Jan Tesarik, Richard L Neel, Andrzej T Slominski, Konrad Kleszczynski, Verna M Martin-Gimenez, Walter Manucha and 1 more

Open access · hybridAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
4.2field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  5. Evolutionary formation of melatonin and vitamin D in early life forms: insects take centre stage.Biological reviews of the Cambridge Philosophical Society · 2024
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  18. Melatonin as a Potential Approach to Anxiety Treatment.International journal of molecular sciences · 2022
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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

11 authors at 8 institutions in 5 countries.

Russel J ReiterDepartment of Cell Systems and Anatomy, UT Health San Antonio, Long School of Medicine, San Antonio, TX, USA. reiter@uthscsa.edu.ORCID http://orcid.org/0000-0001-6763-4225
Ramaswamy SharmaDepartment of Cell Systems and Anatomy, UT Health San Antonio, Long School of Medicine, San Antonio, TX, USA. sharmar3@uthscsa.edu.
Fedor SimkoInstitute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic.
Alberto Dominguez-RodriguezDepartment of Cardiology, Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain.
Jan TesarikMARGen Clinic, 18006, Granada, Spain.
Richard L NeelCEO, Alcasian Care Enterprises, Castroville, TX, USA.
Andrzej T SlominskiDepartment of Dermatology, University of Alabama at Birmingham, Birmingham, AL, USA.
Konrad KleszczynskiDepartment of Dermatology, University of Münster, Münster, Germany.
Verna M Martin-GimenezInstituto de Investigaciones en Ciencias Químicas, Facultad de Cs. Químicas Y Tecnológicas, Universidad Católica de Cuyo, San Juan, Argentina.
Walter ManuchaInstituto de Investigaciones en Ciencias Químicas, Facultad de Cs. Químicas Y Tecnológicas, Universidad Católica de Cuyo, San Juan, Argentina.
Daniel P CardinaliFaculty of Medical Sciences, Pontificia Universidad Católica Argentina, Buenos Aires, Argentina.
The University of Texas Health Science Center at San Antonio · USComenius University Bratislava · SKHospital Universitario de Canarias · ESPontificia Universidad Católica Argentina · ARUniversidad Católica de Cuyo · ARUniversidad Nacional de Cuyo · ARUniversity of Alabama at Birmingham · USUniversity of Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Numerous pharmaceutical drugs have been repurposed for use as treatments for COVID-19 disease. These drugs have not consistently demonstrated high efficacy in preventing or treating this serious condition and all have side effects to differing degrees. We encourage the continued consideration of the use of the antioxidant and anti-inflammatory agent, melatonin, as a countermeasure to a SARS-CoV-2 infection. More than 140 scientific publications have identified melatonin as a likely useful agent to treat this disease. Moreover, the publications cited provide the rationale for the use of melatonin as a prophylactic agent against this condition. Melatonin has pan-antiviral effects and it diminishes the severity of viral infections and reduces the death of animals infected with numerous different viruses, including three different coronaviruses. Network analyses, which compared drugs used to treat SARS-CoV-2 in humans, also predicted that melatonin would be the most effective agent for preventing/treating COVID-19. Finally, when seriously infected COVID-19 patients were treated with melatonin, either alone or in combination with other medications, these treatments reduced the severity of infection, lowered the death rate, and shortened the duration of hospitalization. Melatonin's ability to arrest SARS-CoV-2 infections may reduce health care exhaustion by limiting the need for hospitalization. Importantly, melatonin has a high safety profile over a wide range of doses and lacks significant toxicity. Some molecular processes by which melatonin resists a SARS-CoV-2 infection are summarized. The authors believe that all available, potentially beneficial drugs, including melatonin, that lack toxicity should be used in pandemics such as that caused by SARS-CoV-2.

Indexed as

COVID-19 Drug TreatmentAntioxidantsAntiviral AgentsCOVID-19HumansMelatoninSARS-CoV-2AntioxidantsAntiviral AgentsMelatoninCoronavirusCOVID-19Cytokine stormHypoxia-inducible factor 1-αPhospholipase A2SepsisViral infection

Identifiers

PMID35187603
PMCPMC8858600
OpenAlexW4212880570

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.