Evidence map›Paper›PMID 34607230›Full record

ArticleInternational immunopharmacology2021

The role of lovastatin in the attenuation of COVID-19.

Sajad Karampoor, Khashayar Hesamizadeh, Zinat Shams, Arefeh Ghafari Novin, Mohammad Farahmand, Hamid Zahednasab, Rasoul Mirzaei, Farhad Zamani, Marzieh Hajibaba, Behnaz Bouzari and 4 more

Open access · greenAbstract read
In one paragraph

Article in International immunopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  4. Article
  5. Article
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  7. Statins: Beneficial Effects in Treatment of COVID-19.Advances in experimental medicine and biology · 2023
    Article
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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

14 authors at 7 institutions in 1 country.

Sajad KarampoorGastrointestinal and Liver Diseases Research Center, Iran University of Medical Sciences, Tehran, Iran; Department of Virology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran. Electronic address: karampour.s@iums.ac.ir.
Khashayar HesamizadehDepartment of Virology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran; Middle East Liver Diseases (MELD) Center, Tehran, Iran.
Zinat ShamsDepartment of Biological Science, Kharazmi University, Tehran, Iran.
Arefeh Ghafari NovinDepartment of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Mohammad FarahmandDepartment of Medical Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Hamid ZahednasabInstitute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran.
Rasoul MirzaeiDepartment of Microbiology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Farhad ZamaniGastrointestinal and Liver Diseases Research Center, Iran University of Medical Sciences, Tehran, Iran.
Marzieh HajibabaGastrointestinal and Liver Diseases Research Center, Iran University of Medical Sciences, Tehran, Iran.
Behnaz BouzariDepartment of Pathology, Firouzgar Hospital, Iran University of Medical Sciences, Tehran, Iran.
Azadeh LaaliDepartment of Infectious Disease, School of Medicine, Firoozgar General Hospital, Iran University of Medical Sciences, Tehran, Iran.
Alireza TabibzadehDepartment of Virology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mohammad Hadi Karbalaie NiyaGastrointestinal and Liver Diseases Research Center, Iran University of Medical Sciences, Tehran, Iran.
Hossein KeyvaniGastrointestinal and Liver Diseases Research Center, Iran University of Medical Sciences, Tehran, Iran; Department of Virology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran. Electronic address: keyvani.h@iums.ac.ir.
Iran University of Medical Sciences · IRFiroozgar General Hospital · IRTehran University of Medical Sciences · IRHamedan University of Medical Sciences · IRKharazmi University · IRMiddle East Liver Disease Center · IRUniversity of Tehran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mounting evidence regarding the pathogenesis of COVID-19 indicated that the cytokine storm has an axial role in the severity of this disease, which may lead to thrombotic complications, acute respiratory distress syndrome (ARDS), and myocardial damage, among other consequences. It has recently been demonstrated that statins are known to have anti-viral, anti-inflammatory, anti-thrombotic, and immunomodulatory features; however, their advantage has not been evaluated in COVID-19. This study aimed to investigate the protective effects of lovastatin in intensive care unit (ICU) patients with COVID-19. The case-control study consists of 284 ICU patients, which classified into three groups as follows: 1) the patients who no received lovastatin as a control (92 patients), 2) patients received 20 mg per day lovastatin (99 patients), and 3) patients received 40 mg per day lovastatin (93 patients). Each group's demographic and clinical parameters, along with CRP, interleukin (IL)-6, IL-8 levels, and mortality rate, were studied in three-time points. The results showed that there was no statistically significant difference between our study groups in terms of age and sex. (P > 0.05). Besides, in patients, receiving lovastatin the CRP, IL-6, IL-8 levels were significantly decreased from T1 to T3 than to the control group. Our results also showed that the use of lovastatin in COVID-19 patients significantly reduced the length of hospitalization in the ICU compared with the control group. In addition, our results showed that the mortality rate in patients receiving lovastatin was lower when compared to the control group; however, this difference was not statistically significant. Since the cytokine storm is a significant factor in the pathology of SARS-CoV-2, our findings highlighted the potential use of lovastatin to mitigate the inflammatory response induced by SARS-CoV-2 infection.

Indexed as

COVID-19 Drug TreatmentAdultAnti-Inflammatory AgentsCase-Control StudiesCOVID-19Critical CareCytokine Release SyndromeCytokinesFemaleHospitalizationHumansIntensive Care UnitsInterleukin-6Interleukin-8LovastatinMaleAnti-Inflammatory AgentsCRP protein, humanCXCL8 protein, humanCytokinesIL6 protein, humanInterleukin-6Interleukin-8LovastatinReceptors, ImmunologicCOVID-19ICUInflammationLovastatinSARS-CoV-2Statin

Identifiers

PMID34607230
PMCPMC8461262
OpenAlexW3204547441

What Socratic 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 Socratic graph.