Evidence map›Paper›PMID 33953838›Full record

ReviewOxidative medicine and cellular longevity2021

Therapeutic Value of miRNAs in Coronary Artery Disease.

Md Sayed Ali Sheikh, A Alduraywish, A Almaeen, Mubarak Alruwali, Raed Alruwaili, Basil Mohammed Alomair, Umme Salma, Gomaa Mostafa Hedeab, Najeebullah Bugti, Ibrahim A M Abdulhabeeb

Open access · hybridAbstract readReview
In one paragraph

Review in Oxidative medicine and cellular longevity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
2.4field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Review
  5. Article
  6. Impact of microRNAs on cardiovascular diseases and aging.The Journal of international medical research · 2024
    Review
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  8. 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

10 authors at 2 institutions in 2 countries.

Md Sayed Ali SheikhDepartment of Internal Medicine, College of Medicine, Jouf University, Sakaka, Saudi Arabia.ORCID https://orcid.org/0000-0001-7187-6550
A AlduraywishDepartment of Internal Medicine, College of Medicine, Jouf University, Sakaka, Saudi Arabia.
A AlmaeenDepartment of Pathology, College of Medicine, Jouf University, Sakaka, Saudi Arabia.
Mubarak AlruwaliDepartment of Internal Medicine, College of Medicine, Jouf University, Sakaka, Saudi Arabia.
Raed AlruwailiDepartment of Internal Medicine, College of Medicine, Jouf University, Sakaka, Saudi Arabia.
Basil Mohammed AlomairDepartment of Internal Medicine, College of Medicine, Jouf University, Sakaka, Saudi Arabia.
Umme SalmaDepartment of Gynecology and Obstetrics, College of Medicine, Jouf University, Sakaka, Saudi Arabia.
Gomaa Mostafa HedeabDepartment of Pharmacology, College of Medicine, Jouf University, Sakaka, Saudi Arabia.
Najeebullah BugtiCardiac Center, King Abdul Aziz Specialized Hospital, Sakaka, Saudi Arabia.
Ibrahim A M AbdulhabeebCardiac Center, King Abdul Aziz Specialized Hospital, Sakaka, Saudi Arabia.
Jouf University · SABeni-Suef University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atherosclerotic ischemic coronary artery disease (CAD) is a significant community health challenge and the principal cause of morbidity and mortality in both developed and developing countries for all ethnic groups. The progressive chronic coronary atherosclerosis is the main underlying cause of CAD. Although enormous progress occurred in the last three decades in the management of cardiovascular diseases, the prevalence of CAD continues to increase worldwide, indicating the need for discovery of deeper molecular insights of CAD mechanisms, biomarkers, and innovative therapeutic targets. Recently, several research groups established that microRNAs essentially regulate various cardiovascular development and functions, and a deregulated cardiac enriched microRNA profile plays a vital role in the pathogenesis of CAD and its biological aging. Numerous studies established that over- or downregulation of a single miRNA gene by ago-miRNA or anti-miRNA is enough to modify the CAD disease process, significantly prevent age-dependent cardiac cell death, and markedly improve cardiac function. In the light of more recent experimental and clinical evidences, we briefly reviewed and discussed the involvement of miRNAs in CAD and their possible diagnostic/therapeutic values. Moreover, we also focused on the role of miRNAs in the initiation and progression of the atherosclerosis plaque as the strongest risk factor for CAD.

Indexed as

AgedCoronary Artery DiseaseHumansMicroRNAsMicroRNAs

Identifiers

PMID33953838
PMCPMC8057887
OpenAlexW3155439898

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.