Evidence map›Paper›PMID 28534160›Full record

ReviewClinical reviews in allergy & immunology2018

MicroRNAs: New Therapeutic Targets for Familial Hypercholesterolemia?

Amir Abbas Momtazi, Maciej Banach, Matteo Pirro, Evan A Stein, Amirhossein Sahebkar

Open access · hybridFull text readReview
In one paragraph

Review in Clinical reviews in allergy & immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Review
  3. Small interfering RNA effect on lipoprotein(a): a systematic review.The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology · 2025
    Review
  4. Article
  5. Article
  6. Article
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  8. Article
  9. Review
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  11. An Update on the Role of PCSK9 in Atherosclerosis.Journal of atherosclerosis and thrombosis · 2020
    Review
  12. Review
  13. Article
  14. Article
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  17. 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

5 authors at 4 institutions in 5 countries.

Amir Abbas MomtaziNanotechnology Research Center, Department of Medical Biotechnology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Maciej BanachDepartment of Hypertension, WAM University Hospital in Lodz, Medical University of Lodz (MUL), Zeromskiego 113, 90-549, Lodz, Poland. maciejbanach77@gmail.com.ORCID http://orcid.org/0000-0001-6690-6874
Matteo PirroUnit of Internal Medicine, Angiology and Arteriosclerosis Diseases, Department of Medicine, University of Perugia, Perugia, Italy.
Evan A SteinMetabolic and Atherosclerosis Research Center, Cincinnati, OH, USA.
Amirhossein SahebkarBiotechnology Research Center, Mashhad University of Medical Sciences, Mashhad, 9177948564, Iran. amirhossein.sahebkar@uwa.edu.au.
Mashhad University of Medical Sciences · IRLouisville Metabolic and Atherosclerosis Research Center · USMedical University of Lodz · PLUniversity of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial hypercholesterolemia (FH) is the most common inherited form of dyslipidemia and a major cause of premature cardiovascular disease. Management of FH mainly relies on the efficiency of treatments that reduce plasma low-density lipoprotein (LDL) cholesterol (LDL-C) concentrations. MicroRNAs (miRs) have been suggested as emerging regulators of plasma LDL-C concentrations. Notably, there is evidence showing that miRs can regulate the post-transcriptional expression of genes involved in the pathogenesis of FH, including LDLR, APOB, PCSK9, and LDLRAP1. In addition, many miRs are located in genomic loci associated with abnormal levels of circulating lipids and lipoproteins in human plasma. The strong regulatory effects of miRs on the expression of FH-associated genes support of the notion that manipulation of miRs might serve as a potential novel therapeutic approach. The present review describes miRs-targeting FH-associated genes that could be used as potential therapeutic targets in patients with FH or other severe dyslipidemias.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsApolipoproteins BCardiovascular DiseasesCholesterolDyslipidemiasGene Expression RegulationHumansHyperlipoproteinemia Type IILipid MetabolismMicroRNAsMolecular Targeted TherapyProprotein Convertase 9Receptors, LDLAdaptor Proteins, Signal TransducingApolipoproteins BCholesterolLDLRAP1 protein, humanLDLR protein, humanMicroRNAsPCSK9 protein, humanProprotein Convertase 9Receptors, LDLApolipoprotein BLDLRAP1LDL receptorLow-density lipoprotein cholesterolmicroRNAPCSK9

Identifiers

PMID28534160
PMCPMC5874276
OpenAlexW2617061545

What OpenQuestion holds

Textfull text, public
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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.