Evidence map›Paper›PMID 39940794›Full record

ReviewInternational journal of molecular sciences2025

Novel RNA-Based Therapies in the Management of Dyslipidemias.

Constantine E Kosmas, Maria D Bousvarou, Donatos Tsamoulis, Maria Gianniou, Evangelia J Papakonstantinou, Loukianos S Rallidis

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Zerlasiran for Lipoprotein(a) Reduction: Mechanisms, Evidence, and Future Directions.Cardiovascular & hematological disorders drug targets · 2026
    Review
  7. Article
  8. Review
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

6 authors.

Constantine E Kosmas2nd Department of Cardiology, National & Kapodistrian University of Athens, 12462 Athens, Greece.
Maria D BousvarouHealth Center of Sofades, 43300 Karditsa, Greece.
Donatos Tsamoulis2nd Department of Cardiology, National & Kapodistrian University of Athens, 12462 Athens, Greece.ORCID 0000-0001-8752-1869
Maria GianniouSchool of Medicine, University of Patras, 26504 Rio, Greece.
Evangelia J PapakonstantinouGeneral Directorate of Public Health and Social Welfare, Attica Region, 11521 Athens, Greece.
Loukianos S Rallidis2nd Department of Cardiology, National & Kapodistrian University of Athens, 12462 Athens, Greece.ORCID 0000-0002-7349-0309

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pharmaceutical advancements and an improved understanding of pathophysiology have enabled innovative therapies for chronic conditions like dyslipidemia. This condition is marked by abnormalities in lipid homeostasis. Nucleic acid therapeutics, including antisense oligonucleotides and small interfering RNAs, are novel management strategies that silence genes by targeting mRNA. Antisense oligonucleotides modify mRNA to inhibit protein production, whereas small interfering RNAs induce mRNA degradation via the RNA-induced silencing complex (RISC), thus offering promising treatments for dyslipidemia and atherosclerotic cardiovascular disease. Chemical modifications improve their stability and mRNA targeting. RNA-based therapies targeting PCSK9, Lp(a), ApoC-III, and ANGPTL3 hold transformative potential for treating dyslipidemia effectively. This article discusses the latest data from completed and ongoing trials on RNA therapies for dyslipidemia, including inclisiran, pelacarsen, olpasiran, zerlasiran, lepodisiran, volanesorsen, olezarsen, plozasiran, zodasiran, and solbinsiran. Each therapy targets specific molecules while also significantly impacting other lipid parameters. The promising results of these trials indicate potential improvements in lipid therapy and cardiovascular risk reduction, with ongoing studies expected to further refine the role of the novel RNA-based agents in effective lipid management.

Indexed as

DyslipidemiasGenetic TherapyRNA, Small InterferingAngiopoietin-Like Protein 3AnimalsHumansOligonucleotides, AntisenseProprotein Convertase 9Angiopoietin-Like Protein 3Oligonucleotides, AntisenseProprotein Convertase 9RNA, Small Interferingangiopoietin-like protein 3 (ANGPTL3)antisense oligonucleotides (ASOs)apolipoprotein C-III (ApoC-III)cardiovascular riskdyslipidemialipoprotein(a) [Lp(a)]proprotein convertase subtilisin/kexin type 9 (PCSK9)small interfering RNAs (siRNAs)

Identifiers

PMID39940794
PMCPMC11817214

What OpenQuestion holds

Texttitle and abstract
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.