Evidence map›Paper›PMID 39476283›Full record

ReviewHigh blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension2025

Antisense Oligonucleotides in Dyslipidemia Management: A Review of Clinical Trials.

Ikponmwosa Jude Ogieuhi, Kristen Callender, God-Dowell O Odukudu, Emeka Stanley Obi, Kudzaishe Muzofa, Adetola Emmanuel Babalola, Oshomoh Mark-Anthony Ugiomoh, Kenechukwu Hilary Umenzeakor, Adewunmi Akingbola, Charity Onetemizeh Ayoson and 2 more

Abstract readReview
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In one paragraph

Review in High blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

12 authors.

Ikponmwosa Jude OgieuhiSiberian State Medical University, Tomsk, Russia. Jude.ogieuhi@gmail.com.ORCID http://orcid.org/0009-0003-9465-0089
Kristen CallenderQueen Elizabeth Hospital, Martindales Road, Bridgetown, St. Michael, Barbados.
God-Dowell O OdukuduMorehouse School of Medicine, Atlanta, USA.
Emeka Stanley ObiEast Tennessee State University, Johnson City, USA.
Kudzaishe MuzofaSiberian State Medical University, Tomsk, Russia.
Adetola Emmanuel BabalolaFaculty of Dentistry, CollegeofMedicine, University of Ibadan, Ibadan, Nigeria.
Oshomoh Mark-Anthony UgiomohSiberian State Medical University, Tomsk, Russia.
Kenechukwu Hilary UmenzeakorNnamdi Azikiwe University Teaching Hospital Nnewi, Anambra State, Nnewi, Nigeria.
Adewunmi AkingbolaDepartment of Public Health, University of Cambridge, Cambridge, England, UK.
Charity Onetemizeh AyosonOlabisi Onabanjo University, Ago-Iwoye, Ogun State, Nigeria.
Emmanuel Uchenna AgboSiberian State Medical University, Tomsk, Russia.
Moses Chukwuebuka OdoekeUniversity of Toledo, Toledo, OH, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionElevated serum total cholesterol levels, very low-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triglycerides, or a decreased serum high-density lipoprotein cholesterol concentration characterize dyslipidemia. Antisense Oligonucleotide therapy in dyslipidemia targets apolipoprotein B (ApoB), an essential component of low-density lipoprotein (LDL) associated with atherosclerosis development.

aimThis review aims to critically evaluate the efficacy and safety of this group of medications in mitigating dyslipidemia in at-risk individuals and its potential role in advancing personalized medicine in the management of dyslipidemias.

methodsA detailed search was conducted from multiple databases adhering to the PRISMA guidelines. Clinical trials and randomized controlled trials on antisense oligonucleotides for management of dyslipidemias were included, excluding non-English studies, case reports and all forms of reviews. Data was screened, with duplicates removed, and key findings were synthesized using a narrative approach. RESULTS AND

conclusionThe potential of antisense oligonucleotides (ASOs) to treat dyslipidemia and other disorders has attracted much interest. Several studies and clinical trials have been conducted on the safety and tolerability of ASOs for dyslipidemia. Although statins are the mainstay management of hypercholesterolemia, there is evidence from clinical trials that ASOs can even be more effective with little to no side effects. Novel therapeutic approaches such as antisense oligonucleotides (ASOs) offer tailored therapeutic alternatives. ASOs such as Mipomersen and Volanesorsen provide additional treatment options for patients with inherited lipid abnormalities by lowering certain atherogenic lipoproteins such as apo B and ApoC-III, respectively.

Indexed as

DyslipidemiasHypolipidemic AgentsLipidsOligonucleotides, AntisenseApolipoprotein B-100BiomarkersClinical Trials as TopicHumansTreatment OutcomeAPOB protein, humanApolipoprotein B-100BiomarkersHypolipidemic AgentsLipidsOligonucleotides, AntisenseAntisense oligonucleotidesAtherosclerosisCardiovascular diseasesDyslipidemia

Identifiers

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.