Cited by 6Lipid metabolism and disordersLipoproteins and Cardiovascular HealthDiabetes, Cardiovascular Risks, and Lipoproteins

The impact of olezarsen on hypertriglyceridemia in high cardiovascular risk patients: a systematic review, meta-analysis, and meta-regression

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Ashraf, Taimoor, Devi, Nisha, Aradhna, Fnu, Devi, Sanjana, Nancy, Fnu, Kumar, Avinash, Ameer, Fiza, Absar, Fnu, Kumar, Laksh, Kumar, Sateesh, Jabbar, Maheen, Jabbar, Fatima, Shahwar Afzal, Dur E., Abdella Yusuf, Salih·2025·Annals of Medicine & Surgery

Abstract

Background and objective: Hypertriglyceridemia is a prevalent lipid disorder that considerably increases the risk of cardiovascular diseases, pancreatitis, and metabolic syndrome. Existing treatment options, including lifestyle changes and medications, often show limited effectiveness and may cause side effects. Olezarsen, an antisense oligonucleotide targeting apolipoprotein C-III (APOC3), represents a novel therapeutic strategy for lowering triglyceride levels. This systematic review and meta-analysis assess the efficacy and safety of olezarsen in comparison to a placebo for managing hypertriglyceridemia. Methods: A systematic literature search was performed in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines across databases such as PubMed, Google Scholar, and the Cochrane Library, incorporating clinical trials and conference proceedings. Studies that compared olezarsen with a placebo and reported outcomes related to triglyceride levels, APOC3, and other lipid parameters were included. Two independent reviewers conducted data extraction and quality assessment. Statistical analyses were performed using RevMan, employing risk ratios for dichotomous variables and standard mean differences for continuous variables, with a random-effects model. Results: Three randomized controlled trials, comprising 334 participants, were included in the analysis. Olezarsen significantly lowered triglyceride levels at both 6 months (standard mean difference [SMD]: -1.69, 95% CI -2.22 to -1.17) and 12 months (SMD: -1.64, 95% CI -2.22 to -1.07). Very low-density lipoprotein (VLDL) levels also declined at 6 months (SMD: -1.95, 95% CI -2.38 to -1.51) and 12 months (SMD: -0.83, 95% CI -1.13 to -0.53). Additional lipid profile improvements included reductions in total cholesterol, non-HDL cholesterol, and apoB levels, along with increases in HDL cholesterol and apoA-1. The incidence of adverse events was similar between the olezarsen and placebo groups. Conclusion: Olezarsen effectively reduces triglyceride and VLDL levels while enhancing lipid profiles in patients with hypertriglyceridemia. Although serious adverse events were more frequent, the overall safety profile remains acceptable. Further long-term research is required to validate these findings and optimize treatment regimens.

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  • Prior systematic reviews and meta-analyses of olezarsen in hypertriglyceridemic or dyslipidemic cohorts were limited by small sample sizes, underpowered individual endpoints, lack of restriction to severe hypertriglyceridemia, and absence of systematic evaluation of pancreatitis as a clinical outcome.

    “Prior systematic reviews and meta-analyses have reported the efficacy of olezarsen in hypertriglyceridemic or dyslipidemic cohorts; however, these studies were limited by small sample sizes, underpowered individual endpoints, lack of restriction to SHTG, and the absence of systematic evaluation of pancreatitis as a clinical outcome [10][11][12][13].”

    From Efficacy of Olezarsen in Severe Hypertriglyceridemia and Acute Pancreatitis Risk: A Systematic Review and Meta-Analysis of Randomized Controlled Trials (2026) · cites this paper as [10]

    In “Limitations and future research” (page unavailable), the review says its three included trials yielded a relatively small sample and restricted statistical power, and that it did not evaluate pancreatitis as a clinical outcome. Its Study selection criteria (page unavailable) do not restrict participants to severe hypertriglyceridemia. The paper does not specifically establish that individual endpoints were underpowered, so that part of the attributed claim goes beyond its findings. (LLM, conf=0.86)

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Authors
Ashraf, T., Devi, N., Aradhna, F., Devi, S., Nancy, F., Kumar, A., Ameer, F., Absar, F., Kumar, L., Kumar, S., Jabbar, M., Jabbar, F., Shahwar Afzal, D. E., & Abdella Yusuf, S.
Affiliations
  • Nishtar Medical College and Hospital (PK)
  • Bahria University (PK)
  • Liaquat National Hospital (PK)
  • Department of Medicine, Indus Medical College, Hyderabad, Pakistan
  • United Medical and Dental College (PK)
  • Liaquat University of Medical & Health Sciences (PK)
  • Department of Medicine, Shaheed Mohtarma Benazir Bhutto Medical College Lyari, Karachi, Pakistan
  • Department of Medicine, Hawassa University, Awasa, Ethopia
Venue
Annals of Medicine & Surgery
Published
2025-06-23
Volume
87
Issue
8
Pages
5173-5184
ISSN
2049-0801 (ISSN-L)
OpenAlex
W4411473094
Cited by
6
References
51
Citations by year
2026: 6
FWCI
1.09
Type
journal article
Language
en
Open access
Locations
  • Annals of Medicine and Surgery (publishedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
  • Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
Keywords
olezarsen, hypertriglyceridemia, apolipoprotein C-III, antisense oligonucleotides, triglyceride lowering, VLDL, lipid profile, cardiovascular risk, drug safety, adverse events, HDL cholesterol, non-HDL cholesterol, apolipoprotein B, apolipoprotein A-I

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