Advances in treatment of Dyslipidemia
Open accessAbstract
Dyslipidemias have emerged as prevalent disorders among patients, posing significant risks for the development and progression of cardiovascular diseases. These conditions are characterized by elevated levels of total cholesterol (TC), triglycerides (TGs), and low-density lipoprotein cholesterol (LDL-C). This review delves into the current treatment approach, focusing on equalizing these parameters while enhancing the overall quality of life for patients. Through an extensive analysis of clinical trials, we identify disorders that necessitate alternative treatment strategies, notably familial hypercholesterolemia. The primary objective of this review is to consolidate existing information concerning drugs with the potential to revolutionize dyslipidemia management significantly. Among these promising pharmaceuticals, we highlight alirocumab, bempedoic acid, antisense oligonucleotides, angiopoietin-like protein inhibitors, apolipoprotein C-III (APOC3) inhibitors, lomitapide, and cholesterol ester transfer protein (CETP) inhibitors. Our review demonstrates the pivotal roles played by each of these drugs in targeting specific parameters of lipid metabolism. We outline the future landscape of dyslipidemia treatment, envisaging a more tailored and effective therapeutic approach to address this widespread medical concern.
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Clinical evidence supports the occurrence of specific adverse effects associated with most lipid-lowering drugs.
“clinical evidence supports the occurrence of specific adverse effects associated with most lipid-lowering drugs (Dybiec et al., 2023).”
From Lactiplantibacillus plantarum N4 ameliorates lipid metabolism and gut microbiota structure in high fat diet-fed rats (2024) · cites this paper as Dybiec et al., 2023
Section 5 reports clinical evidence of specific adverse effects for statins and reports adverse events with alirocumab, volanesorsen, and lomitapide (pages unavailable). This supports the claim for several lipid-lowering drugs, but the review does not establish that such effects occur with most of them; it reports no significant adverse effects for anacetrapib. (LLM, conf=0.83)
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- Authors
- Dybiec, J., Baran, W., Dąbek, B., Fularski, P., Młynarska, E., Radzioch, E., Rysz, J., & Franczyk, B.
- Affiliations
- Medical University of Lodz (PL)
- Corresponding author
- Młynarska, Ewelina
- ORCID
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2023-08-27
- Volume
- 24
- Issue
- 17
- Pages
- 13288
- ISSN
- 1422-0067 (ISSN-L)
- PMC
- PMC10488025
- OpenAlex
- W4386222220
- Cited by
- 55
- References
- 111
- Citations by year
- 2026: 19 · 2025: 23 · 2024: 11 · 2023: 2
- FWCI
- 3.56
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- International Journal of Molecular Sciences (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Keywords
- dyslipidemia, lipid-lowering therapy, PCSK9 inhibitors, alirocumab, bempedoic acid, antisense oligonucleotides, lomitapide, CETP inhibitors, familial hypercholesterolemia, cardiovascular risk, LDL cholesterol, triglycerides, total cholesterol
- MeSH terms
- Angiopoietin-like Proteins, Humans, Cholesterol, LDL, Quality of Life, Dyslipidemias, Apolipoprotein C-III
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