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Effectiveness and Safety of Very-Low-Dose Rosuvastatin-Ezetimibe Therapy in Korean Patients with Dyslipidaemia: A Multicentre Prospective Observational Study

Authors
 Roh, Ji Woong  ;  Park, Moon-hwa  ;  Son, Ji-won  ;  Bae, Sunga 
Citation
 CLINICAL DRUG INVESTIGATION, Vol.45(10) : 803-813, 2025-10 
Journal Title
 CLINICAL DRUG INVESTIGATION 
ISSN
 1173-2563 
Issue Date
2025-10
MeSH
Adult ; Aged ; Anticholesteremic Agents* / administration & dosage ; Anticholesteremic Agents* / adverse effects ; Cholesterol, LDL / blood ; Dose-Response Relationship, Drug ; Drug Therapy, Combination ; Dyslipidemias* / blood ; Dyslipidemias* / drug therapy ; Ezetimibe* / administration & dosage ; Ezetimibe* / adverse effects ; Ezetimibe* / therapeutic use ; Female ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors / administration & dosage ; Hydroxymethylglutaryl-CoA Reductase Inhibitors / adverse effects ; Male ; Middle Aged ; Prospective Studies ; Republic of Korea ; Rosuvastatin Calcium* / administration & dosage ; Rosuvastatin Calcium* / adverse effects ; Rosuvastatin Calcium* / therapeutic use ; Treatment Outcome
Abstract
Background and Objectives Dyslipidaemia is a key modifiable risk factor for atherosclerotic cardiovascular disease. However, achieving recommended low-density lipoprotein cholesterol (LDL-C) target levels is challenging owing to dose-dependent adverse effects and limited tolerability of high-dose statins. This study evaluated the real-world efficacy and safety of combining very-low-dose rosuvastatin (2.5 mg) with ezetimibe (10 mg) in adult patients with dyslipidaemia across different cardiovascular risk strata. Methods This multicentre prospective study in South Korea enrolled 2,388 patients. Participants were stratified into low-, moderate-, or high-risk groups on the basis of the 2019 European Society of Cardiology and European Atherosclerosis Society guidelines. Lipid profiles and safety outcomes were assessed at baseline and after 12 weeks. The primary and secondary outcomes were LDL-C and non-high-density lipoprotein cholesterol (non-HDL-C) target level achievements, respectively, and adverse events were monitored. Results After 12 weeks, LDL-C target levels were achieved by 82.6% of low-risk (< 116 mg/dL), 73.9% of moderate-risk (< 100 mg/dL), and 50.4% of high-risk (< 70 mg/dL) patients. Non-HDL-C target level achievement followed a similar trend. Combination therapy with ezetimibe and low-dose statin resulted in significant LDL-C reductions, compared with statins alone. Adverse events were infrequent (0.6%), and only 0.2% of patients discontinued treatment owing to medication-related concerns. Conclusions Very-low-dose rosuvastatin-ezetimibe combination therapy significantly lowered LDL-C levels and improved lipid profiles across various risk groups, demonstrating a favourable safety profile. These findings support its use as an effective, well-tolerated option for managing dyslipidaemia. Longer-term studies are warranted to evaluate sustained lipid control and cardiovascular outcomes.
Full Text
https://link.springer.com/article/10.1007/s40261-025-01482-3
DOI
10.1007/s40261-025-01482-3
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Roh, Ji Woong(노지웅)
Bae, SungA(배성아) ORCID logo https://orcid.org/0000-0003-1484-4645
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/208352
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