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A Paradigm Shift in Dyslipidemia Management in Primary Care: A 12-Month Cohort Study
Jun Hwa Hong1, Ung Jeon2, Won-Yong Shin2
1Department of Internal Medicine, Eulji University Hospital, School of Medicine, Daejeon, Korea.
Insights
Fixed-dose rosuvastatin and ezetimibe combination therapy effectively lowers LDL-C and improves lipid profiles in intermediate-risk patients. This combination shows better tolerability and fewer adverse events than statin monotherapy for cardiovascular disease prevention.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Preventive Cardiology
Background:
- LDL-lowering therapy is crucial for reducing cardiovascular disease (CVD) risk.
- Higher statin doses effectively lower LDL-C but can increase adverse events like muscle issues and new-onset diabetes mellitus (DM).
- Combining ezetimibe with statins improves LDL-C reduction and tolerability in patients with existing CVD.
Purpose of the Study:
- To evaluate the efficacy and safety of a fixed-dose rosuvastatin and ezetimibe (R+E) combination therapy.
- To assess the impact of R+E on lipid profiles (LDL-C, HDL-C, triglycerides) in intermediate-risk patients without DM.
- To compare the 12-month outcomes of R+E combination therapy with statin monotherapy in a primary care setting.
Main Methods:
- A multicenter, prospective observational study involving 5717 patients in Korean primary healthcare centers.
- Propensity score matching was used to analyze a subset of 700 patients.
- Patients received either statin monotherapy or a fixed-dose combination of ezetimibe (10 mg) with rosuvastatin (5, 10, or 20 mg).
Main Results:
- Fixed-dose R+E significantly reduced LDL-C more than statin monotherapy across all dosages (29.35%–41.83% vs. 19.09%).
- HDL-C levels increased with 5/10 mg R+E, and triglyceride levels decreased with 10/10 mg R+E compared to statin monotherapy.
- The R+E combination therapy demonstrated fewer adverse events and a neutral effect on glucose metabolism compared to statin monotherapy at 12 months.
Conclusions:
- Fixed-dose rosuvastatin and ezetimibe combination therapy offers potent LDL-lowering efficacy and improved tolerability.
- This combination may represent a beneficial option for primary cardiovascular prevention in intermediate-risk patients.
- Further large-scale prospective studies are warranted to confirm these findings.
Purpose:
LDL-lowering therapy is beneficial to reduce the risk of cardiovascular disease (CVD). Higher statin doses lower LDL-C levels and prevent CVD; however, they increase adverse events, such as muscle-related adverse events and new-onset diabetes mellitus (DM). Ezetimibe combined with statin therapy improves LDL-C-lowering levels and tolerability in patients with established CVD. We aimed to analyze the efficacy and safety of a fixed-dose rosuvastatin and ezetimibe (R+E) combination therapy in intermediate-risk patients with hypercholesterolemia and no DM after 12 months of visiting a primary physician.
Methods:
This multicenter, open-label, single-arm, prospective observational study involved 5717 patients from 258 primary health care centers in Korea enrolled between 2016 and 2018. Patients had no DM or previous CVD but had cardiovascular risk factors and were taking a statin or a fixed-dose combination of E (10 mg) + R (5, 10, or 20 mg). We analyzed 700 patients using propensity score matching.
Findings:
A fixed-dose R+E combination therapy significantly reduced LDL-C in 5/10 mg R+E (29.35%), 10/10 mg R+E (36.19%), and 20/10 mg R+E (41.83%) compared with statin monotherapy (19.09%) at 12-month follow-up (P = 0.017). Compared with statin monotherapy, HDL-C levels increased in 5/10 mg R+E (mean change at 12 months; P = 0.004), and triglyceride levels decreased in 10/10 mg R+E (mean change at 12 months; P = 0.033). The fixed-dose R+E combination therapy was associated with fewer adverse events and a neutral effect on glucose deterioration compared with statin monotherapy at 12 months of follow-up.
Implications:
In a possible paradigm shift, a fixed-dose R+E combination therapy may be beneficial for primary cardiovascular prevention with potent LDL-lowering efficacy and tolerability; however, further large prospective studies are needed.
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