Effectiveness of low-intensity atorvastatin 5 mg and ezetimibe 10 mg combination therapy compared with moderate-intensity atorvastatin 10 mg monotherapy: A randomized, double-blinded, multi-center, phase III studyopen access
- Authors
- Lee, Seung-Ah; Lee, Cheol Whan; Park, Hwan-Cheol; Hong, Soon Jun; Sung, Jung-Hoon; Kim, Kyung-Soo; Kim, Seong Hwan; Cho, Jin Man; Chun, Sung Wan; Lee, Sang Rok; Kim, Chul Sik; Kim, Tae Nyun; Kim, Dae Hyeok; Kim, Byung Jin; Kim, Hyun-Sook; Choi, Ji-Yong; Hong, Young Joon; Chung, Joong Wha; Yoon, Seong Bo; Lee, Sang-Hak
- Issue Date
- Nov-2023
- Publisher
- Lippincott Williams & Wilkins Ltd.
- Keywords
- atorvastatin; cholesterol; ezetimibe; hypercholesterolemia; LDL
- Citation
- Medicine, v.102, no.47, pp 1 - 6
- Pages
- 6
- Indexed
- SCIE
SCOPUS
- Journal Title
- Medicine
- Volume
- 102
- Number
- 47
- Start Page
- 1
- End Page
- 6
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/193235
- DOI
- 10.1097/MD.0000000000036122
- ISSN
- 0025-7974
1536-5964
- Abstract
- Background: We compared the efficacy and safety of low-intensity atorvastatin and ezetimibe combination therapy with moderate-intensity atorvastatin monotherapy in patients requiring cholesterol-lowering therapy. Methods: At 19 centers in Korea, 290 patients were randomized to 4 groups: atorvastatin 5 mg and ezetimibe 10 mg (A5E), ezetimibe 10 mg (E), atorvastatin 5 mg (A5), and atorvastatin 10 mg (A10). Clinical and laboratory examinations were performed at baseline, and at 4-week and 8-week follow-ups. The primary endpoint was percentage change from baseline in low-density lipoprotein (LDL) cholesterol levels at the 8-week follow-up. Secondary endpoints included percentage changes from baseline in additional lipid parameters. Results: Baseline characteristics were similar among the study groups. At the 8-week follow-up, percentage changes in LDL cholesterol levels were significantly greater in the A5E group (49.2%) than in the E (18.7%), A5 (27.9%), and A10 (36.4%) groups. Similar findings were observed regarding the percentage changes in total cholesterol, non-high-density lipoprotein cholesterol, and apolipoprotein B levels. Triglyceride levels were also significantly decreased in the A5E group than in the E group, whereas high-density lipoprotein levels substantially increased in the A5E group than in the E group. In patients with low- and intermediate-cardiovascular risk, 93.3% achieved the target LDL cholesterol levels in the A5E group, 40.0% in the E group, 66.7% in the A5 group, and 92.9% in the A10 group. In addition, 31.4% of patients in the A5E group, 8.1% in E, 9.7% in A5, and 7.3% in the A10 group reached the target levels of both LDL cholesterol < 70 mg/dL and reduction of LDL ≥ 50% from baseline. Conclusions: The addition of ezetimibe to low-intensity atorvastatin had a greater effect on lowering LDL cholesterol than moderate-intensity atorvastatin alone, offering an effective treatment option for cholesterol management, especially in patients with low and intermediate risks.Abbreviations: A10 = atorvastatin 10 mg, A5 = atorvastatin 5 mg, A5E = atorvastatin 5mg and ezetimibe 10 mg, ASCVD = atherosclerotic cardiovascular disease, E = ezetimibe 10 mg, HDL = high-density lipoprotein, LDL = low-density lipoprotein.
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