A randomized, open-label, parallel, multi-center Phase IV study to compare the efficacy and safety of atorvastatin 10 and 20 mg in high-risk Asian patients with hypercholesterolemia

被引:5
作者
Kim, Ji Bak [1 ]
Song, Woo Hyuk [2 ]
Park, Jong Sung [3 ]
Youn, Tae-Jin [4 ,5 ]
Park, Yong Hyun [6 ]
Kim, Shin-Jae [7 ]
Ahn, Sung Gyun [8 ]
Doh, Joon-Hyung [9 ]
Cho, Yun-Hyeong [10 ]
Kim, Jin Won [11 ]
机构
[1] Korea Univ, Dept Med, Grad Sch, Seoul, South Korea
[2] Korea Univ, Dept Internal Med, Div Cardiol, Ansan Hosp, Ansan, South Korea
[3] Dong A Univ Hosp, Dept Cardiol, Busan, South Korea
[4] Seoul Natl Univ, Div Cardiol, Coll Med, Dept Internal Med, Seongnam, South Korea
[5] Seoul Natl Univ, Cardiovasc Ctr, Bundang Hosp, Seongnam, South Korea
[6] Pusan Natl Univ, Cardiovasc Ctr, Dept Internal Med, Div Cardiol,Yangsan Hosp, Yangsan, South Korea
[7] Univ Ulsan, Ulsan Univ Hosp, Dept Cardiol, Coll Med, Ulsan, South Korea
[8] Wonju Severance Christian Hosp, Dept Internal Med, Div Cardiol, Wonju, South Korea
[9] Inje Univ, Dept Cardiol, Ilsan Paik Hosp, Goyang, South Korea
[10] Myongji Hosp, Dept Internal Med, Goyang, South Korea
[11] Korea Univ, Cardiovasc Ctr, Guro Hosp, Seoul, South Korea
来源
PLOS ONE | 2021年 / 16卷 / 01期
关键词
CARDIOVASCULAR RISK; CHOLESTEROL; THERAPY; DISCONTINUATION; DYSLIPIDEMIA; PREVENTION; ADHERENCE; STATINS;
D O I
10.1371/journal.pone.0245481
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Although accumulating evidence suggests a more extensive reduction of low-density lipoprotein cholesterol (LDL-C), it is unclear whether a higher statin dose is more effective and cost-effective in the Asian population. This study compared the efficacy, safety, and cost-effectiveness of atorvastatin 20 and 10 mg in high-risk Asian patients with hypercholesterolemia. Methods A 12-week, open-label, parallel, multicenter, Phase IV randomized controlled trial was conducted at ten hospitals in the Republic of Korea between October 2017 and May 2019. High-risk patients with hypercholesterolemia, defined according to 2015 Korean guidelines for dyslipidemia management, were eligible to participate. We randomly assigned 250 patients at risk of atherosclerotic cardiovascular disease to receive 20 mg (n = 124) or 10 mg (n = 126) of atorvastatin. The primary endpoint was the difference in the mean percentage change in LDL-C levels from baseline after 12 weeks. Cost-effectiveness was measured as an exploratory endpoint. Results LDL-C levels were reduced more significantly by atorvastatin 20 mg than by 10 mg after 12 weeks (42.4% vs. 33.5%, p < 0.0001). Significantly more patients achieved target LDL-C levels (<100 mg/dL for high-risk patients, <70 mg/dL for very high-risk patients) with atorvastatin 20 mg than with 10 mg (40.3% vs. 25.6%, p < 0.05). Apolipoprotein B decreased significantly with atorvastatin 20mg versus 10 mg (-36.2% vs. -29.9%, p < 0.05). Lipid ratios also showed greater improvement with atorvastatin 20 mg than with 10 mg (total cholesterol/high-density lipoprotein cholesterol ratio, -33.3% vs. -29.4%, p < 0.05; apolipoprotein B/apolipoprotein A1 ratio, -36.7% vs. -31.4%, p < 0.05). Atorvastatin 20 mg was more cost-effective than atorvastatin 10 mg in terms of both the average and incremental cost-effectiveness ratios. Safety and tolerability of atorvastatin 20 mg were comparable to those of atorvastatin 10 mg. Conclusion In high-risk Asian patients with hypercholesterolemia, atorvastatin 20 mg was both efficacious in reducing LDL-C and cost-effective compared with atorvastatin 10 mg.
引用
收藏
页数:17
相关论文
共 42 条
[1]   Sub-optimal cholesterol response to initiation of statins and future risk of cardiovascular disease [J].
Akyea, Ralph Kwame ;
Kai, Joe ;
Qureshi, Nadeem ;
Iyen, Barbara ;
Weng, Stephen F. .
HEART, 2019, 105 (13) :975-+
[2]  
Arnett DK, 2019, CIRCULATION, V140, pE563, DOI [10.1161/CIR.0000000000000678, 10.1161/CIR.0000000000000677, 10.1016/j.jacc.2019.03.009, 10.1016/j.jacc.2019.03.010]
[3]   Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170 000 participants in 26 randomised trials [J].
Baigent, C. ;
Blackwell, L. ;
Emberson, J. ;
Holland, L. E. ;
Reith, C. ;
Bhala, N. ;
Peto, R. ;
Barnes, E. H. ;
Keech, A. ;
Simes, J. ;
Collins, R. .
LANCET, 2010, 376 (9753) :1670-1681
[4]  
Baigent C., 2010, Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170
[5]  
Bittencourt MS, 2019, STATIN DOSE PRIMARY
[6]   Trends in statin prescription prevalence, initiation, and dosing: Hong Kong, 2004-2015 [J].
Blais, Joseph E. ;
Chan, Esther W. ;
Law, Sharon W. Y. ;
Mok, Michael T. ;
Huang, Duo ;
Wong, Ian C. K. ;
Siu, Chung-Wah .
ATHEROSCLEROSIS, 2019, 280 :174-182
[7]   Mevalonate pathway: A review of clinical and therapeutical implications [J].
Buhaescu, Irina ;
Izzedine, Hassane .
CLINICAL BIOCHEMISTRY, 2007, 40 (9-10) :575-584
[8]   Intensive versus moderate lipid lowering with statins after acute coronary syndromes [J].
Cannon, CP ;
Braunwald, E ;
McCabe, CH ;
Rader, DJ ;
Rouleau, JL ;
Belder, R ;
Joyal, SV ;
Hill, KA ;
Pfeffer, MA ;
Skene, AM .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (15) :1495-1504
[9]   Safety of atorvastatin in Asian patients within clinical trials [J].
Chan, Juliana C. N. ;
Kong, Alice P. S. ;
Bao, Weihang ;
Fayyad, Rana ;
Laskey, Rachel .
CARDIOVASCULAR THERAPEUTICS, 2016, 34 (06) :431-440
[10]   Dyslipidemia management update [J].
Chang, Yingzi ;
Robidoux, Jacques .
CURRENT OPINION IN PHARMACOLOGY, 2017, 33 :47-55