Combination therapy of low-dose atorvastatin and fenofibrate in mixed hyperlipidemia

被引:3
|
作者
Chatley, P.
Badyal, D. K. [1 ]
Calton, R.
Khosla, P. P.
机构
[1] Christian Med Coll & Hosp, Dept Pharmacol, Ludhiana 141008, Punjab, India
[2] Christian Med Coll & Hosp, Dept Cardiol, Ludhiana 141008, Punjab, India
来源
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY | 2007年 / 29卷 / 03期
关键词
atorvastatin; combination; fenofibrate; hyperlipidemia;
D O I
10.1358/mf.2007.29.3.1075363
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mixed hyperlipidemia is a major cause of coronary artery disease. Monotherapy with statins is considered the gold standard for treatment of mixed hyperlipidemia. But greater benefit may be expected by combination therapy. Combination may allow lower doses of statins and less adverse effects. Hence, this preliminary study was designed to evaluate the efficacy and safety of low-dose atorvastatin in combination with fenofibrate in patients with mixed hyperlipidemia. Ninety patients were assigned into three groups and received atorvastatin (10-40 mg/day) or fenofibrate (160-200 mg/day) or combination of low-dose atorvastatin (5 mg/day) and fenofibrate (160 mg/day). There was a significant decrease in low-density lipoprotein (LDL), triglycerides (TG) and total cholesterol (TC), and a significant increase in high density lipoprotein (HDL) in all the groups at the end of therapy. Combination therapy produced maximum decrease in LDL, TG and TC, and maximum increase in HDL when compared with monotherapies. No significant difference was reported in safety profile between the two groups. To conclude, the results suggest that combination therapy with low-dose atorvastatin and fenofibrate is more efficacious, with no increase in adverse effects when compared with monotherapies with individual drugs for mixed hyperlipidemia. The results are preliminary and suggestive only, as the study was open and nonrandomized. (c) 2007 Prous Science. All rights reserved.
引用
收藏
页码:217 / 221
页数:5
相关论文
共 50 条
  • [31] Treatment With Low-dose Atorvastatin, Losartan, and Their Combination Increases Expression of Vasoactive-Related Genes in Rat Aortas
    Lunder, Mojca
    Drevensek, Gorazd
    Cerne, Darko
    Marc, Janja
    Janic, Miodrag
    Sabovic, Miso
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY AND THERAPEUTICS, 2013, 18 (02) : 177 - 183
  • [32] Efficacy and Tolerability of Atorvastatin/Fenofibrate Fixed-Dose Combination Tablet Compared With Atorvastatin and Fenofibrate Monotherapies in Patients With Dyslipidemia: A 12-Week, Multicenter, Double-Blind, Randomized, Parallel-Group Study
    Davidson, Michael H.
    Rooney, Michael W.
    Drucker, Joan
    Griffin, H. Eugene
    Oosman, Sonia
    Beckert, Michael
    CLINICAL THERAPEUTICS, 2009, 31 (12) : 2824 - 2838
  • [33] Impact of short-term low-dose atorvastatin on low-density lipoprotein and high-density lipoprotein subfraction phenotype
    Xu, Rui-Xia
    Guo, Yuan-Lin
    Li, Xiao-Lin
    Li, Sha
    Li, Jian-Jun
    CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2014, 41 (07) : 475 - 481
  • [34] A low-dose atorvastatin and losartan combination directly improves aortic ring relaxation and diminishes ischaemic-reperfusion injury in isolated rat hearts
    Lunder, Mojca
    Janic, Miodrag
    Ziberna, Lovro
    Drevensek, Gorazd
    Sabovic, Miso
    MEDICAL SCIENCE MONITOR, 2012, 18 (09): : BR366 - BR374
  • [35] Differential effects of low-dose fenofibrate treatment in diabetic rats with early onset nephropathy and established nephropathy
    Kadian, Supriya
    Mahadevan, Nanjaian
    Balakumar, Pitchai
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2013, 698 (1-3) : 388 - 396
  • [36] The "Rise-Peak-Fall" Pattern of Time Dependency of the Cardiovascular Pleiotropic Effects of Treatment With Low-dose Atorvastatin, Losartan, and a Combination Thereof in Rats
    Janic, Miodrag
    Lunder, Mojca
    Cerne, Darko
    Marc, Janja
    Jerin, Ales
    Skitek, Milan
    Drevensek, Gorazd
    Sabovic, Miso
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2016, 68 (01) : 74 - 80
  • [37] Combination therapy with fluvastatin and fenofibrate in ischemic heart disease patients with combined hyperlipidemia and type 2 diabetes
    Sarano, NE
    Kozlov, SG
    Tvorogova, MG
    Lyakishev, AA
    Naumov, VG
    KARDIOLOGIYA, 2003, 43 (04) : 30 - 35
  • [38] Efficacy and safety of a new hydroxymethylglutaryl-coenzyme a reductase inhibitor, atorvastatin, in patients with combined hyperlipidemia: Comparison with fenofibrate
    Ooi, TC
    Heinonen, T
    Alaupovic, P
    Davignon, J
    Leiter, L
    Lupien, PJ
    Sniderman, AD
    Tan, MH
    Tremblay, G
    Sorisky, A
    Shurzinske, L
    Black, DM
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (09) : 1793 - 1799
  • [39] EFFICACY AND SAFETY OF ADDING EZETIMIBE TO LOW-DOSE ATORVASTATIN FOR HIGHLY ACTIVE ANTIRETROVIRAL THERAPY-RELATED HYPERCHOLESTEROLAEMIA
    Palacios Munoz, Rosario
    Puerta Fernandez, Susana
    Hidalgo Conde, Ana
    Ruiz Morales, Josefa
    Gonzalez Serrano, Mercedes
    Marquez Solero, Manuel
    Santos Gonzalez, Jesus
    CLINICA E INVESTIGACION EN ARTERIOSCLEROSIS, 2009, 21 (04): : 185 - 189
  • [40] LOW-DOSE COMBINED THERAPY WITH FLUVASTATIN AND CHOLESTYRAMINE IN HYPERLIPIDEMIC PATIENTS
    SPRECHER, DL
    ABRAMS, J
    ALLEN, JW
    KEANE, WF
    CHRYSANT, SG
    GINSBERG, H
    FISCHER, JJ
    JOHNSON, BF
    THEROUX, P
    JOKUBAITIS, L
    ANNALS OF INTERNAL MEDICINE, 1994, 120 (07) : 537 - 543