Optimal lipid modification: the rationale for combination therapy

被引:21
作者
Backes, James [1 ]
Gibson, Cheryl [2 ]
Howard, Patricia [3 ]
机构
[1] Univ Kansas Med Ctr, Lipid Atherosclerosis Metab & LDL Apheresis Ctr, Dept Pharm Practice, Kansas City, KS 66160 USA
[2] Univ Kansas Med Ctr, Dept Internal Med, Kansas City, KS USA
[3] Univ Kansas Sch Pharm, Dept Pharm Practice, Kansas City, KS USA
关键词
combination therapy; coronary heart disease; hypercholesterolemia; lipid-lowering; low-density lipoprotein; statins;
D O I
10.2147/vhrm.2005.1.4.317
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Background: An emphasis on more aggressive lipid-lowering, particularly of low-density lipoprotein cholesterol, to improve patient outcomes has led to an increased use of combination lipid-lowering drugs. This strategy, while potentially beneficial, has triggered concerns regarding fears of adverse effects, harmful drug interactions, and patient nonadherence. Objective: To present key data regarding combination lipid-altering therapy including use, rationale, major trials, benefits, potential adverse effects, compliance issues, and limitations. Method: Literature was obtained from MEDLINE (1966 June 2005) and references from selected articles. Results: A substantial body of evidence from epidemiological data and clinical trials indicates that aggressive lipid modification, especially low-density lipoprotein reduction, is associated with reduced cardiovascular events. Numerous studies utilizing various combinations of cholesterol-lowering agents including statin/fibrate, statin/niacin, statin/bile acid resin, and statin/ezetimibe have demonstrated significant changes in the lipid profile with acceptable safety. Long-term trials of combination therapy evaluating clinical outcomes or surrogate markers of cardiovascular disease, while limited, are promising. Conclusion: Combining lipid-altering agents results in additional improvements in lipoproteins and has the potential to further reduce cardiovascular events beyond that of monotherapy.
引用
收藏
页码:317 / 331
页数:15
相关论文
共 141 条
[1]   Colesevelam hydrochloride: A novel bile acid-binding resin [J].
Aldridge, MA ;
Ito, MK .
ANNALS OF PHARMACOTHERAPY, 2001, 35 (7-8) :898-907
[2]   INFLUENCE OF NICOTINIC ACID ON SERUM CHOLESTEROL IN MAN [J].
ALTSCHUL, R ;
HOFFER, A ;
STEPHEN, JD .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1955, 54 (02) :558-559
[3]   DISCONTINUATION OF ANTIHYPERLIPIDEMIC DRUGS - DO RATES REPORTED IN CLINICAL-TRIALS REFLECT RATES IN PRIMARY-CARE SETTINGS [J].
ANDRADE, SE ;
WALKER, AM ;
GOTTLIEB, LK ;
HOLLENBERG, NK ;
TESTA, MA ;
SAPERIA, GM ;
PLATT, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (17) :1125-1131
[4]  
[Anonymous], 1975, JAMA-J AM MED ASSOC, V231, P360
[5]  
[Anonymous], HEART DIS STROK STAT
[6]   EFFECTS OF LOVASTATIN THERAPY ON VERY-LOW-DENSITY LIPOPROTEIN TRIGLYCERIDE-METABOLISM IN SUBJECTS WITH COMBINED HYPERLIPIDEMIA - EVIDENCE FOR REDUCED ASSEMBLY AND SECRETION OF TRIGLYCERIDE-RICH LIPOPROTEINS [J].
ARAD, Y ;
RAMAKRISHNAN, R ;
GINSBERG, HN .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1992, 41 (05) :487-493
[7]   Atorvastatin improves endothelial function in renal-transplant recipients [J].
Åsberg, A ;
Hartmann, A ;
Fjeldså, E ;
Holdaas, H .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2001, 16 (09) :1920-1924
[8]   Atorvastatin and micronized fenofibrate alone and in combination in type 2 diabetes with combined hyperlipidemia [J].
Athyros, VG ;
Papageorgiou, AA ;
Athyrou, VV ;
Demitriadis, DS ;
Kontopoulos, AG .
DIABETES CARE, 2002, 25 (07) :1198-1202
[9]   Safety and efficacy of long-term statin-fibrate combinations in patients with refractory familial combined hyperlipidemia [J].
Athyros, VG ;
Papageorgiou, AA ;
Hatzikonstandinou, HA ;
Didangelos, TP ;
Carina, MV ;
Kranitsas, DF ;
Kontopoulos, AG .
AMERICAN JOURNAL OF CARDIOLOGY, 1997, 80 (05) :608-613
[10]   Effect of lipid-lowering drug therapy on small-dense low-density lipoprotein [J].
Backes, JM ;
Gibson, CA .
ANNALS OF PHARMACOTHERAPY, 2005, 39 (03) :523-526