Statin-fibrate combination therapy for hyperlipidaemia: a review

被引:136
作者
Wierzbicki, AS
Mikhailidis, DP
Wray, R
Schachter, M
Cramb, R
Simpson, WG
Byrne, CB
机构
[1] St Thomas Hosp, Dept Chem Pathol, London SE1 7EH, England
[2] Royal Free Hosp, Dept Clin Biochem, London NW3 2QG, England
[3] Conquest Hosp, Dept Cardiol, St Leonards On Sea TN37 7RD, E Sussex, England
[4] St Marys Hosp, Dept Clin Pharmacol, London W2, England
[5] Queen Elizabeth II Hosp, Dept Chem Pathol, Birmingham, W Midlands, England
[6] Aberdeen Royal Infirm, Dept Clin Biochem, Aberdeen, Scotland
[7] Southampton Hosp, Dept Diabet & Metab, Southampton, Hants, England
关键词
combination therapy; fibrate; HMG-CoA reductase inhibitor; review; statin;
D O I
10.1185/030079903125001668
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Statins and fibrates are well-established treatments for hyperlipidaemias and the prevention of vascular events. However, fibrate + statin therapy has been restricted following early reports of rhabdomyolysis that mainly involved gemfibrozil, originally with lovastatin, and recently, with cerivastatin. Despite this limitation, several reports describing combination therapy have been published. This review considers these studies and the relevant indications and contraindications. Stalin + fibrate therapy should be considered if monotherapy or adding other drugs (e.g. cholesterol absorption inhibitors, omega-3 fatty acids or nicotinic acid) did not achieve lipid targets or is impractical. Combination therapy should be hospital-based and reserved for high-risk patients with a mixed hyperlipidaemia characterised by low density lipoprotein cholesterol (LDL) >2.6mmol/I (100 mg/dl), high density lipoprotein cholesterol (HDL) < 1.0 mmol/l (40 mg/dl) and/or triglycerides > 5.6 mmol/l (500 mg/dl). These three 'goals' are individually mentioned in guidelines. Patients should have normal renal, liver and thyroid function tests and should not be receiving therapy with cyclosporine, protease inhibitors or drugs metabolised through cytochrome P-450 (especially W). Combination therapy is probably best conducted using drugs with short plasma half-lives; fibrates should be prescribed in the morning and statins at night to minimise peak dose interactions. Both drug classes should be progressively titrated from low doses. Regular (3-monthly) monitoring of liver function and creatine kinase is required. In conclusion, fibrate + statin therapy remains an option in high-risk patients. However, long-term studies involving safety monitoring and vascular endpoints are required to demonstrate the efficacy of this regimen.
引用
收藏
页码:155 / 168
页数:14
相关论文
共 133 条
[41]   INSULIN-RESISTANCE - SYNDROME OR TENDENCY [J].
GODSLAND, IF ;
STEVENSON, JC .
LANCET, 1995, 346 (8967) :100-103
[42]   Cardiovascular events and their reduction with pravastatin in diabetic and glucose-intolerant myocardial infarction survivors with average cholesterol levels -: Subgroup analyses in the cholesterol and recurrent events (CARE) trial [J].
Goldberg, RB ;
Mellies, MJ ;
Sacks, FM ;
Moyé, LA ;
Howard, BV ;
Howard, WJ ;
Davis, BR ;
Cole, TG ;
Pfeffer, MA ;
Braunwald, E .
CIRCULATION, 1998, 98 (23) :2513-2519
[43]   Relation between baseline and on-treatment lipid parameters and first acute major coronary events in the Air Force/Texas Coronary Atherosclerosis Prevention Study (AFCAPS/TexCAPS) [J].
Gotto, AM ;
Whitney, E ;
Stein, EA ;
Shapiro, DR ;
Clearfield, M ;
Weis, S ;
Jou, JY ;
Langendörfer, A ;
Beere, A ;
Watson, DJ ;
Downs, JR ;
de Cani, JS .
CIRCULATION, 2000, 101 (05) :477-484
[44]   High-density lipoprotein enhancement of anticoagulant activities of plasma protein S and activated protein C [J].
Griffin, JH ;
Kojima, K ;
Banka, CL ;
Curtiss, LK ;
Fernández, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (02) :219-227
[45]   Efficacy, safety, and tolerability of once-daily niacin for the treatment of dyslipidemia associated with type 2 diabetes - Results of the assessment of diabetes control and evaluation of the efficacy of niaspan trial [J].
Grundy, SM ;
Vega, GL ;
McGovern, ME ;
Tulloch, BR ;
Kendall, DM ;
Fitz-Patrick, D ;
Ganda, OP ;
Rosenson, RS ;
Buse, JB ;
Robertson, DD ;
Sheehan, JP .
ARCHIVES OF INTERNAL MEDICINE, 2002, 162 (14) :1568-1576
[46]   Small LDL, atherogenic dyslipidemia, and the metabolic syndrome [J].
Grundy, SM .
CIRCULATION, 1997, 95 (01) :1-4
[47]   Combination drug therapy for combined hyperlipidemia [J].
Guyton J.R. .
Current Cardiology Reports, 1999, 1 (3) :244-250
[48]   Mortality from coronary heart disease in subjects with type 2 diabetes and in nondiabetic subjects with and without prior myocardial infarction [J].
Haffner, SM ;
Lehto, S ;
Rönnemaa, T ;
Pyörälä, K ;
Laakso, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (04) :229-234
[49]  
HEADY JA, 1980, LANCET, V2, P379
[50]   Atorvastatin and gemfibrozil for protease-inhibitor-related lipid abnormalities [J].
Henry, K ;
Melroe, H ;
Huebesch, J ;
Hermundson, J ;
Simpson, J .
LANCET, 1998, 352 (9133) :1031-1032