Hypolipidemic therapy for the metabolic syndrome

被引:35
作者
Cignarella, Andrea
Bellosta, Stefano
Corsini, Alberto
Bolego, Chiara
机构
[1] Univ Milan, Dept Pharmacol Sci, I-20133 Milan, Italy
[2] Univ Padua, Dept Pharmacol & Anaesthesiol, I-35121 Padua, Italy
关键词
atherogenic dyslipidemia; lipid-lowering agents; cardiovascular disease; statins; fibrates;
D O I
10.1016/j.phrs.2006.03.012
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The metabolic syndrome appears to affect a significant proportion of the population and is associated with increased risk for development of cardiovascular disease as well as of type-2 diabetes. No single treatment for the metabolic syndrome as a whole yet exists. While the primary management of patients with the metabolic syndrome involves healthy lifestyle promotion, the atherogenic dyslipidemia is a primary target for cardiovascular disease risk reduction in these patients. Statin therapy provides effective reduction of LDL-cholesterol, which represents the primary therapeutic goal of lipid-lowering therapy in patients at risk for cardiovascular disease. Fibrates in turn are effective in normalizing lipid levels (mainly triglycerides and HDL-cholesterol) in patients with the metabolic syndrome and may improve insulin resistance. Whereas statins remain the drug of choice for patients who need to achieve the LDL-cholesterol goal, fibrate therapy may represent an alternative for those with low HDL-cholesterol and high triglyceride levels. The simultaneous use of fibrates could be indicated in patients whose LDL-cholesterol is controlled by statin therapy but whose HDL-cholesterol and/or triglycerides are still inappropriate. Such a combination, however, needs careful monitoring due to the potential hazard of adverse drug interactions. Nicotinic acid and ezetimibe may be useful agents for therapy, particularly when combined with statins. A number of emerging therapies offer potential as future options for the pharmacological treatment of metabolic syndrome. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:492 / 500
页数:9
相关论文
共 79 条
[1]
Effect of statin therapy on C-reactive protein levels - The Pravastatin Inflammation/CRP Evaluation (PRINCE): A randomized trial and cohort study [J].
Albert, MA ;
Danielson, E ;
Rifai, N ;
Ridker, PM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (01) :64-70
[2]
Treatment with atorvastatin to the National Cholesterol Educational Program goal versus 'usual' care in secondary coronary heart disease prevention - The GREek Atorvastatin and Coronary-heart-disease Evaluation (GREACE) Study [J].
Athyros, VG ;
Papageorgiou, AA ;
Mercouris, BR ;
Athyrou, VV ;
Symeonidis, AN ;
Basayannis, EO ;
Demitriadis, DS ;
Kontopoulos, AG .
CURRENT MEDICAL RESEARCH AND OPINION, 2002, 18 (04) :220-228
[3]
Targeting vascular risk in patients with metabolic syndrome but without diabetes [J].
Athyros, VG ;
Mikhailidis, DP ;
Papageorgiou, AA ;
Didangelos, TP ;
Peletidou, A ;
Kleta, D ;
Karagiannis, A ;
Kakafika, AI ;
Tziomalos, K ;
Elisaf, M .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2005, 54 (08) :1065-1074
[4]
Statin-fibrate combinations in patients with combined hyperlipidemia [J].
Athyros, VG ;
Papageorgiou, AA ;
Kontopoulos, AC .
ATHEROSCLEROSIS, 2001, 155 (01) :263-264
[5]
Influence of low high-density lipoprotein cholesterol and elevated triglyceride on coronary heart disease events and response to simvastatin therapy in 4S [J].
Ballantyne, CM ;
Olsson, AG ;
Cook, TJ ;
Mercuri, MF ;
Pedersen, TR ;
Kjekshus, J .
CIRCULATION, 2001, 104 (25) :3046-3051
[6]
Efficacy of rosuvastatin 10 mg in patients with the metabolic syndrome [J].
Ballantyne, CM ;
Stein, EA ;
Paoletti, R ;
Southworth, H ;
Blasetto, JW .
AMERICAN JOURNAL OF CARDIOLOGY, 2003, 91 (5A) :25C-27C
[7]
Pharmacotherapy for dyslipidaemia - current therapies and future agents [J].
Bays, H ;
Stein, EA .
EXPERT OPINION ON PHARMACOTHERAPY, 2003, 4 (11) :1901-1938
[8]
Bellosta S, 2000, DIABETES CARE, V23, pB72
[9]
Identification of telmisartan as a unique angiotensin II receptor antagonist with selective PPARγ-modulating activity [J].
Benson, SC ;
Pershadsingh, HA ;
Ho, CI ;
Chittiboyina, A ;
Desai, P ;
Pravenec, M ;
Qi, NN ;
Wang, JM ;
Avery, MA ;
Kurtz, TW .
HYPERTENSION, 2004, 43 (05) :993-1002
[10]
PPARs: therapeutic targets for metabolic disease [J].
Berger, JP ;
Akiyama, TE ;
Meinke, PT .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2005, 26 (05) :244-251