Drug therapy of the metabolic syndrome: minimizing the emerging crisis in polypharmacy

被引:215
作者
Grundy, SM
机构
[1] Univ Texas, SW Med Ctr, Ctr Human Nutr, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Clin Nutr, Dallas, TX 75390 USA
[3] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75390 USA
关键词
D O I
10.1038/nrd2005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The metabolic syndrome-a collection of factors associated with increased risk for cardiovascular disease and diabetes-is becoming increasingly common, largely as a result of the increase in the prevalence of obesity. Although it is generally agreed that first-line clinical intervention for the metabolic syndrome is lifestyle change, this is insufficient to normalize the risk factors in many patients, and so residual risk could be high enough to justify drug therapy. However, at present there are no approved drugs that can reliably reduce all of the metabolic risk factors over the long term, and so there is growing interest in therapeutic strategies that might target multiple risk factors more effectively, thereby minimizing problems with polypharmacy. This review summarizes current understanding of the nature of the metabolic syndrome, and discusses each of the risk factors of the metabolic syndrome as possible primary drug targets; potential secondary or tertiary targets are also considered.
引用
收藏
页码:294 / 309
页数:15
相关论文
共 129 条
  • [1] Insulin sensitivity at diagnosis of Type 2 diabetes is not associated with subsequent cardiovascular disease (UKPDS 67)
    Adler, AI
    Levy, JC
    Matthews, DR
    Stratton, IM
    Hines, G
    Holman, RR
    [J]. DIABETIC MEDICINE, 2005, 22 (03) : 306 - 311
  • [2] NCEP-defined metabolic syndrome, diabetes, and prevalence of coronary heart disease among NHANES III participants age 50 years and older
    Alexander, CM
    Landsman, PB
    Teutsch, SM
    Haffner, SM
    [J]. DIABETES, 2003, 52 (05) : 1210 - 1214
  • [3] ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group, 2002, JAMA-J AM MED ASSOC, V288, P2981
  • [4] The efficacy and safety of sibutramine for weight loss - A systematic review
    Arterburn, DE
    Crane, PK
    Veenstra, DL
    [J]. ARCHIVES OF INTERNAL MEDICINE, 2004, 164 (09) : 994 - 1003
  • [5] Baigent C, 2002, BMJ-BRIT MED J, V324, P71, DOI 10.1136/bmj.324.7329.71
  • [6] Metabolic effects of carvedilol vs metoprolol in patients with type 2 diabetes mellitus and hypertension - A randomized controlled trial
    Bakris, GL
    Fonseca, V
    Katholi, RE
    McGill, JB
    Messerli, FH
    Phillips, RA
    Raskin, P
    Wright, JT
    Oakes, R
    Lukas, MA
    Anderson, KM
    Bell, DSH
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 292 (18): : 2227 - 2236
  • [7] Prevention and Rehabilitation - Dose-comparison study of the combination of ezetimibe and simvastatin (Vytorin) versus atorvastatin in patients with hypercholesterolemia: The Vytorin Versus Atorvastatin (VYVA) Study
    Ballantyne, CM
    Abate, N
    Yuan, Z
    King, TR
    Palmisano, J
    [J]. AMERICAN HEART JOURNAL, 2005, 149 (03) : 464 - 473
  • [8] Effects of peroxisome proliferator-activated receptor δ on placentation, adiposity, and colorectal cancer
    Barak, Y
    Liao, D
    He, WM
    Ong, ES
    Nelson, MC
    Olefsky, JM
    Boland, R
    Evans, RM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) : 303 - 308
  • [9] Pharmacotherapy for dyslipidaemia - current therapies and future agents
    Bays, H
    Stein, EA
    [J]. EXPERT OPINION ON PHARMACOTHERAPY, 2003, 4 (11) : 1901 - 1938
  • [10] Comparison of once-daily, niacin extended/release/lovastatin with standard doses of atorvastatin and simvastafin (The Advicor Versus Other Cholesterol-Modulating Agents Trial Evaluation [ADVOCATE])
    Bays, HE
    Dujovne, CA
    McGovern, ME
    White, TE
    Kashyap, ML
    Hutcheson, AG
    Crouse, JR
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2003, 91 (06) : 667 - 672