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
[81]   The Metabolic Syndrome is associated with advanced vascular damage in patients with coronary heart disease, stroke, peripheral arterial disease or abdominal aortic aneurysm [J].
Olijhoek, JK ;
van der Graaf, Y ;
Banga, JD ;
Algra, A ;
Rabelink, TJ ;
Visseren, FLJ .
EUROPEAN HEART JOURNAL, 2004, 25 (04) :342-348
[82]   A selective peroxisome proliferator-activated receptor δ agonist promotes reverse cholesterol transport [J].
Oliver, WR ;
Shenk, JL ;
Snaith, MR ;
Russell, CS ;
Plunket, KD ;
Bodkin, NL ;
Lewis, MC ;
Winegar, DA ;
Sznaidman, ML ;
Lambert, MH ;
Xu, HE ;
Sternbach, DD ;
Kliewer, SA ;
Hansen, BC ;
Willson, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (09) :5306-5311
[83]   Endocannabinoid activation at hepatic CB1 receptors stimulates fatty acid synthesis and contributes to diet-induced obesity [J].
Osei-Hyiaman, D ;
DePetrillo, M ;
Pacher, P ;
Liu, J ;
Radaeva, S ;
Bátkai, S ;
Harvey-White, J ;
Mackie, K ;
Offertáler, L ;
Wang, L ;
Kunos, G .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (05) :1298-1305
[84]   Effects of diet and exercise in preventing NIDDM in people with impaired glucose tolerance - The Da Qing IGT and diabetes study [J].
Pan, XR ;
Li, GW ;
Hu, YH ;
Wang, JX ;
Yang, WY ;
An, ZX ;
Hu, ZX ;
Lin, J ;
Xiao, JZ ;
Cao, HB ;
Liu, PA ;
Jiang, XG ;
Jiang, YY ;
Wang, JP ;
Zheng, H ;
Zhang, H ;
Bennett, PH ;
Howard, BV .
DIABETES CARE, 1997, 20 (04) :537-544
[85]   Metabolic syndrome without obesity:: Hepatic overexpression of 11β-hydroxysteroid dehydrogenase type 1 in transgenic mice [J].
Paterson, JM ;
Morton, NM ;
Fievet, C ;
Kenyon, CJ ;
Holmes, MC ;
Staels, B ;
Seckl, JR ;
Mullins, JJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (18) :7088-7093
[86]   A community-based, randomized trial of ezetimibe added to statin therapy to attain NCEP ATP III goals for LDL cholesterol in hypercholesterolemic patients: The ezetimibe add-on to statin for effectiveness (EASE) trial [J].
Pearson, TA ;
Denke, MA ;
McBride, PE ;
Battisti, WP ;
Brady, WE ;
Palmisano, J .
MAYO CLINIC PROCEEDINGS, 2005, 80 (05) :587-595
[87]   AHA guidelines for primary prevention of cardiovascular disease and stroke: 2002 update - Consensus panel guide to comprehensive risk reduction for adult patients without coronary or other atherosclerotic vascular diseases [J].
Pearson, TA ;
Blair, SN ;
Daniels, SR ;
Eckel, RH ;
Fair, JM ;
Fortmann, SP ;
Franklin, BA ;
Goldstein, LB ;
Greenland, P ;
Grundy, SM ;
Hong, YL ;
Miller, NH ;
Lauer, RM ;
Ockene, IS ;
Sacco, RL ;
Sallis, JF ;
Smith, SC ;
Stone, NJ ;
Taubert, KA .
CIRCULATION, 2002, 106 (03) :388-391
[88]   Growth, adipose, brain, and skin alterations resulting from targeted disruption of the mouse peroxisome proliferator-activated receptor β(δ) [J].
Peters, JM ;
Lee, SST ;
Li, W ;
Ward, JM ;
Gavrilova, O ;
Everett, C ;
Reitman, ML ;
Hudson, LD ;
Gonzalez, FJ .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (14) :5119-5128
[89]  
Pi-Sunyer FX, 1998, OBES RES, V6, p51S
[90]  
POLLARE T, 1989, BMJ-BRIT MED J, V248, P115