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
[31]   PIOGLITAZONE ATTENUATES HYPERTENSION AND INHIBITS GROWTH OF RENAL ARTERIOLAR SMOOTH-MUSCLE IN RATS [J].
DUBEY, RK ;
ZHANG, HY ;
REDDY, SR ;
BOEGEHOLD, MA ;
KOTCHEN, TA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (04) :R726-R732
[32]   The metabolic syndrome [J].
Eckel, RH ;
Grundy, SM ;
Zimmet, PZ .
LANCET, 2005, 365 (9468) :1415-1428
[33]   An update on aspirin in the primary prevention of cardiovascular disease [J].
Eidelman, RS ;
Hebert, PR ;
Weisman, SM ;
Hennekens, CH .
ARCHIVES OF INTERNAL MEDICINE, 2003, 163 (17) :2006-2010
[34]   PPARs and the complex journey to obesity [J].
Evans, RM ;
Barish, GD ;
Wang, YX .
NATURE MEDICINE, 2004, 10 (04) :355-361
[35]  
Expert Committee on the Diagnosis and Classification of Diabetes Mellitus, 2003, Diabetes Care, V26, P5, DOI [10.2337/diacare.26.2007.s5, DOI 10.2337/DIACARE.26.2007.S5]
[36]   Peroxisome proliferator-activated receptor-γ:: from adipogenesis to carcinogenesis [J].
Fajas, L ;
Debril, MB ;
Auwerx, J .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2001, 27 (01) :1-9
[37]   Increasing prevalance of the metabolic syndrome among U.S adults [J].
Ford, ES ;
Giles, WH ;
Mokdad, AH .
DIABETES CARE, 2004, 27 (10) :2444-2449
[38]   Peroxisome proliferator-activated receptor-alpha activators regulate genes governing lipoprotein metabolism, vascular inflammation and atherosclerosis [J].
Fruchart, JC ;
Duriez, P ;
Staels, B .
CURRENT OPINION IN LIPIDOLOGY, 1999, 10 (03) :245-257
[39]   Regulation of lipid and lipoprotein metabolism by PPAR activators [J].
Gervois, P ;
Torra, IP ;
Fruchart, JC ;
Staels, B .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2000, 38 (01) :3-11
[40]   The metabolic syndrome and risk of major coronary events in the Scandinavian simvastatin survival study (4S) and the Air Force/Texas Coronary Atherosclerosis Prevention Study (AFCAPS/TexCAPS) [J].
Girman, CJ ;
Rhodes, T ;
Mercuri, M ;
Pyörälä, K ;
Kjekshus, J ;
Pedersen, TR ;
Beere, PA ;
Gotto, AM ;
Clearfield, M .
AMERICAN JOURNAL OF CARDIOLOGY, 2004, 93 (02) :136-141