Thiazolidinediones and the Promise of Insulin Sensitization in Type 2 Diabetes

被引:416
作者
Soccio, Raymond E. [1 ,2 ]
Chen, Eric R. [1 ,2 ]
Lazar, Mitchell A. [1 ,2 ]
机构
[1] Univ Penn, Dept Med, Perelman Sch Med, Div Endocrinol Diabet & Metab,Dept Genet, Philadelphia, PA 19104 USA
[2] Univ Penn, Inst Diabet Obes & Metab, Perelman Sch Med, Philadelphia, PA 19104 USA
关键词
ACTIVATED-RECEPTOR-GAMMA; RANDOMIZED CONTROLLED-TRIAL; PIOGLITAZONE CLINICAL-TRIAL; CARDIOVASCULAR RISK-FACTORS; IMPAIRED GLUCOSE-TOLERANCE; CONGESTIVE-HEART-FAILURE; FATTY LIVER-DISEASE; ALL-CAUSE MORTALITY; PPAR-GAMMA; BLADDER-CANCER;
D O I
10.1016/j.cmet.2014.08.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Type 2 diabetes is caused by insulin resistance coupled with an inability to produce enough insulin to control blood glucose, and thiazolidinediones (TZDs) are the only current antidiabetic agents that function primarily by increasing insulin sensitivity. However, despite clear benefits in glycemic control, this class of drugs has recently fallen into disuse due to concerns over side effects and adverse events. Here we review the clinical data and attempt to balance the benefits and risks of TZD therapy. We also examine potential mechanisms of action for the beneficial and harmful effects of TZDs, mainly via agonism of the nuclear receptor PPARg. Based on critical appraisal of both preclinical and clinical studies, we discuss the prospect of harnessing the insulin sensitizing effects of PPARg for more effective, safe, and potentially personalized treatments of type 2 diabetes.
引用
收藏
页码:573 / 591
页数:19
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