Effect of plasminogen activator inhibitor-1 in diabetes mellitus and cardiovascular disease

被引:108
作者
Lyon, CJ [1 ]
Hsueh, WA [1 ]
机构
[1] Univ Calif Los Angeles, Div Endocrinol Diabet & Hypertens, Los Angeles, CA 90095 USA
关键词
D O I
10.1016/j.amjmed.2003.08.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Concentrations of plasminogen activator inhibitor-1 (PAI-1) are elevated beginning at the stage of impaired glucose tolerance and continuing through the development of diabetes mellitus and the metabolic syndrome. Evolving evidence of the central role of PAI-1 in mediating fibrosis and thrombosis increasingly supports the theory that it is a significant risk factor for macrovascular complications and cardiovascular disease, particularly in patients with diabetes. Several clinical studies have demonstrated a strong correlation between circulating PAI-1 levels and cardiovascular events and mortality. With the potentially severe effects of elevated PAI-1 levels becoming evident, there is increased interest in developing therapies targeted at reducing PAI-1 expression or circulating concentrations. Thus far, weight loss, inhibitors of the renin-angiotensin system, and insulin sensitization through use of thiazolidinediones (TZDs) appear to be the most promising strategies for managing elevated PAI-1 levels. Of these, TZD therapy is the only one that provides the benefits of both long-term glycemic control and improved cardiovascular risk profile. This article reviews the regulation of PAI-1, its activity in various disease states, and available treatment options. (C) 2003 by Excerpta Medica, Inc.
引用
收藏
页码:62 / 68
页数:7
相关论文
共 93 条
[61]   Differential regulation by troglitazone of plasminogen activator inhibitor type 1 in human hepatic and vascular cells [J].
Nordt, TK ;
Peter, K ;
Bode, C ;
Sobel, BE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (04) :1563-1568
[62]   PAI-1 deficiency attenuates the fibrogenic response to ureteral obstruction [J].
Oda, T ;
Jung, YO ;
Kim, HS ;
Cai, XH ;
López-Guisa, JM ;
Ikeda, Y ;
Eddy, AA .
KIDNEY INTERNATIONAL, 2001, 60 (02) :587-596
[63]   Platelet-activating factor induces the gene expression of TIMP-1,-2, and PAI-1: Imbalance between the gene expression of MMP-9 and TIMP-1 and-2 [J].
Ottino, P ;
Taheri, F ;
Bazan, HEP .
EXPERIMENTAL EYE RESEARCH, 2002, 74 (03) :393-402
[64]   Effect of glucose tolerance status on PAI-1 plasma levels in overweight and obese subjects [J].
Pannacciulli, N ;
De Mitrio, V ;
Marino, R ;
Giorgino, R ;
De Pergola, G .
OBESITY RESEARCH, 2002, 10 (08) :717-725
[65]   TRANSFORMING GROWTH FACTOR-BETA-1 MODULATES BASIC FIBROBLAST GROWTH-FACTOR INDUCED PROTEOLYTIC AND ANGIOGENIC PROPERTIES OF ENDOTHELIAL-CELLS INVITRO [J].
PEPPER, MS ;
BELIN, D ;
MONTESANO, R ;
ORCI, L ;
VASSALLI, JD .
JOURNAL OF CELL BIOLOGY, 1990, 111 (02) :743-755
[66]   CELL-SPECIFIC REGULATION OF PLASMINOGEN-ACTIVATOR INHIBITOR-1 AND TISSUE-TYPE PLASMINOGEN-ACTIVATOR RELEASE BY HUMAN KIDNEY MESANGIAL CELLS [J].
PERALDI, MN ;
RONDEAU, E ;
MEDCALF, RL ;
HAGEGE, J ;
LACAVE, R ;
DELARUE, F ;
SCHLEUNING, WD ;
SRAER, JD .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1134 (03) :189-196
[67]   NIDDM as a disease of the innate immune system: association of acute-phase reactants and interleukin-6 with metabolic syndrome X [J].
Pickup, JC ;
Mattock, MB ;
Chusney, GD ;
Burt, D .
DIABETOLOGIA, 1997, 40 (11) :1286-1292
[68]  
PRIMROSE JN, 1992, THROMB HAEMOSTASIS, V68, P396
[69]   NITRIC-OXIDE ACTIVITY IN THE HUMAN CORONARY CIRCULATION - IMPACT OF RISK-FACTORS FOR CORONARY ATHEROSCLEROSIS [J].
QUYYUMI, AA ;
DAKAK, N ;
ANDREWS, NP ;
HUSAIN, S ;
ARORA, S ;
GILLIGAN, DM ;
PANZA, JA ;
CANNON, RO .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (04) :1747-1755
[70]  
REILLY CF, 1991, J BIOL CHEM, V266, P9419