Circulating tissue factor procoagulant activity and thrombin generation in patients with type 2 diabetes: Effects of insulin and glucose

被引:116
作者
Boden, Guenther
Vaidyula, Vijender R.
Homko, Carol
Cheung, Peter
Rao, A. Koneti
机构
[1] Temple Univ, Sch Med, Div Endocrinol Diabetes Metab, Philadelphia, PA 19140 USA
[2] Temple Univ, Sch Med, Clin Res Ctr, Div Hematol, Philadelphia, PA 19140 USA
[3] Temple Univ, Sch Med, Sol Thrombosis Res Ctr, Philadelphia, PA 19140 USA
关键词
D O I
10.1210/jc.2007-0933
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Type 2 diabetes mellitus ( T2DM) is a hypercoagulable state. Tissue factor ( TF) is the principal initiator of blood coagulation. Objective: Our objective was to examine the effects of hyperglycemia and hyperinsulinemia on the TF pathway of blood coagulation in T2DM. Design: Three study protocols were used: 1) acute correction of hyperglycemia ( with iv insulin) followed by 24 h of euglycemia, 2) 24 h of selective hyperinsulinemia, and 3) 24 h of combined hyperinsulinemia and hyperglycemia. Setting: The study took place at a clinical research center. Study Participants: Participants included 18 T2DM patients and 22 nondiabetic controls. Results: Basal TF-procoagulant activity ( TF-PCA), monocyte TF mRNA, plasma coagulation factor VII ( FVIIc), and thrombin-antithrombin complexes were higher in T2DM than in nondiabetic controls, indicating a chronic procoagulant state. Acutely normalizing hyperglycemia over 2-4 h resulted in a small ( similar to 7%) but significant decline in TF-PCA with no further decline over 24 h. Raising insulin levels alone raised TF-PCA by 30%, whereas raising insulin and glucose levels together increased TF-PCA ( by 80%), thrombin-antithrombin complexes, and prothrombin fragment 1.2. Plasma FVIIa and FVIIc declined with increases in TF-PCA. Conclusion: We conclude that the combination of hyperglycemia and hyperinsulinemia, common in poorly controlled patients with T2DM, contributes to a procoagulant state that may predispose these patients to acute cardiovascular events.
引用
收藏
页码:4352 / 4358
页数:7
相关论文
共 29 条
[1]  
Abdel-Hafiz E, 2002, BLOOD, V100, p496A
[2]   Differential effects of somatostatin on circulating tissue factor procoagulant activity and protein [J].
Boden, Guenther ;
Vaidyula, Vijender ;
Homko, Carol ;
Mozzoli, Maria ;
Rao, A. Koneti .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2007, 292 (05) :E1333-E1339
[3]   Hematopoietic cell-derived microparticle tissue factor contributes to fibrin formation during thrombus propagation [J].
Chou, J ;
Mackman, N ;
Merrill-Skoloff, G ;
Pedersen, B ;
Furie, BC ;
Furie, B .
BLOOD, 2004, 104 (10) :3190-3197
[4]   INSULIN RESISTANCE - A MULTIFACETED SYNDROME RESPONSIBLE FOR NIDDM, OBESITY, HYPERTENSION, DYSLIPIDEMIA, AND ATHEROSCLEROTIC CARDIOVASCULAR-DISEASE [J].
DEFRONZO, RA ;
FERRANNINI, E .
DIABETES CARE, 1991, 14 (03) :173-194
[5]   HYPERINSULINEMIA AS A PREDICTOR OF CORONARY HEART-DISEASE MORTALITY IN A HEALTHY POPULATION - THE PARIS PROSPECTIVE-STUDY, 15-YEAR FOLLOW-UP [J].
FONTBONNE, A ;
CHARLES, MA ;
THIBULT, N ;
RICHARD, JL ;
CLAUDE, JR ;
WARNET, JM ;
ROSSELIN, GE ;
ESCHWEGE, E .
DIABETOLOGIA, 1991, 34 (05) :356-361
[6]   Blood-borne tissue factor:: Another view of thrombosis [J].
Giesen, PLA ;
Rauch, U ;
Bohrmann, B ;
Kling, D ;
Roqué, M ;
Fallon, JT ;
Badimon, JJ ;
Himber, J ;
Riederer, MA ;
Nemerson, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) :2311-2315
[7]   DIABETES, FIBRINOGEN, AND RISK OF CARDIOVASCULAR-DISEASE - THE FRAMINGHAM EXPERIENCE [J].
KANNEL, WB ;
DAGOSTINO, RB ;
WILSON, PWF ;
BELANGER, AJ ;
GAGNON, DR .
AMERICAN HEART JOURNAL, 1990, 120 (03) :672-676
[8]   ACTIVATION OF TISSUE FACTOR-INDUCED COAGULATION AND ENDOTHELIAL-CELL DYSFUNCTION IN NON-INSULIN-DEPENDENT DIABETIC-PATIENTS WITH MICROALBUMINURIA [J].
KARIO, K ;
MATSUO, T ;
KOBAYASHI, H ;
MATSUO, M ;
SAKATA, T ;
MIYATA, T .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1995, 15 (08) :1114-1120
[9]   Whole blood tissue factor procoagulant activity is elevated in patients with sickle cell disease [J].
Key, NS ;
Slungaard, A ;
Dandelet, L ;
Nelson, SC ;
Moertel, C ;
Styles, LA ;
Kuypers, FA ;
Bach, RR .
BLOOD, 1998, 91 (11) :4216-4223
[10]   CHANGES IN BLOOD-COAGULATION, PLATELET-FUNCTION, AND PLASMINOGEN-PLASMIN SYSTEM IN DIABETES [J].
KWAAN, HC .
DIABETES, 1992, 41 :32-35