Coronary vasomotor abnormalities in insulin-resistant individuals

被引:131
作者
Quiñones, MJ
Hernandez-Pampaloni, M
Schelbert, H
Bulnes-Enriquez, I
Jimenez, X
Hernandez, G
De la Rosa, R
Chon, Y
Yang, HY
Nicholas, SB
Modilevsky, T
Yu, K
Van Herle, K
Castellani, LW
Elashoff, R
Hsueh, WA
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Div Endocrinol Diabet & Hypertens, Cedars Sinai Med Ctr, Los Angeles, CA 90095 USA
[2] Olive View Univ Calif, Los Angeles Med Ctr, Sylmar, CA USA
关键词
D O I
10.7326/0003-4819-140-9-200405040-00009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Insulin resistance is a metabolic spectrum that progresses from hyperinsulinemia to the metabolic syndrome, impaired glucose tolerance, and finally type 2 diabetes mellitus. It is unclear when vascular abnormalities begin in this spectrum of metabolic effects. Objective: To evaluate the association of insulin resistance with the presence and reversibility of coronary vasomotor abnormalities in young adults at low cardiovascular risk. Design: Cross-sectional study followed by prospective, open-label treatment study. Setting: University hospital. Patients: 50 insulin-resistant and 22 insulin-sensitive, age-matched Mexican-American participants without glucose intolerance or traditional risk factors for or evidence of coronary artery disease. Intervention: 3 months of thiazolidinedione therapy for 25 insulin-resistant patients. Measurements: Glucose infusion rate in response to insulin infusion was used to define insulin resistance (glucose infusion rate less than or equal to 4.00 mg/kg of body weight per minute [range, 0.90 to 3.96 mg/kg per minute]) and insulin sensitivity (glucose infusion rate greater than or equal to 7.50 mg/kg per minute [range, 7.52 to 13.92 mg/kg per minute]). Myocardial blood flow was measured by using positron emission tomography at rest, during cold pressor test (largely endothelium-dependent), and after dipyridamole administration (largely vascular smooth muscle-dependent). Results: Myocardial blood flow responses to dipyridamole were similar in the insulin-sensitive and insulin-resistant groups. However, myocardial blood flow response to cold pressor test increased by 47.6% from resting values in insulin-sensitive patients and by 14.4% in insulin-resistant patients. During thiazolidinedione therapy in a subgroup of insulin-resistant patients, insulin sensitivity improved, fasting plasma insulin levels decreased, and myocardial blood flow responses to cold pressor test normalized. Limitations: The study was not randomized, and it included only 1 ethnic group. Conclusions: insulin-resistant patients who do not have hypercholesterolemia or hypertension and do not smoke manifest coronary vasomotor abnormalities. Insulin-sensitizing thiazolidinedione therapy normalized these abnormalities. These results suggest an association between insulin resistance and abnormal coronary vasomotor function, a relationship that requires confirmation in larger studies.
引用
收藏
页码:700 / 708
页数:9
相关论文
共 53 条
[1]  
Amberger A, 1997, CELL STRESS CHAPERON, V2, P94, DOI 10.1379/1466-1268(1997)002<0094:CEOIVE>2.3.CO
[2]  
2
[3]   Insulin causes endothelial dysfunction in humans - Sites and mechanisms [J].
Arcaro, G ;
Cretti, A ;
Balzano, S ;
Lechi, A ;
Muggeo, M ;
Bonora, E ;
Bonadonna, RC .
CIRCULATION, 2002, 105 (05) :576-582
[4]   Endothelial dysfunction is detectable in young normotensive first-degree relatives of subjects with type 2 diabetes in association with insulin resistance [J].
Balletshofer, BM ;
Rittig, K ;
Enderle, MD ;
Volk, A ;
Maerker, E ;
Jacob, S ;
Matthaei, S ;
Rett, K ;
Häring, HU .
CIRCULATION, 2000, 101 (15) :1780-1784
[5]   ACRP30/adiponectin: an adipokine regulating glucose and lipid metabolism [J].
Berg, AH ;
Combs, TP ;
Scherer, PE .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2002, 13 (02) :84-89
[6]   Inflammatory cytokines impair endothelium-dependent dilatation in human veins in vivo [J].
Bhagat, K ;
Vallance, P .
CIRCULATION, 1997, 96 (09) :3042-3047
[7]   Glucose tolerance and cardiovascular mortality -: Comparison of fasting and 2-hour diagnostic criteria [J].
Borch-Johnsen, K ;
Neil, A ;
Balkau, B ;
Larsen, S ;
Nissinen, A ;
Pekkanen, J ;
Tuomilehto, J ;
Jousilahti, P ;
Lindstrom, J ;
Pyörälä, M ;
Pyörälä, K ;
Eschwege, E ;
Gallus, G ;
Garancini, MP ;
Bouter, LM ;
Dekker, JM ;
Heine, RJ ;
Nijpels, HG ;
Stehouwer, CDA ;
Feskens, EJM ;
Kromhout, D ;
Peltonen, M ;
Pajak, A ;
Eriksson, J ;
Qiao, Q .
ARCHIVES OF INTERNAL MEDICINE, 2001, 161 (03) :397-405
[8]   Microvascular and macrovascular reactivity is reduced in subjects at risk for type 2 diabetes [J].
Caballero, AE ;
Arora, S ;
Saouaf, R ;
Lim, SC ;
Smakowski, P ;
Park, JY ;
King, GL ;
LoGerfo, FW ;
Horton, ES ;
Veves, A .
DIABETES, 1999, 48 (09) :1856-1862
[9]   Diabetes and endothelial dysfunction: A clinical perspective [J].
Calles-Escandon, J ;
Cipolla, M .
ENDOCRINE REVIEWS, 2001, 22 (01) :36-52
[10]   Effects of long-term smoking on myocardial blood flow, coronary vasomotion, and vasodilator capacity [J].
Campisi, R ;
Czernin, J ;
Schöder, H ;
Sayre, JW ;
Marengo, FD ;
Phelps, ME ;
Schelbert, HR .
CIRCULATION, 1998, 98 (02) :119-125