Cigarette smoking is independently associated with markers of endothelial dysfunction and hyperinsulinaemia in non-diabetic individuals with coronary artery disease

被引:36
作者
Winkelmann, BR
Boehm, BO
Nauck, M
Kleist, P
März, W
Verhoe, NK
Ranjith, N
Kneissl, G
机构
[1] Univ Klinikum Heidelberg, Kooperat Einheit Pharmakogenom Angew Genomforsch, D-69120 Heidelberg, Germany
[2] Univ Ulm Klinikum, Sekt Endokrinol, Ulm, Germany
[3] Univ Freiburg Klinikum, Freiburg, Germany
[4] Novartis Pharma Schweiz AG, Dept Med, Bern, Switzerland
[5] Univ Vienna, A-1010 Vienna, Austria
[6] Kardiol Gemeinschaftspraxis, Leipzig, Germany
关键词
cigarette smoking; endothelial dysfunction; cell adhesion molecule; hyperinsulinaemia; insulin resistance; coronary artery disease;
D O I
10.1185/0300799039117049
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background, Oxidative stress and endothelial dysfunction have been introduced as a unifying pathological mechanism for early atherosclerotic disease. They are caused by a variety of stimuli including cigarette smoking (environmental) and type 2 diabetes (disease factor), However, the role of hyperinsulininaemia, a marker of insulin resistance, as a risk factor for atherosclerosis remains to be clarified. Study objectives: To study the relationship of smoking, hyperinsulinaemia and biochemical markers of oxidative stress and endothelial dysfunction, in patients with coronary artery disease. Design: Case-control study of 5-year survivor status in smokers, former smokers and nonsmokers with angiographically documented stable coronary artery disease classified by self-reporting of smoking status together with plasma cotinine measurements. Setting: Cardiology and cardiac surgery unit of a tertiary care referral centre. Patients and methods: Plasma levels of vitamins C, E and selenium, and the adhesion molecules E-selectin, intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) were assessed In 214 patients at baseline together with the glucose and insulin response to an oral glucose challenge. Sixty known or newly diagnosed type 2 diabetic patients (28%) were identified and excluded from further analysis. Results: E-selectin and ICAM-1, serving as markers of endothelial dysfunction, significantly correlated with hyperinsulinaemia (p < 0.5). Circulating immunoreactive insulin was elevated in active smokers and former smokers as compared to non-smokers after an oral glucose load (p < 0.05 for the area under the insulin time curve), despite a similar glucose response, Smoking was associated with a decrease in antioxidant vitamins C (p = 0.02) and E (p =0.03), and an increase of E-selectin (p < 0.05) and ICAM-1 (p < 0.001), Low baseline ICAM-1 and high vitamin C levels emerged as the most significant multivariate predictors of 5-year survival (p < 0.001). Conclusions: Hyperinsulinaemia in smokers Is linked with markers of endothelial dysfunction. Impaired vascular reactivity can thus be a new possible mechanism linking insulin resistance and smoking.
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收藏
页码:132 / 141
页数:10
相关论文
共 53 条
[1]   Cigarette smoking is associated with increased human monocyte adhesion to endothelial cells: Reversibility with oral L-arginine but not vitamin C [J].
Adams, MR ;
Jessup, W ;
Celermajer, DS .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1997, 29 (03) :491-497
[2]   SMOKING INDUCES INSULIN RESISTANCE - A POTENTIAL LINK WITH THE INSULIN RESISTANCE SYNDROME [J].
ATTVALL, S ;
FOWELIN, J ;
LAGER, I ;
VONSCHENCK, H ;
SMITH, U .
JOURNAL OF INTERNAL MEDICINE, 1993, 233 (04) :327-332
[3]   LIPID INTOLERANCE IN SMOKERS [J].
AXELSEN, M ;
ELIASSON, B ;
JOHEIM, E ;
LENNER, RA ;
TASKINEN, MR ;
SMITH, U .
JOURNAL OF INTERNAL MEDICINE, 1995, 237 (05) :449-455
[4]   Insulin and coronary artery disease: Is syndrome X the unifying hypothesis? [J].
Baillie, GM ;
Sherer, JT ;
Weart, CW .
ANNALS OF PHARMACOTHERAPY, 1998, 32 (02) :233-247
[5]   Persistent elevation of plasma insulin levels is associated with increased cardiovascular risk in children and young adults - The Bogalusa Heart Study [J].
Bao, WH ;
Srinivasan, SR ;
Berenson, GS .
CIRCULATION, 1996, 93 (01) :54-59
[6]   NICOTINE AND COTININE ELIMINATION PHARMACOKINETICS IN SMOKERS AND NONSMOKERS [J].
BENOWITZ, NL ;
JACOB, P .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1993, 53 (03) :316-323
[7]   Insulin resistance and coronary artery disease [J].
Bressler, P ;
Bailey, SR ;
Matsuda, M ;
DeFronzo, RA .
DIABETOLOGIA, 1996, 39 (11) :1345-1350
[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]  
CERASI E, 1973, LANCET, V1, P794
[10]   Impaired glucose transport as a cause of decreased insulin-stimulated muscle glycogen synthesis in type 2 diabetes [J].
Cline, GW ;
Petersen, KF ;
Krssak, M ;
Shen, J ;
Hundal, RS ;
Trajanoski, Z ;
Inzucchi, S ;
Dresner, A ;
Rothman, DL ;
Shulman, GI .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (04) :240-246