Early carotid atherosclerosis in overweight nondiabetic individuals is associated with subclinical chronic inflammation independent of underlying insulin resistance

被引:24
作者
Balletshofer, BM [1 ]
Haap, M [1 ]
Rittig, K [1 ]
Stock, J [1 ]
Lehn-Stefan, A [1 ]
Häring, HU [1 ]
机构
[1] Univ Tubingen, Dept Endocrinol Metab & Vasc Med, Tubingen, Germany
关键词
glucose clamp technique; tunica intima; body weight; atheriosclerosis; C-reactive protein; insulin resistance; cell adhesion molecules; ultrasonography; cholesterol; glucose tolerance test;
D O I
10.1055/s-2005-861479
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
nOverweight in children and young adults is an increasing problem in Western industrialized countries with potential impact on cardiovascular morbidity. Whether early arterial wall thickening in these subjects mainly results from the often associated insulin resistance syndrome or from increased subclinical chronic inflammation probably triggered by adipose tissue is still under discussion. We therefore determined insulin sensitivity index (ISI) by performing an euglycaemic hyperinsulinaemic glucose clamp (insulin infusion rate 1 mU/kg/min) and high-sensitivity C-reactive protein (hsCRP) levels in relation to the intimamedia thickness (IMT) at the common carotid artery (high resolution ultrasound; 13 MHz) in 81 young (age 33 +/- 1 years), moderately overweight subjects. To reduce the number of confounding variables, subjects with disturbances in glucose metabolism (75 g oral glucose tolerance test) and hypertension were excluded. As expected, higher BMI was positively correlated with increased IMT (r = 0.358; p = 0.001). After multiple regression analysis, hsCRP levels independently correlated to IMT (r=0.251; p = 0.03), even after adjusting for age, sex, BMI, ISI, LDL cholesterol and smoking as cofactors. However, taking all above listed factors into account, glucose-clamp assessed insulin sensitivity was not correlated with IMT. Thus, overweight might trigger inflammatory mechanisms leading to vascular wall hypertrophy independent of the insulin resistance syndrome already early in life.
引用
收藏
页码:331 / 335
页数:5
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