Soluble adhesion molecules and C-reactive protein in the progression of silent cerebral infarction in patients with type 2 diabetes mellitus

被引:67
作者
Kawamura, T [1 ]
Umemura, T
Kanai, A
Nagashima, M
Nakamura, N
Uno, T
Nakayama, M
Sano, T
Hamada, Y
Nakamura, J
Hotta, N
机构
[1] Chubu Rosai Hosp, Labour Prevent Med Ctr, Nagoya, Aichi 4558530, Japan
[2] Chubu Rosai Hosp, Dept Metab & Endocrine Internal Med, Nagoya, Aichi 4558530, Japan
[3] Kasugai City Hosp, Dept Neurol, Nagoya, Aichi 4868510, Japan
[4] Nagoya Univ, Grad Sch Med, Dept Internal Med, Div Metab Dis, Nagoya, Aichi 4668550, Japan
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2006年 / 55卷 / 04期
关键词
D O I
10.1016/j.metabol.2005.10.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The purpose of this Study was to investigate the association between the progression of silent cerebral infarction (SCI) and levels of soluble adhesion molecules and high-sensitivity C-reactive protein (hs-CRP) in type 2 diabetic patients. One hundred twenty middle-aged and elderly diabetic patients without histories of vascular events were followed up for a period of 3 years. We measured levels of soluble intercellular adhesion molecule 1 (sICAM-1), vascular cell adhesion molecule 1, E-selectin, and hs-CRP and assessed brain ischemic lesions by magnetic resonance imaging at baseline and 3 years later. Silent cerebral infarction was observed in 13% of the patients at baseline, and these patients were significantly older and had significantly higher blood pressure than those without SCL Thirty-two patients had newly diagnosed SCI after 3 years. There were no significant differences in factors such as age, blood pressure, and diabetic control between patients without SCI and those in whom it was newly diagnosed. However, only sICAM-1 levels, but not the other soluble adhesion molecules or hs-CRP, were associated with the progression of SCI, and this relationship remains after adjustment for risk factors. On the other hand, higher levels of sICAM-1 and hs-CRP at baseline were observed in 7 patients who were excluded from the present study because of the onset of symptomatic cerebral infarction during follow-up. Our present study Suggests that sICAM-1 levels may be a potential marker for SCI, which may lead to future stroke and vascular dementia, and that this marker could be useful in monitoring disease progression and as a surrogate marker in treatment studies. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:461 / 466
页数:6
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