Higher levels of interleukin-6 are associated with lower echogenicity of carotid artery plaques

被引:92
作者
Yamagami, H
Kitagawa, K
Nagai, Y
Hougaku, H
Sakaguchi, M
Kuwabara, K
Kondo, K
Masuyama, T
Matsumoto, M
Hori, M
机构
[1] Osaka Univ, Grad Sch Med, Dept Internal Med & Therapeut A8, Suita, Osaka 5650871, Japan
[2] Kobe City Gen Hosp, Dept Neurol, Kobe, Hyogo, Japan
[3] Nishizawa Med Off, Osaka, Japan
[4] Hiroshima Univ, Grad Sch Biomed Sci, Dept Clin Neurosci & Therapeut, Hiroshima, Japan
关键词
atherosclerosis; carotid arteries; inflammation; interleukins; ultrasonography;
D O I
10.1161/01.STR.0000116876.96334.82
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose - Echo-lucent carotid plaques can be fragile and vulnerable to rupture, representing a risk factor for ischemic stroke. Given the studies showing that elevated levels of circulating inflammatory markers are predictive of cardiovascular events, we sought to determine whether higher levels of serum interleukin-6 (IL-6) and high-sensitivity C-reactive protein (hsCRP) are associated with lower echogenicity of carotid plaques. Methods - The study comprised 246 patients who had carotid atherosclerotic plaques as evidenced by ultrasound. Using acoustic densitometry, we quantified the echogenicity of the largest plaque in each patient by integrated backscatter analysis. Serum IL-6 and hsCRP levels were determined in all patients. Results - Both log-transformed IL-6 and hsCRP concentrations were negatively correlated with carotid plaque echogenicity (r = - 0.28, P < 0.001, and r = - 0.14, P < 0.05, respectively). When traditional atherosclerotic risk factors, plaque thickness, and medication use were controlled for, IL-6 levels were inversely associated with plaque echogenicity (beta = - 0.21, P < 0.01), whereas such an association was of borderline significance for hsCRP (beta = - 0.12, P = 0.06). Conclusions - Higher IL-6 levels, in addition to hsCRP levels, appear to be associated with lower echogenicity of carotid plaques, suggesting a link between inflammation and potential risk of plaques.
引用
收藏
页码:677 / 681
页数:5
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