Beneficial effect of anti-platelet therapies on atherosclerotic lesion formation assessed by phase-contrast X-ray CT imaging
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  • 作者:Masafumi Takeda (1)
    Tomoya Yamashita (1) tomoya@med.kobe-u.ac.jp
    Masakazu Shinohara (1)
    Naoto Sasaki (1)
    Hideto Tawa (1)
    Kenji Nakajima (1)
    Atsushi Momose (2)
    Ken-ichi Hirata (1)
  • 关键词:Anti ; platelet therapy – ; Phase ; contrast X ; ray CT imaging – ; Plaque stability – ; Inflammation
  • 刊名:The International Journal of Cardiovascular Imaging (formerly Cardiac Imaging)
  • 出版年:2012
  • 出版时间:June 2012
  • 年:2012
  • 卷:28
  • 期:5
  • 页码:1181-1191
  • 全文大小:546.6 KB
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  • 作者单位:1. Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, 7-5-2 Kusunoki-cho, Chuo-ku, Kobe, 650-0017 Japan2. Department of Advanced Materials Science, Graduate School of Frontier Sciences, The University of Tokyo, Tokyo, Japan
  • ISSN:1573-0743
文摘
We have applied an imaging system of phase-contrast X-ray CT to the detection of atherosclerotic plaque components by means of the differences of tissue mass densities. In this study, we investigated the effect of the anti-platelet therapies, widely used for secondly prevention of cardiovascular events, on plaque stability and examined whether this novel technique could detect the changes of plaque components under the therapy. Apolipoprotein E-deficient mice were fed on high-cholesterol diet alone and either with 0.1% cilostazol or clopidogrel for 10 weeks. We assessed atherosclerotic lesion volumes and components at brachiocephalic artery by the phase-contrast X-ray CT imaging and histochemistry. The phase-contrast X-ray CT imaging could reveal that cilostazol and clopidogrel significantly decreased atherosclerotic lesion volumes at brachiocephalic artery (31.2% reduction in cilostazol group and 37.4% reduction in clopidogrel group), compared with control group. In addition, the mass densities calculated by this method revealed the anti-platelet treatment increased stable plaque areas including high collagen content, but decreased unstable plaque areas including lipid and macrophage content. These findings were confirmed by histological analyses. Real-time PCR analyses indicated that anti-platelets inhibited gene expressions of cytokines and adhesion molecules, such as IFNγ and ICAM-1. Anti-platelet therapies had a beneficial effect on plaque stability maybe due to anti-inflammatory actions. Phase-contrast X-ray CT imaging could quantify the plaque volume and qualify the plaque components affected by anti-platelet therapies. This novel phase-contrast X-ray CT imaging system could be a plausible method to detect the unstable plaque non-invasively in the future.

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