Association of Toll-Like Receptor 4 on Human Monocyte Subsets and Vulnerability Characteristics of Coronary Plaque as Assessed by 64-Slice Multidetector Computed Tomography

  • Ozaki Yuichi
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Imanishi Toshio
    Department of Cardiovascular Medicine, Wakayama Medical University Department of Cardiovascular Medicine, Hidaka General Hospital
  • Hosokawa Seiki
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Nishiguchi Tsuyoshi
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Taruya Akira
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Tanimoto Takashi
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Kuroi Akio
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Yamano Takashi
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Matsuo Yoshiki
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Ino Yasushi
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Kitabata Hironori
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Kubo Takashi
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Tanaka Atsushi
    Department of Cardiovascular Medicine, Wakayama Medical University
  • Akasaka Takashi
    Department of Cardiovascular Medicine, Wakayama Medical University

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抄録

<p>Background:Although Toll-like receptor 4 (TLR-4) is involved in monocyte activation in patients with accelerated forms of atherosclerosis, the relationship between the expression of TLR-4 on circulating monocytes and coronary plaque vulnerability has not previously been evaluated. We investigated this relationship using 64-slice multidetector computed tomography (MDCT) in patients with stable angina pectoris (SAP).</p><p>Methods and Results:We enrolled 65 patients with SAP who underwent MDCT. Three monocyte subsets (CD14++CD16, CD14++CD16+, and CD14+CD16+) and expression of TLR-4 were measured by flow cytometry. Intracoronary plaques were assessed by 64-slice MDCT. We defined vulnerability of intracoronary plaques according to the presence of positive remodeling (remodeling index >1.05) and/or low CT attenuation (<35 HU). The circulating CD14++CD16+monocytes more frequently expressed TLR-4 than CD14++CD16and CD14+CD16+monocytes (P<0.001). The relative proportion of the expression of TLR-4 on CD14++CD16+monocytes was significantly greater in patients with vulnerable plaque compared with those without (10.4 [4.1–14.5] % vs. 4.5 [2.8–7.8] %, P=0.012). In addition, the relative proportion of TLR-4 expression on CD14++CD16+monocytes positively correlated with the remodeling index (r=0.28, P=0.025) and negatively correlated with CT attenuation value (r=−0.31, P=0.013).</p><p>Conclusions:Upregulation of TLR-4 on CD14++CD16+monocytes might be associated with coronary plaque vulnerability in patients with SAP.</p>

収録刊行物

  • Circulation Journal

    Circulation Journal 81 (6), 837-845, 2017

    一般社団法人 日本循環器学会

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