Tomonori Hara
Fujita Health University
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Featured researches published by Tomonori Hara.
Journal of the American College of Cardiology | 2009
Sadako Motoyama; Masayoshi Sarai; Hiroto Harigaya; Hirofumi Anno; Kaori Inoue; Tomonori Hara; Hiroyuki Naruse; Junichi Ishii; Hitoshi Hishida; Nathan D. Wong; Renu Virmani; Takeshi Kondo; Yukio Ozaki; Jagat Narula
OBJECTIVES In a computed tomographic (CT) angiography study, we identified the characteristics of atherosclerotic lesions that were associated with subsequent development of acute coronary syndrome (ACS). BACKGROUND The CT characteristics of culprit lesions in ACS include positive vessel remodeling (PR) and low-attenuation plaques (LAP). These 2 features have been observed in the lesions that have already resulted in ACS, but their prospective relation to ACS has not been previously described. METHODS In 1,059 patients who underwent CT angiography, atherosclerotic lesions were analyzed for the presence of 2 features: PR and LAP. The remodeling index, and plaque and LAP areas and volumes were calculated. The plaque characteristics of lesions resulting in ACS during the follow-up of 27 +/- 10 months were evaluated. RESULTS Of the 45 patients showing plaques with both PR and LAP (2-feature positive plaques), ACS developed in 10 (22.2%), compared with 1 (3.7%) of the 27 patients with plaques displaying either feature (1-feature positive plaques). In only 4 (0.5%) of the 820 patients with neither PR nor LAP (2-feature negative plaques) did ACS develop. None of the 167 patients with normal angiograms had acute coronary events (p < 0.001). ACS was independently predicted by PR and/or LAP (hazard ratio: 22.8, 95% confidence interval: 6.9 to 75.2, p < 0.001). Among 2- or 1-feature positive segments, those resulting in ACS demonstrated significantly larger remodeling index (126.7 +/- 3.9% vs. 113.4 +/- 1.6%, p = 0.003), plaque volume (134.9 +/- 14.1 mm(3) vs. 57.8 +/- 5.7 mm(3), p < 0.001), LAP volume (20.4 +/- 3.4 mm(3) vs. 1.1 +/- 1.4 mm(3), p < 0.001), and percent LAP/total plaque area (21.4 +/- 3.7 mm(2) vs. 7.7 +/- 1.5 mm(2), p = 0.001) compared with segments not resulting in ACS. CONCLUSIONS The patients demonstrating positively remodeled coronary segments with low-attenuation plaques on CT angiography were at a higher risk of ACS developing over time when compared with patients having lesions without these characteristics.
Jacc-cardiovascular Imaging | 2010
Kaori Inoue; Sadako Motoyama; Masayoshi Sarai; Takahisa Sato; Hiroto Harigaya; Tomonori Hara; Yoshihiro Sanda; Hirofumi Anno; Takeshi Kondo; Nathan D. Wong; Jagat Narula; Yukio Ozaki
OBJECTIVES This study sought to assess, by serial computed tomography angiography (CTA), the effect of statin treatment on coronary plaque morphology. BACKGROUND In addition to the assessment of luminal stenosis, CTA also allows characterization of plaque morphology. Large, positively remodeled plaques with large necrotic cores have been reported as indicators of plaque instability. METHODS CTA was performed in 32 patients (26 men, ages 64.3 +/- 8.5 years). Of these, 24 received fluvastatin after the baseline study; 8 subjects who refused statin treatment were followed as the control subjects. Serial imaging was performed after a median interval of 12 months. All vessels were examined in every subject, and a 10-mm-long segment was identified for comparison before and after intervention. Total plaque volume, low attenuation plaque (LAP) volume, lumen volume, and remodeling index were calculated. RESULTS In the statin-treated patients, the total plaque volume (92.3 +/- 37.7 vs. 76.4 +/- 26.5 mm(3), p < 0.01) and LAP volume (4.9 +/- 7.8 vs. 1.3 +/- 2.3 mm(3), p = 0.01) were significantly reduced over time; however, there was no change in the lumen volume (63.9 +/- 25.3 vs. 65.2 +/- 26.2 mm(3), p = 0.59). On the other hand, no change was observed in the CTA characteristics in the control subjects, including total plaque volume (94.4 +/- 21.2 vs. 98.4 +/- 28.6 mm(3), p = 0.48), LAP volume (2.1 +/- 3.0 vs. 2.3 +/- 3.6 mm(3), p = 0.91), and lumen volume (80.5 +/- 20.7 vs. 75.0 +/- 16.3 mm(3), p = 0.26). The plaque volume change (-15.9 +/- 22.2 vs. 4.0 +/- 14.0 mm(3), p = 0.01) and LAP volume change (-3.7 +/- 7.0 vs. 0.2 +/- 1.5 mm(3), p < 0.01) were significantly greater in the statin than the control group. The lumen volume (1.3 +/- 15.6 vs. -5.5 +/- 13.1 mm(3), p = 0.24) and remodeling index (-2.4 +/- 6.8% vs. -0.3 +/- 6.5%, p = 0.53) did not show the significant differences between the 2 groups. The decrease in the plaque volume was due to reduction in the LAP volume (R = 0.83, p < 0.01), and was not related to any changes in the lumen volume (R = 0.21, p = 0.24). CONCLUSIONS This preliminary study suggests that serial CTA evaluation of coronary plaques allows for the assessment of interval change in the plaque morphology. Statin treatment results in decreases in the plaque and necrotic core volume. The features known to be associated with plaque instability.
Jacc-cardiovascular Imaging | 2010
Kaori Inoue; Sadako Motoyama; Masayoshi Sarai; Takahisa Sato; Hiroto Harigaya; Tomonori Hara; Yoshihiro Sanda; Hirofumi Anno; Takeshi Kondo; Nathan D. Wong; Jagat Narula; Yukio Ozaki
OBJECTIVES This study sought to assess, by serial computed tomography angiography (CTA), the effect of statin treatment on coronary plaque morphology. BACKGROUND In addition to the assessment of luminal stenosis, CTA also allows characterization of plaque morphology. Large, positively remodeled plaques with large necrotic cores have been reported as indicators of plaque instability. METHODS CTA was performed in 32 patients (26 men, ages 64.3 +/- 8.5 years). Of these, 24 received fluvastatin after the baseline study; 8 subjects who refused statin treatment were followed as the control subjects. Serial imaging was performed after a median interval of 12 months. All vessels were examined in every subject, and a 10-mm-long segment was identified for comparison before and after intervention. Total plaque volume, low attenuation plaque (LAP) volume, lumen volume, and remodeling index were calculated. RESULTS In the statin-treated patients, the total plaque volume (92.3 +/- 37.7 vs. 76.4 +/- 26.5 mm(3), p < 0.01) and LAP volume (4.9 +/- 7.8 vs. 1.3 +/- 2.3 mm(3), p = 0.01) were significantly reduced over time; however, there was no change in the lumen volume (63.9 +/- 25.3 vs. 65.2 +/- 26.2 mm(3), p = 0.59). On the other hand, no change was observed in the CTA characteristics in the control subjects, including total plaque volume (94.4 +/- 21.2 vs. 98.4 +/- 28.6 mm(3), p = 0.48), LAP volume (2.1 +/- 3.0 vs. 2.3 +/- 3.6 mm(3), p = 0.91), and lumen volume (80.5 +/- 20.7 vs. 75.0 +/- 16.3 mm(3), p = 0.26). The plaque volume change (-15.9 +/- 22.2 vs. 4.0 +/- 14.0 mm(3), p = 0.01) and LAP volume change (-3.7 +/- 7.0 vs. 0.2 +/- 1.5 mm(3), p < 0.01) were significantly greater in the statin than the control group. The lumen volume (1.3 +/- 15.6 vs. -5.5 +/- 13.1 mm(3), p = 0.24) and remodeling index (-2.4 +/- 6.8% vs. -0.3 +/- 6.5%, p = 0.53) did not show the significant differences between the 2 groups. The decrease in the plaque volume was due to reduction in the LAP volume (R = 0.83, p < 0.01), and was not related to any changes in the lumen volume (R = 0.21, p = 0.24). CONCLUSIONS This preliminary study suggests that serial CTA evaluation of coronary plaques allows for the assessment of interval change in the plaque morphology. Statin treatment results in decreases in the plaque and necrotic core volume. The features known to be associated with plaque instability.
Heart and Vessels | 2011
Hiroto Harigaya; Sadako Motoyama; Masayoshi Sarai; Kaori Inoue; Tomonori Hara; Masanori Okumura; Hiroyuki Naruse; Junnichi Ishii; Hitoshi Hishida; Yukio Ozaki
International Journal of Cardiology | 2010
Shankar Kumar Biswas; Masayoshi Sarai; Akira Yamada; Sadako Motoyama; Hiroto Harigaya; Tomonori Hara; Kunihiko Sugimoto; Hiroshi Toyama; Hitoshi Hishida; Yukio Ozaki
International Journal of Cardiovascular Imaging | 2010
Shankar Kumar Biswas; Masayoshi Sarai; Akira Yamada; Hiroshi Toyama; Sadako Motoyama; Hiroto Harigaya; Tomonori Hara; Hiroyuki Naruse; Hitoshi Hishida; Yukio Ozaki
International Journal of Cardiovascular Imaging | 2009
Shankar Kumar Biswas; Masayoshi Sarai; Hiroshi Toyama; Akira Yamada; Sadako Motoyama; Hiroto Harigaya; Tomonori Hara; Masatsugu Iwase; Hitoshi Hishida; Yukio Ozaki
Archive | 2012
Renu Virmani; Takeshi Kondo; Yukio Ozaki; Jagat Narula; Tomonori Hara; Hiroyuki Naruse; Junichi Ishii; Hitoshi Hishida; Nathan D. Wong; Sadako Motoyama; Masayoshi Sarai; Hiroto Harigaya; Hirofumi Anno; Kaori Inoue
Archive | 2009
Shankar Kumar Biswas; Masayoshi Sarai; Hiroshi Toyama; Akira Yamada; Sadako Motoyama; Hiroto Harigaya; Tomonori Hara; Masatsugu Iwase; Hitoshi Hishida; Yukio Ozaki
Japanese Circulation Journal-english Edition | 2009
Shankar Kumar Biswas; Masayoshi Sarai; Tomonori Hara; Hiroto Harigaya; Sadako Motoyama; Akira Yamada; Masanori Okumura; Hiroyuki Naruse; Kaori Inoue; Hitoshi Hishida; Yukio Ozaki