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Featured researches published by Izuru Nakae.


Heart and Vessels | 2000

Age-dependent impairment of coronary collateral development in humans

Izuru Nakae; Masuo Fujita; Kunihisa Miwa; Koji Hasegawa; Yasuki Kihara; Ryuji Nohara; Shoichi Miyamoto; Kinzo Ueda; Shunichi Tamaki; Shigetake Sasayama

Abstract The purpose of this study was to evaluate whether age influences collateral development in patients with coronary artery disease. The extent of collateral development to the area perfused by the infarct-related artery was graded, depending on the degree of opacification of the occluded infarct-related artery. We evaluated the extent of collateral development using coronary cineangiography in 102 patients with an acutely occluded infarct-related coronary artery within 12 h after the onset of the first acute myocardial infarction, and who had a history of long-standing effort angina. Well-developed collateral circulation was observed in 54 (53%) of the patients. The patients were divided into two groups based on their age. The prevalence of well-developed collateral circulation in the younger group (≤64 years, n = 48) was 69% (33 of 48), being significantly (P = 0.003) higher than 39% (21 of 54) in the older group (≥65 years, n = 54). We conclude that in the presence of stimuli for collateral development i.e., long-standing effort angina accompanied by severe coronary stenosis, the age of patients is a key determinant of collateral development.


Journal of the American College of Cardiology | 1996

Relation between preexistent coronary collateral circulation and the incidence of restenosis after successful primary coronary angioplasty for acute myocardial infarction.

Izuru Nakae; Masatoshi Fujita; Tetsuro Fudo; Tomoyuki Iwase; Terumitsu Tanaka; Shunichi Tamaki; Ryuji Nohara; Shigetake Sasayama

OBJECTIVES The purpose of this study was to test the hypothesis that the incidence of restenosis after primary percutaneous transluminal coronary angioplasty for acute myocardial infarction is largely influenced by the preexistent coronary collateral circulation to the infarct-related coronary artery. BACKGROUND The occurrence of restenosis after coronary angioplasty is the most serious limitation of this procedure. However, prediction of restenosis is difficult. Severe preexistent stenosis of the infarct-related coronary artery causing the development of collateral circulation may result in a high frequency of restenosis. METHODS The study group consisted of 152 consecutive patients undergoing primary coronary angioplasty within 12 h after the onset of a first acute myocardial infarction. Of this group, 124 patients were angiographically followed up during the convalescent period of infarction and were classified into two groups according to the extent of preexistent collateral circulation to the infarct-related coronary artery. RESULTS Restenosis occurred in 26 (38%) of 69 patients with poor or no collateral circulation (group A) in contrast to 35 (64%) of 55 patients with good angiographic collateral circulation (group B, p < 0.005). The frequency of preinfarction angina was significantly lower (p < 0.05) in group A (26% [18 of 69]) than in group B (44% [24 of 55]). CONCLUSIONS These findings indicate that the presence of well developed collateral circulation to the infarct-related coronary artery predicts a higher frequency of restenosis after primary coronary angioplasty. The difference in restenosis rates observed between the patients with and without good collateral circulation probably reflects the impact of underlying severity of stenosis on the long-term outcome after coronary angioplasty.


Journal of the American College of Cardiology | 1997

Fate of Collateral Vessels After Successful Coronary Angioplasty in Patients With Effort Angina

Masatoshi Fujita; Izuru Nakae; Tetsuro Fudo; Terumitsu Tanaka; Tomoyuki Iwase; Shunichi Tamaki; Ryuji Nohara; Shigetake Sasayama

OBJECTIVES The purpose of the present study was to evaluate whether severe restenosis after percutaneous transluminal coronary angioplasty (PTCA) promotes collateral development and whether successful dilation regresses collateral vessels. BACKGROUND It is well known that in the presence of severe coronary stenosis, native collateral arterioles mature to small coronary arteries with several layers of smooth muscle cells. However, it remains unclear whether well developed collateral vessels regress after removal of coronary stenosis. METHODS The study group comprised 41 patients who underwent elective PTCA for effort angina due to single-vessel disease, followed by repeat PTCA to treat restenosis. We classified the patients into three groups depending on the change in baseline Thrombolysis in Myocardial Infarction (TIMI) flow grade of the ischemia-related artery at initial and repeat PTCA, and we compared the extent of ST segment elevation at 1 min of the first balloon inflation between the two procedures. The average interval from initial to repeat PTCA was 125 days. RESULTS The three patient groups comprised group A, 12 patients with decreased flow grade because of severe coronary restenosis; group B, 12 patients with increased flow grade who had severe initial stenosis and relatively mild restenosis; and group C, 17 patients with unchanged flow grade. In the presence of comparable rate-pressure products at initial and repeat PTCA, patients in group A had significantly greater ST segment elevation (p < 0.01) at initial than at repeat PTCA (mean +/- SD 0.42 +/- 0.31 vs. 0.13 +/- 0.22 mV). In group B, ST segment elevation was significantly less at initial than at repeat PTCA (0.13 +/- 0.25 vs. 0.19 +/- 0.17 mV, p < 0.05), and in group C, it was comparable at the two procedures (0.37 +/- 0.32 vs. 0.35 +/- 0.33 mV, p = 0.50). CONCLUSIONS These findings indicate that severe restenosis after PTCA promotes collateral development and that successful dilaton regresses collateral vessels during a relatively short period of time.


Lipids | 2010

Pitavastatin Reduces Lectin-Like Oxidized Low-Density Lipoprotein Receptor-1 Ligands in Hypercholesterolemic Humans

Tetsuya Matsumoto; Masatoshi Fujita; Tatsuya Sawamura; Akemi Kakino; Yuko Sato; Yoshiko Fujita; Haruo Matsuda; Mamoru Nakanishi; Kagehiro Uchida; Izuru Nakae; Hiroshi Kanda; Akira Yoshida; Kunihisa Miwa; Hideki Hayashi; Kenichi Mitsunami; Minoru Horie


Japanese Circulation Journal-english Edition | 2001

Effect of angiotensin-converting enzyme inhibition on sympathetic tone in patients with mild to moderate heart failure.

Moriaki Inoko; Masatoshi Fujita; Izuru Nakae; Shunichi Tamaki; Masato Watanuki; Tetsuo Hashimoto; Takashi Konishi


International Journal of Cardiology | 2014

Pitavastatin decreases serum LOX-1 ligand levels and MT1-MMP expression in CD14-positive mononuclear cells in hypercholesterolemic patients

Hiroyasu Uzui; Hideki Hayashi; Izuru Nakae; Tetsuya Matsumoto; Hiroaki Uenishi; Hisae Hayasaki; Takayoshi Asaji; Shinobu Matsui; Kunihisa Miwa; Jong-Dae Lee; Hiroshi Tada; Tatsuya Sawamura; Masatoshi Fujita


Archive | 2010

collateral circulation in patients with effort angina Improvement of exercise capacity by sarpogrelate as a result of augmented

Yasuki Kihara; Ryuji Nohara; Shigetake Sasayama; Terumitsu Tanaka; Masatoshi Fujita; Izuru Nakae; Shunichi Tamaki; Koji Hasegawa


The journal of Japan Atherosclerosis Society | 2002

Effects of alacepril on low-density lipoprotein particle size in patients with essential hypertension

Kunihisa Miwa; Masatoshi Fujita; Teturo Fudo; Syoichi Miyamoto; Izuru Nakae


Archive | 1998

Automatic processing of myocardial contrast echocardiograms of intravenous injection of contrast

Yoko Yamamoto; Masatoshi Fujita; Yasuki Kihara; Hiroyuki Sekiguchi; Shigeru Eiho; Izuru Nakae; Shigeru Kubo


Journal of the American College of Cardiology | 1998

Improvement of exercise capacity by sarpogrelate as a result of increased collateral blood flow in patients with effort angina

Terumitsu Tanaka; Masatoshi Fujita; A. Tsubokawa; Izuru Nakae; Tomoyuki Iwase; Kinzo Ueda; Shunichi Tamaki; Ryuji Nohara; Shigetake Sasayama

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Shunichi Tamaki

Takeda Pharmaceutical Company

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Tatsuo Fujioka

Takeda Pharmaceutical Company

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