基本情報
研究キーワード
4研究分野
1委員歴
5-
2012年 - 2014年
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2014年
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2014年
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2014年
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2012年
受賞
7-
2010年3月
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2009年5月
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2006年11月
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2002年7月
論文
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Journal of the American Heart Association 14(2) e034627 2025年1月21日BACKGROUND: The effect of worsening renal function and baseline chronic kidney disease (CKD) on outcomes in patients with chronic coronary syndrome in the setting of optimal medical therapy remains unknown. METHODS AND RESULTS: The REAL-CAD (Randomized Evaluation of Aggressive or Moderate Lipid Lowering Therapy With Pitavastatin in Coronary Artery Disease) study is a prospective, multicenter, randomized trial of high-dose (pitavastatin 4 mg/day) or low-dose (pitavastatin 1 mg/day) statin therapy in 12 118 patients with chronic coronary syndrome. The primary end point was a composite of cardiovascular death, nonfatal myocardial infarction, stroke, or unstable angina requiring hospitalization (major adverse cardiac and cerebral events [MACCE]). CKD was defined as an estimated glomerular filtration rate [eGFR] <60 mL/min per 1.73 m2. WRF was defined as a decrease in eGFR ≥20% in the initial year; borderline renal function was an annual decrease of 0%<eGFR<20%, and stable renal function was no decrease. Of 12 118 patients, 4340 had baseline CKD and 7778 did not. The rate of MACCE at 5 years was significantly lower in those without (5.5%) versus with CKD (9.5%) (P<0.0001). After excluding 1247 patients who had MACCE, were censored, or missing eGFR within 1 year, 10 871 patients were included. Of these, 3885 were baseline CKD and the remaining 6986 did not have baseline CKD. Of the 10 871 patients, 577 patients had WRF, 6014 patients showed borderline renal function, and the remaining 4280 patients maintained stable renal function. In patients with CKD, WRF was an independent predictor for MACCE at 4 years as compared with stable renal function (hazard ratio [HR]: 1.67; [95% CI, 1.03-2.73; P=0.039]). In patients without CKD, borderline renal function was a significant predictor for MACCE at 4 years compared with stable renal function (HR: 1.40 [95% CI, 1.03-1.91; P=0.032]). CONCLUSIONS: Baseline CKD was an independent predictor for MACCE in patients with CCS. WRF was a significant predictor for MACCE in patients with CKD. Because borderline renal function was an independent predictor for MACCE even in patients without CKD, mild-to-moderate annual declines of eGFR should be carefully monitored (NCT01042730). REGISTRATION: URL: https://www.clinicaltrials.gov; Unique Identifier: NCT01042730.
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International Journal of Molecular Sciences 26(2) 556-556 2025年1月10日 査読有り
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IJC Heart & Vasculature 54 101507-101507 2024年10月
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Hypertension research : official journal of the Japanese Society of Hypertension 2024年9月19日The Japanese Society of Hypertension have established a blood pressure (BP) target of 130/80 mmHg for patients with coronary artery disease (CAD). We evaluated the data of 8793 CAD patients in the Clinical Deep Data Accumulation System database who underwent cardiac catheterization at six university hospitals and the National Cerebral and Cardiovascular Center (average age 70 ± 11 years, 78% male, 43% with acute coronary syndrome [ACS]). Patients were divided into two groups based on whether or not they achieved the guideline-recommended BP of <130/80 mmHg. We analyzed the relationship between BP classification and major adverse cardiac and cerebral event (MACCE) separately in two groups: those with ACS and those with chronic coronary syndrome (CCS). During an average follow-up period of 33 months, 710 MACCEs occurred. A BP below 130/80 mmHg was associated with fewer MACCEs in both the overall (hazard ratio [HR] 0.83, 95% confidence interval [CI] 0.70-1.00, p = 0.048) and the ACS group (HR 0.67, 95%CI 0.51-0.88, p = 0.003). In particular, stroke events were also lower among those with a BP below 130/80 mmHg in both the overall (HR 0.69, 95%CI 0.53-0.90, p = 0.006) and ACS groups (HR 0.44, 95%CI 0.30-0.67, p < 0.001). In conclusion, the achievement of BP guidelines was associated with improved outcomes in CAD patients, particularly in reducing stroke risk among those with ACS.
MISC
1923-
日本内分泌学会雑誌 80(2) 494-494 2004年9月
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EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING 31 S223-S223 2004年8月
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EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING 31(8) 1218-1218 2004年8月
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American journal of respiratory cell and molecular biology 31(2) 209-15 2004年8月 査読有りEndothelial PAS domain protein-1 (EPAS1) regulates transcription of the genes encoding erythropoietin and vascular endothelial growth factor, which are important for maintaining oxygen homeostasis. We have previously shown that plasminogen activator inhibitor-1 (PAI-1) gene expression is induced by hypoxia. In this study, we sought to determine whether PAI-1 gene expression is directly regulated by EPAS1 in cancer cells because activities of proteases and their inhibitors are tightly regulated for tumor invasion. Hypoxia increased the PAI-1 mRNA levels in human adenocarcinoma A549 cells. Overexpression of EPAS1 significantly increased the PAI-1 mRNA and protein levels. Transient transfection assays revealed that EPAS1 increased PAI-1 gene transcription through a sequence containing 5'-CACGTACA-3' located at -194 (we refer to it as site HREPAI-1) and GT-box located at -78. Electrophoretic gel mobility shift assays revealed that HREPAI-1 serves as a binding site for EPAS1, and Sp1 constitutively binds to GT-box. In conclusion, PAI-1 expression is induced by EPAS1 through HREPAI-1 and through an Sp1-binding site. These results indicate that the PAI-1 gene is a direct target of EPAS1 and suggest the role of EPAS1 and Sp1 in the hypoxic response of cancer cells.
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Journal of Cardiology 44(Suppl.I) 110-110 2004年8月
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Circulation journal : official journal of the Japanese Circulation Society 68 764-764 2004年4月20日
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Circulation journal : official journal of the Japanese Circulation Society 68 782-782 2004年4月20日
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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 45 U733-U733 2004年4月
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EUROPEAN HEART JOURNAL 25(8) 671-679 2004年4月Aims Impaired myocardial vasodilatation during hyperaemic stress with dipyridamole has been documented in hypercholesterolaemics without evidence of ischaemia. This study investigated whether two commonly used hydroxymethylglutaryl coenzyme A reductase inhibitors, simvastatin and pravastatin, are equally effective in restoring myocardial vasodilatation. Methods and results Forty-four hypercholesterolaemics with a low probability of coronary artery disease and 22 controls were studied. Before and after lipid-lowering therapy with simvastatin (n = 22) or pravastatin (n = 22), myocardial blood flow at rest and during dipyridamole loading was measured using positron emission tomography with [N-13]ammonia, and myocardial vasodilatation was assessed. Treatments with simvastatin and pravastatin similarly reduced plasma total cholesterol and plasma low-density lipoprotein cholesterol. Resting myocardial blood flow was comparable in the controls, simvastatin group, and pravastatin group and unchanged after therapy. Myocardial blood flow during dipyridamole loading and myocardial vasodilatation was tower in the two therapy groups before treatment than in the controls. These parameters improved significantly after therapy with simvastatin, whereas no improvement was observed after pravastatin therapy. The per cent change in myocardial vasodilatation after simvastatin therapy was significantly and inversely correlated with per cent changes in plasma lipid fractions. Conclusion Diminished myocardial vasodilatation in hypercholesterolaemics is improved by simvastatin but not by pravastatin, suggesting differences in vascular effects among statins. (C) 2004 The European Society of Cardiology. Published by Elsevier Ltd. All rights reserved.
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Circulation journal : official journal of the Japanese Circulation Society 68 103-103 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 94-94 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 246-247 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 237-237 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 122-122 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 114-114 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 302-302 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 522-522 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 522-523 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 459-459 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 474-475 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 457-458 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 207-207 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 213-214 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 218-218 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 211-211 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 211-211 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 180-180 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 166-166 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 165-165 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 169-169 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 308-308 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 272-272 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 446-446 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 189-189 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 589-589 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 597-597 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 143-144 2004年3月1日
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Circulation journal : official journal of the Japanese Circulation Society 68 18-18 2004年3月1日
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JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY 43(5) 211A-211A 2004年3月
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JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY 43(5) 306A-306A 2004年3月
書籍等出版物
21-
Springer 2009年 (ISBN: 9784431877745)
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Signal Transduction and Cardiac Hypertrophy (Naranjan S. Dhalla, Larry Hryshko, Elissavet Kardami, Pawan K. Singal, KLUWER ACADEMIC PUBLISHERS) 2003年
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Signal Transduction and Cardiac Hypertrophy (Naranjan S. Dhalla, Larry Hryshko, Elissavet Kardami, Pawan K. Singal, KLUWER ACADEMIC PUBLISHERS) 2003年
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Rapid Cycle Real-Time PCR : methods and applications 2001年
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in"The Hypertrophied Heart" 2000年
共同研究・競争的資金等の研究課題
91-
日本学術振興会 科学研究費助成事業 2023年4月 - 2026年3月
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日本学術振興会 科学研究費助成事業 2020年7月 - 2023年3月
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日本学術振興会 科学研究費助成事業 2019年4月 - 2023年3月
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日本学術振興会 科学研究費助成事業 2019年4月 - 2023年3月
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日本学術振興会 科学研究費助成事業 2018年6月 - 2023年3月