基本情報
- 所属
- 自治医科大学 医学部薬理学講座臨床薬理学部門 教授医学部内科学講座循環器内科学部門 教授(兼)
- 学位
- 医学博士(東京大学)
- J-GLOBAL ID
- 201401001007364738
- researchmap会員ID
- B000238134
- 外部リンク
研究キーワード
6研究分野
1経歴
4-
2017年4月 - 現在
-
2017年4月 - 現在
-
2013年11月 - 2017年3月
-
2012年3月 - 2013年10月
学歴
2-
1997年4月 - 2001年3月
-
1988年4月 - 1994年3月
論文
168-
Journal of cardiology 85(2) 115-176 2025年2月
-
Open Heart 11(2) e002987-e002987 2024年12月23日Background Hypertension is a risk factor for bleeding events and is included in the HAS-BLED (Hypertension, Abnormal renal/liver function, Stroke, Bleeding history or predisposition, Labile INR, Elderly, Drugs/Alcohol concomitantly) score. However, the effects of blood pressure (BP) and changes in BP on bleeding events in patients undergoing percutaneous coronary intervention (PCI) remain poorly understood. This study is aimed to investigate the relationship between systolic BP (SBP) changes during hospitalisation and bleeding events in patients undergoing PCI. Methods From the Clinical Deep Data Accumulation System database, a multicentre database encompassing seven tertiary medical hospitals in Japan that includes data for patient characteristics, medications, laboratory tests, physiological tests, cardiac catheterisation and PCI treatment, data for 6351 patients undergoing PCI between April 2013 and March 2019 were obtained. The study population was categorised into three groups based on the changes in SBP during hospitalisation: (1) elevated BP (≥20 mm Hg), (2) no change (≥−20 to <20 mm Hg) and (3) decreased BP (<−20 mm Hg) groups. The primary outcome was a 3-year major bleeding event defined as moderate or severe bleeding according to the Global Use of Streptokinase and t-PA for Occluded Coronary Arteries bleeding criteria. Results The elevated BP group exhibited significantly lower SBP at admission and higher SBP at discharge (p<0.001). Multivariable Cox hazard regression models showed that elevated BP was associated with a high risk of bleeding events (HR: 1.885; 95% CI, 1.294 to 2.748). The multivariable logistic regression model identified female sex, chronic coronary syndrome, peripheral artery disease and chronic kidney disease as independent factors associated with elevated BP. Conclusions These findings suggest that BP management is essential to prevent bleeding events after PCI.
-
IJC Heart & Vasculature 54 101507-101507 2024年10月 責任著者BACKGROUND: Polypharmacy is associated with an increased risk of adverse events due to the higher number of drugs used. This is particularly notable in patients with chronic coronary syndrome (CCS), who are known to use a large number of drugs. Therefore, we investigated polypharmacy in patients with CCS, using CLIDAS, a multicenter database of patients who underwent percutaneous coronary intervention. METHOD AND RESULTS: Between 2017 and 2020, 1411 CCS patients (71.5 ± 10.5 years old; 77.3 % male) were enrolled. The relationship between cardiovascular events occurring during the median follow-up of 514 days and the number of drugs at the time of PCI was investigated. The median number of drugs prescribed was nine. Major adverse cardiovascular events (MACE), defined as cardiovascular death, myocardial infarction, stroke, heart failure, transient ischemic attack, or unstable angina, occurred in 123 patients, and all-cause mortality occurred in 68 patients. For each additional drug, the adjusted hazard ratios for MACE and all-cause mortality increased by 2.069 (p = 0.003) and 1.102 (p = 0.010). The adjusted hazard ratios for MACE and all-cause mortality were significantly higher in the group using nine or more drugs compared to the group using eight or fewer drugs (1.646 and 2.253, both p < 0.001). CONCLUSION: This study showed that an increase in the number of drugs used for CCS may be associated with MACE and all-cause mortality. In patients with CCS, it might be beneficial to minimize the number of medications as much as possible, while managing comorbidities and using guideline-recommended drugs.
-
Circulation journal : official journal of the Japanese Circulation Society 88(12) 2022-2099 2024年9月27日 筆頭著者責任著者
-
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
288-
Circulation journal : official journal of the Japanese Circulation Society 67 634-634 2003年3月1日
-
Circulation journal : official journal of the Japanese Circulation Society 67 423-423 2003年3月1日
-
Circulation journal : official journal of the Japanese Circulation Society 67 216-216 2003年3月1日
-
Circulation journal : official journal of the Japanese Circulation Society 67 195-195 2003年3月1日
-
Circulation journal : official journal of the Japanese Circulation Society 67 153-153 2003年3月1日
-
Circulation journal : official journal of the Japanese Circulation Society 67 153-153 2003年3月1日
-
Circulation journal : official journal of the Japanese Circulation Society 67 146-146 2003年3月1日
-
Circulation journal : official journal of the Japanese Circulation Society 67 307-307 2003年3月1日
-
Nippon rinsho. Japanese journal of clinical medicine 61 775-780 2003年
-
CIRCULATION 106(19) 215-215 2002年11月
-
CIRCULATION 106(19) 188-189 2002年11月
-
CIRCULATION 106(19) 107-107 2002年11月
-
Circulation journal : official journal of the Japanese Circulation Society 66 120-120 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 706-706 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 386-386 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 283-283 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 437-437 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 431-431 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 787-787 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 586-586 2002年3月31日
-
TAF-1 is a transcriptional cofactor that represses activation by the transcription factor IKLF/BTEB2Circulation journal : official journal of the Japanese Circulation Society 66 464-464 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 263-263 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 263-263 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 265-265 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 220-220 2002年3月31日
-
Circulation journal : official journal of the Japanese Circulation Society 66 169-169 2002年3月31日
-
THROMBOSIS AND HAEMOSTASIS 85(2) 226-230 2001年2月The platelet-collagen receptor, glycoprotein Ia/IIa (integrin alpha (2)beta (1)) plays a fundamental role in the adhesion of platelets to fibrillar collagen, an event leading to platelet activation and thrombus formation and contributing to the pathogenesis of thrombotic disease. Further, glyco protein Ia/IIa receptor density and function may be associated with two linked and silent polymorphisms (C-807/T and (873)G/A) within the glycoprotein Ia gene. We tested the extent to which these polymorphisms serve as genetic markers of myocardial infarction in a Japanese population. A case-control study was carried out using 210 Japanese myocardial infarction patients and 420 age- and sex-matched controls. Genotyping was accomplished using PCR followed by melting curve analysis with specific fluorescent hybridization probes. The (CC)-C-807. CT, TT genotypes linked perfectly to the (873)GG, GA, AA genotypes, respectively. Allele frequencies of the T-807 ((873)A) variant were similar in the control and patient groups (0.373 vs. 0.352). The T-807 and (873)A variants of platelet glycoprotein la gene are common and in a perfect linkage in the Japanese population, but it appears unlikely that the T-807 ((873)A) variant represents a useful marker of increased risk for myocardial infarction.
-
The Journal of biological chemistry 275(47) 36991-8 2000年11月24日Ca(2+), which enters cardiac myocytes through voltage-dependent Ca(2+) channels during excitation, is extruded from myocytes primarily by the Na(+)/Ca(2+) exchanger (NCX1) during relaxation. The increase in intracellular Ca(2+) concentration in myocytes by digitalis treatment and after ischemia/reperfusion is also thought to result from the reverse mode of the Na(+)/Ca(2+) exchange mechanism. However, the precise roles of the NCX1 are still unclear because of the lack of its specific inhibitors. We generated Ncx1-deficient mice by gene targeting to determine the in vivo function of the exchanger. Homozygous Ncx1-deficient mice died between embryonic days 9 and 10. Their hearts did not beat, and cardiac myocytes showed apoptosis. No forward mode or reverse mode of the Na(+)/Ca(2+) exchange activity was detected in null mutant hearts. The Na(+)-dependent Ca(2+) exchange activity as well as protein content of NCX1 were decreased by approximately 50% in the heart, kidney, aorta, and smooth muscle cells of the heterozygous mice, and tension development of the aortic ring in Na(+)-free solution was markedly impaired in heterozygous mice. These findings suggest that NCX1 is required for heartbeats and survival of cardiac myocytes in embryos and plays critical roles in Na(+)-dependent Ca(2+) handling in the heart and aorta.
-
CIRCULATION 102(18) 183-183 2000年10月
-
THROMBOSIS AND HAEMOSTASIS 84(1) 137-137 2000年7月
-
CIRCULATION 98(17) 604-605 1998年10月
書籍等出版物
13共同研究・競争的資金等の研究課題
13-
日本学術振興会 科学研究費助成事業 2022年4月 - 2025年3月
-
日本学術振興会 科学研究費助成事業 2022年4月 - 2025年3月
-
日本学術振興会 科学研究費助成事業 2020年4月 - 2025年3月
-
日本学術振興会 科学研究費助成事業 2020年4月 - 2025年3月
-
日本学術振興会 科学研究費助成事業 2020年7月 - 2023年3月