Dobun Hayashi
University of Tokyo
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BMC Cardiovascular Disorders | 2006
Ryuzo Kawamori; Hiroyuki Daida; Yasushi Tanaka; Katsumi Miyauchi; Akira Kitagawa; Dobun Hayashi; Junji Kishimoto; Shunya Ikeda; Yutaka Imai; Tsutomu Yamazaki
BackgroundThe coexistence of type 2 diabetes mellitus and hypertension increases the risk of cardiovascular diseases. The U.K. Prospective Diabetes Study has shown that blood pressure control as well as blood glucose control is efficient for prevention of complications in hypertensive patients with diabetes mellitus. However, some reports have shown that it is difficult to control the blood pressure and the concomitant use of a plurality of drugs is needed in hypertensive patients with diabetes mellitus. In recent years renin-angiotensin system depressants are increasingly used for the blood pressure control in diabetic patients. Particularly in Japan, angiotensin II (A II) antagonists are increasingly used. However, there is no definite evidence of the point of which is efficient for the control, the increase in dose of A II antagonist or the concomitant use of another drug, in hypertensive patients whose blood pressure levels are inadequately controlled with A II antagonist.Methods/DesignHypertensive patients of age 20 years or over with type 2 diabetes mellitus who have been treated by the single use of AII antagonist at usual doses for at least 8 weeks or patients who have been treated by the concomitant use of AII antagonist and an antihypertensive drug other than calcium channel blockers and ACE inhibitors at usual doses for at least 8 weeks are included.DiscussionWe designed a multi-center, prospective, randomized, open label, blinded-endpoint trial, ADVANCED-J, to compare the increases in dose of A II antagonist and the concomitant use of a Ca-channel blocker (amlodipine) and A II antagonist in hypertensive patients with diabetes mellitus, whose blood pressure levels were inadequately controlled with A II antagonist. This study is different from the usual previous studies in that home blood pressures are assessed as indicators of evaluation of blood pressure. The ADVANCED-J study may have much influence on selection of antihypertensive drugs for treatment in hypertensive patients with diabetes mellitus. It is expected to give an important hint for considering the validity of selection of antihypertensive drugs from the aspects not only of the antihypertensive effect but medical cost-effectiveness.
Journal of Anesthesia | 2007
Tomoki Nishiyama; Dobun Hayashi
PurposeDuring the storage of red blood cell concentrates (CRCs), red blood cells are progressively destroyed and free hemoglobin and potassium concentrations increase. In this study, we focused on an electrostatic field that maintains food freshness without freezing, even at less than the freezing point. We hypothesized that the storage of CRCs under an electrostatic field could keep red blood cells in better condition than conventional storage.MethodsEach of 15 packs of 2-day-old CRCs, preserved in MAP (mannitol, adenine, glucose, phosphate, and citrate) solution (MAP-CRC) was divided into 4 smaller equal-size packs and stored at 4°C in a newly developed refrigerator that can generate an electrostatic field. Each group was exposed to a 0-, 500-, 1500-, or 3000-volt (V) electric field for 30 days. Concentrations of free hemoglobin, total haptoglobin, sodium (Na), and potassium (K), and the pH, were measured in the supernatant.ResultsHaptoglobin was not detected. The Na concentration decreased with time but was significantly lower in the 0-V than in the 500-, 1500-, and 3000-V groups. K and free hemoglobin concentrations increased with time, with significantly higher values in the 0-V than in the 500-, 1500-, and 3000-V groups. The pH decreased in the 500-, 1500-, and 3000-V groups, while it did not change in the 0-V group. The pH decrease was smaller in the 500-V than in the 1500- and 3000-V groups.ConclusionStoring MAP-CRC in an electrostatic field of 500 to 3000 V could decrease hemolysis in the preparation. Considering the lower pH decrease, 500 V might be the field of choice.
Journal of Biological Chemistry | 2000
Weidong Zhu; Yunzeng Zou; Ichiro Shiojima; Sumiyo Kudoh; Ruichi Aikawa; Dobun Hayashi; Miho Mizukami; Haruhiro Toko; Futoshi Shibasaki; Yoshio Yazaki; Ryozo Nagai; Issei Komuro
International Heart Journal | 2005
Tsuyoshi Taketani; Yasushi Imai; Tetsuro Morota; Koji Maemura; Hiroyuki Morita; Dobun Hayashi; Tsutomu Yamazaki; Ryozo Nagai; Shinichi Takamoto
Circulation | 2007
Takahide Kohro; Dobun Hayashi; Yoshihiro Okada; Tsutomu Yamazaki; Ryozo Nagai
Circulation | 2010
Takahide Kohro; Dobun Hayashi; Tsutomu Yamazaki; Ryozo Nagai
American Journal of Cardiology | 2007
Masatoshi Fujita; Tsutomu Yamazaki; Dobun Hayashi; Takahide Kohro; Yoshihiro Okada; Ryozo Nagai
Japanese Circulation Journal-english Edition | 2008
Kohro T; Dobun Hayashi; Okada Y; Tsutomu Yamazaki; Ryozo Nagai; Jcad Study Investigators
Circulation | 2005
Yasushi Imai; Tsuyoshi Taketani; Koji Maemura; Norihiko Takeda; Tomohiro Harada; Takefumi Nojiri; Daiji Kawanami; Koshiro Monzen; Dobun Hayashi; Yuji Murakawa; Minoru Ohno; Yoshinobu Hirata; Tsutomu Yamazaki; Shinichi Takamoto; Ryozo Nagai
Circulation | 2012
Katsumi Miyauchi; Tsutomu Yamazaki; Hirotaka Watada; Yasushi Tanaka; Ryuzo Kawamori; Yutaka Imai; Shunya Ikeda; Akira Kitagawa; Yasuhiro Ono; Fumio Murayama; Jong Bock Choi; Satoru Suwa; Dobun Hayashi; Junji Kishimoto; Hiroyuki Daida