Sukenari Koyabu
Mie University
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Featured researches published by Sukenari Koyabu.
Heart and Vessels | 2004
Tetsuya Nakakuki; Hiroshi Masuoka; Ken Ishikura; Tetsuya Seko; Sukenari Koyabu; Takuya Tamai; Masahiro Sugawa; Masaaki Ito; Takeshi Nakano
Primary cardiac lymphoma is a rare disorder with a poor prognosis. We present here a case of 77-year-old woman who was diagnosed as having cardiac lymphoma antemortem according to a cytologic examination of the pericardial effusion. Determination of the levels of serum-soluble interleukin-2 receptor and serum deoxythymidine kinase was useful for the diagnosis. Echocardiography, computed tomography, magnetic resonance imaging, and gallium scan revealed neither lymphadenopathy nor tumor in the heart, so she was diagnosed as having malignant lymphoma that probably originated from the pericardium. Systemic chemotherapy with CHOP (cyclophosphamide, farmorubicin, oncovin, and prednisolone) resulted in a complete resolution of the pericardial effusion. She has been in remission 48 months after discontinuation of the chemotherapy.
Pathology | 2003
Hiroya Kato; Sukenari Koyabu; Shigenori Aoki; Takuya Tamai; Masahiro Sugawa; Masatoshi Watanabe; Taizo Shiraishi
Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive lipid-storage disorder characterised by xanthomas, neurological dysfunctions and premature atherosclerosis. A case of a well differentiated adenocarcinoma of the gallbladder occurring in a 57-year-old Japanese man with CTX, confirmed clinically, biochemically and at autopsy is reported together with analyses of the sterol 27-hydroxylase (CYP27) and p53 genes. A missense mutation of the p53 (G for C) was detected in the gallbladder adenocarcinoma. Direct sequence analysis also showed a silent mutational substitution of unknown significance, C for A, in CYP27 at codon 89. In the past, CTX patients have only demonstrated this infrequently, indicating no direct relationship between CYP27 dysfunction and tumour development. Thus, the present case of gallbladder cancer appears to be a chance occurrence.
Pathology | 2003
Hiroya Kato; Sukenari Koyabu; Shigenori Aoki; Takuya Tamai; Masahiro Sugawa; Masatoshi Watanabe; Taizo Shiraishi
&NA; Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive lipid‐storage disorder characterised by xanthomas, neurological dysfunctions and premature atherosclerosis. A case of a well differentiated adenocarcinoma of the gallbladder occurring in a 57‐year‐old Japanese man with CTX, confirmed clinically, biochemically and at autopsy is reported together with analyses of the sterol 27‐hydroxylase (CYP27) and p53 genes. A missense mutation of the p53 (G for C) was detected in the gallbladder adenocarcinoma. Direct sequence analysis also showed a silent mutational substitution of unknown significance, C for A, in CYP27 at codon 89. In the past, CTX patients have only demonstrated this infrequently, indicating no direct relationship between CYP27 dysfunction and tumour development. Thus, the present case of gallbladder cancer appears to be a chance occurrence.
Clinical and Experimental Hypertension | 2018
Takayasu Ito; Naoki Fujimoto; Eiji Ishikawa; Kaoru Dohi; Mika Fujimoto; Tomohiro Murata; Michiyo Kiyohara; Hideyuki Takeuchi; Sukenari Koyabu; Hiroyuki Nishimura; Toshiaki Takeuchi; Masaaki Ito
ABSTRACT Background: Intradialytic hypertension (HTN), which is one of the poor prognostic markers in patients undergoing hemodialysis, may be associated with sympathetic overactivity. The L/N-type calcium channel blocker, cilnidipine, has been reported to suppress sympathetic nerves activity in vivo. Therefore, we hypothesized that cilnidipine could attenuate intradialytic systolic blood pressure (SBP) elevation. Methods: Fifty-one patients on chronic hemodialysis who had intradialytic-HTN (SBP elevation ≥10 mmHg during hemodialysis) and no fluid overload were prospectively randomized into two groups: control and cilnidipine groups. Cilnidipine group patients took cilnidipine (10 mg/day) for 12 weeks. The primary endpoint was the change in the intradialytic SBP elevation before and after the 12-week intervention. Results: Before the intervention, no differences were observed in age, sex or pre-dialytic SBP (148.5 ± 12.9 vs. 148.3 ± 19.3 mmHg) between the two groups. Intradialytic SBP elevation was unchanged in the control group. Cilnidipine significantly lowered the post-dialytic SBP with an attenuation of the intradialytic SBP elevation from 12.0 ± 15.4 mmHg to 4.8 ± 10.1 mmHg. However, the observed difference in the intradialytic SBP elevation by cilnidipine did not reach statistical significance (group×time interaction effect p = 0.25). Cathecolamine levels were unaffected by the intervention in both groups. Conclusion: Cilnidipine lowers both the pre- and post-dialytic SBP and might attenuate intradialytic SBP elevation. Therefore, cilnidipine may be effective in lowering SBP during HD in patients with intradialytic-HTN.
Journal of Clinical Hypertension | 2017
Toshiki Sawai; Kaoru Dohi; Naoki Fujimoto; Setsuya Okubo; Naoki Isaka; Takehiko Ichikawa; Katsutoshi Makino; Shinya Okamoto; Sukenari Koyabu; Tetsuya Kitamura; Toru Ogura; Tomomi Yamada; Satoshi Tamaru; Masakatsu Nishikawa; Mashio Nakamura; Masaaki Ito
This study investigated the effects and safety of eplerenone or thiazide diuretics in patients with hypertension and albuminuria (pretreatment urinary albumin/creatinine ratio ≥10 mg/gCr) treated with an angiotensin II receptor blocker. The primary end point was the mean percent change in the urinary albumin/creatinine ratio from baseline to 48 weeks. An efficacy analysis was performed in 195 patients (98 in the eplerenone group and 97 in the thiazide group). Systolic and diastolic blood pressures at 48 weeks were similar in the two groups. The mean percent change in the urinary albumin/creatinine ratio from baseline to 48 weeks was similar in the two groups (P=.804). In the safety analysis, the withdrawal rates for adverse events were similar in both groups. The antialbuminuric effects and safety of eplerenone therapy were similar to those of thiazide diuretics when combined with an angiotensin II receptor blocker in patients with hypertension and albuminuria.
Circulation | 2017
Hiroshi Matsuo; Kaoru Dohi; Hirofumi Machida; Hideyuki Takeuchi; Toshikazu Aoki; Hiroyuki Nishimura; Masashi Yasutomi; Michiharu Senga; Takehiko Ichikawa; Kentaro Kakuta; Yasuhide Mizutani; Akiko Tanoue; Naoki Isaka; Kazuki Oosugi; Sukenari Koyabu; Masato Sakurai; Yoshihisa Fukui; Hitoshi Kakimoto; Tadafumi Sugimoto; Takahiro Ohnishi; Tomohiro Murata; Eiji Ishikawa; Ryuji Okamoto; Tomomi Yamada; Toru Ogura; Yuki Nishimura; Takashi Tanigawa; Shinsuke Nomura; Masakatsu Nishikawa; Masaaki Ito
BACKGROUND The aim of this study was to assess the echocardiographic characteristics of chronic hemodialysis (HD) patients with end-stage renal disease (ESRD) in a multicenter prospective cohort study.Methods and Results:Three hundred and fifteen patients with ESRD (67.9±10.6 years, 47.6% male) on chronic HD for ≥1 year were examined on transthoracic echocardiography, including Doppler-derived aortic valve area (AVA) measurement. Only 11.5% and 3.4% of all patients had normal left ventricular (LV) geometry and normal LV filling pattern, respectively. The majority of patients had aortic and mitral valvular calcification, and approximately 50% of all 315 patients had aortic valve narrowing with AVA <2.0 cm2. Patients were divided into 3 groups according to AVA index tertile: group 1, highest tertile; group 2, middle tertile; and group 3, lowest tertile. Group 3 was older, had a greater cardiothoracic ratio on chest X-ray, higher plasma brain natriuretic peptide and total LV afterload, and lower stroke volume index than the other 2 groups. Age and intact parathyroid hormone (PTH) level were independently associated with low AVA index. CONCLUSIONS Patients with ESRD on chronic HD have a high prevalence of cardiac structural and functional abnormalities including calcified aortic sclerosis. High age and PTH were associated with aortic valve narrowing in these patients.
Internal Medicine | 1998
Hiroshi Okano; Hiroshi Masuoka; Shigeru Kamei; Tetsuya Seko; Sukenari Koyabu; Katsunobu Tsuneoka; Takuya Tamai; Kunihiko Ueda; Shigeo Nakazawa; Masahiro Sugawa; Hideo Suzuki; Masatoshi Watanabe; Ryuichi Yatani; Takeshi Nakano
Journal of Molecular and Cellular Cardiology | 1996
Kyoko Imanaka-Yoshida; Asaka Amitani; Sérgio O. Ioshii; Sukenari Koyabu; Tetsu Yamakado; Toshimichi Yoshida
Chest | 1993
Sukenari Koyabu; Naoki Isaka; Takashi Yada; Tokuji Konishi; Takeshi Nakano
American Heart Journal | 1998
Hiroshi Masuoka; Ken Ishikura; Shigeru Kamei; Toshihide Obe; Tetsuya Seko; Kazuaki Okuda; Sukenari Koyabu; Katsunobu Tsuneoka; Takuya Tamai; Masahiro Sugawa; Takeshi Nakano