研究者業績

大宮 直木

オオミヤ ナオキ  (Naoki Ohmiya)

基本情報

所属
藤田医科大学 医学部 医学科 先端光学診療学講座
学位
博士(医学)

J-GLOBAL ID
200901011108502975
researchmap会員ID
6000005568

患者さんの立場にたって、安全かつ最高の医療を提供できるよう努力します。

論文

 270
  • Takako Tsukamoto, Yohei Iwata, Naoki Ohmiya, Kazumitu Sugiura
    The Journal of dermatology 2024年9月30日  査読有り
  • Edouard Louis, Stefan Schreiber, Remo Panaccione, Peter Bossuyt, Luc Biedermann, Jean-Frederic Colombel, Gareth Parkes, Laurent Peyrin-Biroulet, Geert D’Haens, Tadakazu Hisamatsu, Britta Siegmund, Kaichun Wu, Brigid S. Boland, Gil Y. Melmed, Alessandro Armuzzi, Phillip Levine, Jasmina Kalabic, Su Chen, Ling Cheng, Lei Shu, W. Rachel Duan, Valerie Pivorunas, Yuri Sanchez Gonzalez, Ronilda D’Cunha, Ezequiel Neimark, Kori Wallace, Raja Atreya, Marc Ferrante, Edward V. Loftus, Domingo Balderramo, Silvina Goncalves, Juan Lasa, Abel Novillo, Orlando Ruffinengo, Sonja Heeren, Walter Reinisch, Filip Baert, Peter Bossuyt, Arnaud Colard, Olivier Dewit, Marc Ferrante, Denis Franchimont, Edouard Louis, Jean-Francois Rahier, Carlos Francesconi, Roberto Kaiser Junior, Rogerio Parra, Ligia Sassaki, Plamen Penchev, Desislav Stanchev, Kenneth Atkinson, Melanie Beaton, Talat Bessissow, Susan Greenbloom, Jean-Rene Lachance, Allen Lim, Remo Panaccione, Jean- Michel Samson, Scott Shulman, Jesse Siffledeen, Ignacio Alfaro, Carlos Valenzuela, Gustavo Walsen, Ping An, Qian Cao, Yan Chen, Youxiang Chen, Xiang Gao, Xiaohua Hou, Naizhong Hu, YAN Li, Fei Liu, Mei Liu, Lu Lungen, Zhihua Ran, Tongyu Tang, Xin Wang, Shaoqi Yang, Qiang Zhan, Guoxin Zhang, Hu Zhang, Jie Zhang, Xiaolan Zhang, Jie Zhong, Xiaoping Zou, Eligio Alvarez, Juan Ricaurte, Vladimir Borzan, Zeljko Krznaric, Zeljko Puljiz, Martin Bortlik, Pavel Svoboda, Jan Ulbrych, Tomas Vanasek, Jens Kjeldsen, Lars Munck, Anja Poulsen, Ezzat Ali, Osama Salem, Hisham Sawah, Imam Waked, Romain Altwegg, Mathurin FLAMANT, Mathurin Fumery, Xavier Hebuterne, David Laharie, Laurent Peyrin-Biroulet, Xavier Roblin, Xavier Treton, Raja Atreya, Herbert Deppe, Peter Hasselblatt, Arne Kandulski, Jochen Klaus, Thomas Krause, Torsten Kucharzik, Jessica Mertens, Michael Mross, Axel Naumann, Wolfgang Reindl, Ingolf Schiefke, Stefan Schreiber, Stefan Schubert, Britta Siegmund, Andreas Sturm, Georgios Bamias, Ioannis Koutroubakis, Spilios Manolakopoulos, Gerassimos Mantzaris, Maria Tzouvala, Irit Avni-Biron, Eran Goldin, Lior Katz, Adi Lahat-Zok, Arik Segal, Sandro Ardizzone, Alessandro Armuzzi, Michele Cicala, Antonio Colecchia, Rocco Cosintino, Antonio Gasbarrini, Andrea Geccherle, Edoardo Giovanni Giannini, Paolo Gionchetti, Francesco Luzza, Giovanni Monteleone, Antonino Privitera, Simone Saibeni, Marcello Vangeli, Yasuhiko Abe, Nobuo Aoyama, Kunio Asonuma, Yutaka Endo, Motohiro Esaki, Toshimitsu Fujii, Katsuyuki Fukuda, Fumihito Hirai, Yasuhiro Hisanaga, Noriyuki Horiki, Mikitaka Iguchi, Keisuke Ishigami, Yoh Ishiguro, Hiroaki Ito, Yoichi Kakuta, Koji Kamikozuru, Jun Kato, Teruki Kawanishi, Taku Kobayashi, Hiroyuki Kuge, Atsuo Maemoto, Tomoyuki Masuda, Katsuyoshi Matsuoka, Kayoko Matsushima, Masashi Matsushima, Satoshi Motoya, Katsuhiko Nakai, Koichi Nakajima, Masanao Nakamura, Atsushi Nishida, Takahiro Nishikawa, Nobuaki Nishimata, Toshiaki Ochiai, Naoki Ohmiya, Yoshifumi Ohnishi, Shiro Oka, Keiji Ozeki, Daisuke Saito, Masayuki Saruta, Makoto Sasaki, Masahito Shimizu, Ken Sugimoto, Tomohisa Sujino, Takayoshi Suzuki, Hajime Takatori, Noritaka Takatsu, Hidetoshi Takedatsu, Ken Takeuchi, Hiroki Tanaka, Satoki Tokito, Tatsuya Toyokawa, Yoshito Uenoyama, Takatsugu Yamamoto, Takayuki Yamamoto, Hiroshi Yasuda, Kaoru Yokoyama, Aleksejs Derovs, Aldis Pukitis, Laimas Jonaitis, Edita Kazenaite, Lourdes Lol-be Pinzon Te, Geert D'Haens, Maurice Lutgens, James Brooker, Richard Gearry, Ben Griffiths, Stephen Inns, Michael Schultz, Jerzy Eszyk, Jaroslaw Kierkus, Dariusz Kleczkowski, Adam Kopon, Robert Petryka, Jaroslaw Regula, Tomasz Romanczyk, Grazyna Rydzewska-Wyszkowska, Piotr Sikorski, Michal Talarek, Rute Cerqueira, Tiago Goncalves, Susana Lopes, Paula Ministro, Francisco Portela, Helena Tavares, Mihai-Mircea Diculescu, Adrian Goldis, Andrada Seicean, Alina Agafina, Anton Edin, Evgenia Gerasimova, Maryana Gettueva, Vladimir Kashnikov, Vladimir Rafalskiy, Ksenia Sharapova, Elena Smolyarchuk, Daria Varganova, Sasa Grgov, Igor Jovanovic, Petar Svorcan, Dino Tarabar, Khoon Lin Ling, Jozef Balaz, Juraj Durina, Milos Gregus, Martin Laclav, David Drobne, Eduan Deetlefs, Jonny Peter, Muhammad Rajabally, Jennifer Rosa, Jan van Zyl, John Wright, Jae Hee Cheon, Byung Ik Jang, Sang-Bum Kang, Dukhwan Kim, Tae Oh Kim, Young-Ho Kim, Jonghun Lee, Kang-Moon Lee, Dong Il Park, Geun Am Song, Luisa Castro Laria, Ana Echarri Piudo, Santiago Garcia Lopez, Vincent Hernandez Ramirez, Maria Dolores Martin Arranz, Pilar Varela Trastoy, Maria Vera Mendoza, Mikael Lordal, Luc Biedermann, Benjamin Misselwitz, Chung-Hsin Chang, Jen-Wei Chou, Chia-Jung Kuo, Ching-Pin Lin, Chia-Hung Tu, Huseyin Alkim, Yusuf Erzin, Irfan Soykan, Tetiana Kravchenko, Nataliia Tsarynna, Vira Vyshyvanyuk, Tariq Ahmad, Fraser Cummings, Kapil Kapur, Arthur Kaser, Alexandra Kent, Gareth Parkes, Kamal Patel, Richard Speight, Alan Steel, Faten Aberra, Humberto Aguilar, Badr Al Bawardy, Ashwin Ananthakrishnan, Matthew Barnes, Kendall Beck, Charles Berkelhammer, Brigid Boland, Jeff Bullock, Adeeti Chiplunker, Robin Dalal, Sushila Dalal, Belkis Delgado, Michael DiGiovanna, George Aaron DuVall, Curtis Freedland, Keith Friedenberg, Philip Ginsburg, Tarek Hassanein, Peter Higgins, John Hong, Jason Hou, Vivek Huilgol, Nikhil Inamdar, Saurabh Kapur, David Kerman, Henry Levine, Nilesh Lodhia, Edward Loftus, Jaime Mayoral, Donald McNeil, Gil Melmed, Andria Mushahwar, Harry Ojeas, Bhaktasharan Patel, Raymond Phillips, Joe Pouzar, Harry Sarles Jr., Joel Schock, Shahriar Sedghi, Nirav Shah, Junaid Siddiqui, David Stokesberry, Le-Chu Su, Arun Swaminath, Dharmendra Verma, John Weber, Ziad Younes, Timothy Zisman
    JAMA 2024年7月22日  査読有り
    Importance The clinical effects of risankizumab (a monoclonal antibody that selectively targets the p19 subunit of IL-23) for the treatment of ulcerative colitis are unknown. Objective To evaluate the efficacy and safety of risankizumab when administered as an induction and a maintenance therapy for patients with ulcerative colitis. Design, Setting, and Participants Two phase 3 randomized clinical trials were conducted. The induction trial was conducted at 261 clinical centers (in 41 countries) and enrolled 977 patients from November 5, 2020, to August 4, 2022 (final follow-up on May 16, 2023). The maintenance trial was conducted at 238 clinical centers (in 37 countries) and enrolled 754 patients from August 28, 2018, to March 30, 2022 (final follow-up on April 11, 2023). Eligible patients had moderately to severely active ulcerative colitis; a history of intolerance or inadequate response to 1 or more conventional therapies, advanced therapies, or both types of therapies; and no prior exposure to risankizumab. Interventions For the induction trial, patients were randomized 2:1 to receive 1200 mg of risankizumab or placebo administered intravenously at weeks 0, 4, and 8. For the maintenance trial, patients with a clinical response (determined using the adapted Mayo score) after intravenous treatment with risankizumab were randomized 1:1:1 to receive subcutaneous treatment with 180 mg or 360 mg of risankizumab or placebo (no longer receiving risankizumab) every 8 weeks for 52 weeks. Main Outcomes and Measures The primary outcome was clinical remission (stool frequency score ≤1 and not greater than baseline, rectal bleeding score of 0, and endoscopic subscore ≤1 without friability) at week 12 for the induction trial and at week 52 for the maintenance trial. Results Among the 975 patients analyzed in the induction trial (aged 42.1 [SD, 13.8] years; 586/973 [60.1%] were male; and 677 [69.6%] were White), the clinical remission rates at week 12 were 132/650 (20.3%) for 1200 mg of risankizumab and 20/325 (6.2%) for placebo (adjusted between-group difference, 14.0% [95% CI, 10.0%-18.0%], P < .001). Among the 548 patients analyzed in the maintenance trial (aged 40.9 [SD, 14.0] years; 313 [57.1%] were male; and 407 [74.3%] were White), the clinical remission rates at week 52 were 72/179 (40.2%) for 180 mg of risankizumab, 70/186 (37.6%) for 360 mg of risankizumab, and 46/183 (25.1%) for placebo (adjusted between-group difference for 180 mg of risankizumab vs placebo, 16.3% [97.5% CI, 6.1%-26.6%], P < .001; adjusted between-group difference for 360 mg of risankizumab vs placebo, 14.2% [97.5% CI, 4.0%-24.5%], P = .002). No adverse event signals were detected in the treatment groups. Conclusion and Relevance Compared with placebo, risankizumab improved clinical remission rates in an induction trial and in a maintenance trial for patients with moderately to severely active ulcerative colitis. Further study is needed to identify benefits beyond the 52-week follow-up. Trial Registration ClinicalTrials.gov Identifiers: NCT03398148 and NCT03398135
  • Tomomitsu Tahara, Noriyuki Horiguchi, Hyuga Yamada, Tsuyoshi Terada, Dai Yoshida, Masaaki Okubo, Kohei Funasaka, Yoshihito Nakagawa, Tomoyuki Shibata, Naoki Ohmiya
    Journal of gastrointestinal and liver diseases : JGLD 33(2) 164-169 2024年6月29日  査読有り
    BACKGROUND AND AIMS: Early gastric cancers (EGCs) after Helicobacter pylori (H. pylori) eradication often appear as reddish depressed lesions (RDLs); the same features are also appeared in benign stomachs after eradication. We compared clinic-pathological and endoscopic features of benign and neoplastic RDLs after H. pylori eradication. METHODS: 228 neoplastic RDLs after H. pylori eradication were studied. All lesions were divided into neoplastic RDLs (differentiated carcinoma or adenoma, n=114) and benign RDLs (n=114) according to the histology. Clinical and pathological characteristics were compared in neoplastic and benign groups. Endoscopic diagnostic yields using the white light (WL) endoscopy, chromoendoscopy (CE) using indigo carmine dye and the magnifying endoscopy with narrow-band imaging (ME-NBI) were also evaluated in relation to the pathological diagnosis. RESULTS: Size of neoplastic RDLs was larger than that of benign RDLs (p<0.01). Sensitivity, specificity and accuracy for predicting pathological types of RDLs was 70.1%, 52.6% and 61.4% for the WL, 65.8%, 63.1% and 65.4% for the CE, while the ME-NBI scored better with the 88.6%, 88.6%, 99.1% and 93.9% of sensitivity, specificity and accuracy. The accuracy of the ME-NBI was 99.9% (113/114) in the benign RDLs and 89.4% (101/114) for the neoplastic RDLs. Undiagnosed neoplastic RDLs using the ME-NBI were associated with more differentiated tumors such as adenoma and well-differentiated adenocarcinoma (tub1) and the presence of an unclear demarcation line. CONCLUSIONS: ME-NBI is useful to diagnose RDLs after H. pylori eradiation, while some of neoplastic lesions are difficult to diagnose using the ME-NBI.
  • Ken Yamashita, Shiro Oka, Takeshi Yamada, Keigo Mitsui, Hironori Yamamoto, Keiichi Takahashi, Akio Shiomi, Kinichi Hotta, Yoji Takeuchi, Toshio Kuwai, Fumio Ishida, Shin-Ei Kudo, Shoichi Saito, Masashi Ueno, Eiji Sunami, Tomoki Yamano, Michio Itabashi, Kazuo Ohtsuka, Yusuke Kinugasa, Takayuki Matsumoto, Tamotsu Sugai, Toshio Uraoka, Koichi Kurahara, Shigeki Yamaguchi, Tomohiro Kato, Masazumi Okajima, Hiroshi Kashida, Yoshito Akagi, Hiroaki Ikematsu, Masaaki Ito, Motohiro Esaki, Masaya Kawai, Takashi Yao, Madoka Hamada, Takahiro Horimatsu, Keiji Koda, Yasumori Fukai, Koji Komori, Yusuke Saitoh, Yukihide Kanemitsu, Hiroyuki Takamaru, Kazutaka Yamada, Hiroaki Nozawa, Tetsuji Takayama, Kazutomo Togashi, Eiji Shinto, Takehiro Torisu, Akira Toyoshima, Naoki Ohmiya, Takeshi Kato, Eigo Otsuji, Shinji Nagata, Yojiro Hashiguchi, Kenichi Sugihara, Yoichi Ajioka, Shinji Tanaka
    Journal of gastroenterology 59(5) 376-388 2024年5月  査読有り
    BACKGROUND: The clinicopathological features and prognosis of primary small bowel adenocarcinoma (PSBA), excluding duodenal cancer, remain undetermined due to its rarity in Japan. METHODS: We analyzed 354 patients with 358 PSBAs, between January 2008 and December 2017, at 44 institutions affiliated with the Japanese Society for Cancer of the Colon and Rectum. RESULTS: The median age was 67 years (218 males, 61.6%). The average tumor size was 49.9 (7-100) mm. PSBA sites consisted of jejunum (66.2%) and ileum (30.4%). A total of 219 patients (61.9%) underwent diagnostic small bowel endoscopy, including single-balloon endoscopy, double-balloon endoscopy, and capsule endoscopy before treatment. Nineteen patients (5.4%) had Lynch syndrome, and 272 patients (76.8%) had symptoms at the initial diagnosis. The rates for stages 0, I, II, III, and IV were 5.4%, 2.5%, 27.1%, 26.0%, and 35.6%, respectively. The 5-year overall survival rates at each stage were 92.3%, 60.0%, 75.9%, 61.4%, and 25.5%, respectively, and the 5-year disease-specific survival (DSS) rates were 100%, 75.0%, 84.1%, 59.3%, and 25.6%, respectively. Patients with the PSBA located in the jejunum, with symptoms at the initial diagnosis or advanced clinical stage had a worse prognosis. However, multivariate analysis using Cox-hazard model revealed that clinical stage was the only significant predictor of DSS for patients with PSBA. CONCLUSIONS: Of the patients with PSBA, 76.8% had symptoms at the initial diagnosis, which were often detected at an advanced stage. Detection during the early stages of PSBA is important to ensure a good prognosis.
  • 堀口 徳之, 大宮 直木, 舩坂 好平, 長坂 光夫, 大野 栄三郎, 中川 義仁, 葛谷 貞二, 宮原 良二, 柴田 知行, 廣岡 芳樹
    日本消化器病学会雑誌 121(臨増総会) A190-A190 2024年3月  

MISC

 1258
  • Takayoshi Fujita, Takafumi Ando, Osamu Watanabe, Motofusa Hasegawa, Nobuyuki Miyake, Shinya Kondo, Tsuyoshi Kato, Kazuhiro Ishiguro, Masanao Nakamura, Ryoji Miyahara, Naoki Ohmiya, Yasumasa Niwa, Hidemi Goto
    HEPATO-GASTROENTEROLOGY 57(99-100) 487-492 2010年5月  査読有り
    Background/Aims: Colorectal cancer (CRC) was first recognized as a complication of ulcerative colitis (UC) in 1925, and the increased risk has since been confirmed in a multitude of epidemiological studies. To our knowledge, however, all of these studies have been conducted in Western countries. The aim of this study was to identify the clinicopathological features of ulcerative colitis-related CRC in a consecutive series of patients at a single hospital in central Japan. Methodology: 314 (170 males, 144 females, mean age 30) consecutive patients diagnosed with ulcerative colitis were enrolled and investigated for the development of CRC. 240 patients had relapsing-remitting disease, 54 had chronic continuous disease, 16 had experienced one attack only, 2 had the acute fulminating type, and 2 were unknown. With regard to disease extension, 181 cases were of the pan-colitis type, 84 were left-sided colitis, and 42 were proctitis. Two patients (1%) had a family history of colorectal cancer and 45 (14%) were past or current smokers. Results: Colorectal cancer developed in seven patients (male to female ratio of 1:6), which was 2.2% of the total. Average age at the onset of ulcerative colitis was 28 years. Average age at the onset of cancer was 44 years, and average duration of UC at cancer onset was 192 months. Ulcerative colitis was of the pancolitis type in all cases. Three patients (43%) showed the relapse-remitting type and four (57%) the chronic continuing type. Three patients (43%) had a family history of cancer, in particular colorectal cancer in one patient (14%). None of the patients had a history of smoking. The histological type of cancer was well differentiated tubular adenocarcinoma in three patients (43%) and poorly differentiated adenocarcinoma in three patients (43%) each, and endocrine cell carcinoma in one (14%). Conclusions: In this group of Japanese patients, development of colorectal cancer was more likely to occur in patients with ulcerative colitis that was long-standing, and more extensive than left-sided colitis, particularly in those with a family history of colorectal cancer, inflammatory polyps, or dysplasia. CRCs in our patients with UC were often poorly differentiated and had a poor prognosis.
  • Koji Nonogaki, Akihiro Itoh, Hiroki Kawashima, Eizaburo Ohno, Takuya Ishikawa, Hiroshi Matsubara, Yuya Itoh, Yosuke Nakamura, Masanao Nakamura, Ryoji Miyahara, Naoki Ohmiya, Masatoshi Ishigami, Yoshiaki Katano, Hidemi Goto, Yoshiki Hirooka
    Journal of experimental & clinical cancer research : CR 29 36-36 2010年4月25日  査読有り
    Background: Analysis of gene expression and gene mutation may add information to be different from ordinary pathological tissue diagnosis. Since samples obtained endoscopically are very small, it is desired that more sensitive technology is developed for gene analysis. We investigated whether gene expression and gene mutation analysis by newly developed ultra-sensitive three-dimensional (3D) microarray is possible using small amount samples from endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) specimens and pancreatic juices. Methods: Small amount samples from 17 EUS-FNA specimens and 16 pancreatic juices were obtained. After nucleic acid extraction, the samples were amplified with labeling and analyzed by the 3D microarray. Results: The analyzable rate with the microarray was 46% (6/13) in EUS-FNA specimens of RNAlater (R) storage, and RNA degradations were observed in all the samples of frozen storage. In pancreatic juices, the analyzable rate was 67% (4/6) in frozen storage samples and 20% (2/10) in RNAlater (R) storage. EUS-FNA specimens were classified into cancer and non-cancer by gene expression analysis and K-ras codon 12 mutations were also detected using the 3D microarray. Conclusions: Gene analysis from small amount samples obtained endoscopically was possible by newly developed 3D microarray technology. High quality RNA from EUS-FNA samples were obtained and remained in good condition only using RNA stabilizer. In contrast, high quality RNA from pancreatic juice samples were obtained only in frozen storage without RNA stabilizer.
  • Takafumi Ando, Kazuhiro Ishiguro, Osamu Maeda, Osamu Watanabe, Nobuyuki Miyake, Masanao Nakamura, Ryoji Miyahara, Naoki Ohmiya, Hidemi Goto
    GASTROINTESTINAL ENDOSCOPY 71(5) AB345-AB346 2010年4月  
  • Yoshiki Hirooka, Akihiro Itoh, Hiroki Kawashima, Eizaburo Ohno, Takuya Ishikawa, Hiroshi Matsubara, Yuya Itoh, Yosuke Nakamura, Masanao Nakamura, Ryoji Miyahara, Naoki Ohmiya, Masatoshi Ishigami, Yoshiaki Katano, Hidemi Goto
    GASTROINTESTINAL ENDOSCOPY 71(5) AB275-AB275 2010年4月  
  • Hiroyuki Takenaka, Naoki Ohmiya, Masanao Nakamura, Kenji Morishima, Ryoji Miyahara, Hiroki Kawashima, Akihiro Itoh, Yoshiki Hirooka, Osamu Watanabe, Takafumi Ando, Hidemi Goto
    GASTROINTESTINAL ENDOSCOPY 71(5) AB372-AB372 2010年4月  
  • Ryogi Miyahara, Yoshiki Hirooka, Toshikio Nagaya, Kakunori Banno, Masanao Nakamura, Hiroki Kawashima, Akihiro Itoh, Naoki Ohmiya, Osamu Watanabe, Osamu Maeda, Takafumi Ando, Hidemi Goto
    GASTROINTESTINAL ENDOSCOPY 71(5) AB294-AB294 2010年4月  
  • Naoki Ohmiya, Masanao Nakamura, Hiroyuki Takenaka, Kenji Morishima, Takeshi Yamamura, Makoto Ishihara, Ryoji Miyahara, Hiroki Kawashima, Akihiro Itoh, Yoshiki Hirooka, Osamu Watanabe, Takafumi Ando, Hidemi Goto
    GASTROINTESTINAL ENDOSCOPY 71(5) AB373-AB374 2010年4月  
  • Takuya Ishikawa, Yoshiki Hirooka, Akihiro Itoh, Hiroki Kawashima, Eizaburo Ohno, Hiroshi Matsubara, Yuya Itoh, Yosuke Nakamura, Masanao Nakamura, Ryoji Miyahara, Naoki Ohmiya, Hidemi Goto
    GASTROINTESTINAL ENDOSCOPY 71(5) AB279-AB279 2010年4月  
  • Masanao Nakamura, Naoki Ohmiya, Hiroyuki Takenaka, Kenji Morishima, Makoto Ishihara, Ryoji Miyahara, Takafumi Ando, Osamu Watanabe, Hiroki Kawashima, Akihiro Itoh, Yoshiki Hirooka, Hidemi Goto
    GASTROINTESTINAL ENDOSCOPY 71(5) AB270-AB270 2010年4月  
  • Kakunori Banno, Ryoji Miyahara, Toshihiko Nagaya, Masanao Nakamura, Hiroki Kawashima, Akihiro Itoh, Naoki Ohmiya, Yoshiki Hirooka, Osamu Watanabe, Osamu Maeda, Takafumi Ando, Hidemi Goto
    GASTROINTESTINAL ENDOSCOPY 71(5) AB181-AB182 2010年4月  
  • 廣岡 芳樹, 伊藤 彰浩, 川嶋 啓揮, 中村 正直, 宮原 良二, 大宮 直木, 林 和彦, 片野 義明, 後藤 秀実
    超音波医学 37(Suppl.) S255-S255 2010年4月  
  • 中村 正直, 大宮 直木, 後藤 秀実
    Gastroenterological Endoscopy 52(Suppl.1) 786-786 2010年4月  
  • 竹中 宏之, 大宮 直木, 後藤 秀実
    Gastroenterological Endoscopy 52(Suppl.1) 800-800 2010年4月  
  • 森島 賢治, 大宮 直木, 後藤 秀実
    Gastroenterological Endoscopy 52(Suppl.1) 862-862 2010年4月  
  • 渡辺 修, 安藤 貴文, 石黒 和博, 前田 修, 三宅 忍幸, 加藤 剛, 日比 知志, 神谷 徹, 三村 俊哉, 中村 正直, 宮原 良二, 大宮 直木, 後藤 秀実
    Gastroenterological Endoscopy 52(Suppl.1) 957-957 2010年4月  
  • 三宅 忍幸, 安藤 貴文, 石黒 和博, 前田 修, 渡辺 修, 加藤 剛, 日比 知志, 神谷 徹, 三村 俊哉, 中村 正直, 宮原 良二, 大宮 直木, 後藤 秀実
    Gastroenterological Endoscopy 52(Suppl.1) 977-977 2010年4月  
  • 坂巻 慶一, 宮原 良二, 長屋 寿彦, 坂野 閣紀, 古川 和宏, 立松 英純, 中村 正直, 川嶋 啓揮, 伊藤 彰浩, 大宮 直木, 廣岡 芳樹, 渡辺 修, 前田 修, 安藤 貴文, 後藤 秀実, 丹羽 康正
    Gastroenterological Endoscopy 52(Suppl.1) 994-994 2010年4月  
  • 中村 陽介, 廣岡 芳樹, 伊藤 彰浩, 川嶋 啓揮, 大野 栄三郎, 石川 卓哉, 松原 浩, 伊藤 裕也, 中村 正直, 宮原 良二, 大宮 直木, 後藤 秀実
    Gastroenterological Endoscopy 52(Suppl.1) 1051-1051 2010年4月  
  • Hidemi Goto, Masanao Nakamura, Naoki Ohmiya, Yoshiki Hirooka, Akihiro Itoh
    Journal of gastroenterology 45(4) 468-9 2010年4月  査読有り
  • Kakunori Banno, Yasumasa Niwa, Ryoji Miyahara, Masanao Nakamura, Toshihiko Nagaya, Tetsuro Nagasaka, Osamu Watanabe, Takafumi Ando, Hiroki Kawashima, Naoki Ohmiya, Akihiro Itoh, Yoshiki Hirooka, Hidemi Goto
    Journal of gastroenterology and hepatology 25(4) 712-8 2010年4月  査読有り
    Background and Aim: Relationships between mucin phenotype and malignant potential in gastric cancers have attracted attention. We attempted to assess the possibility of obtaining phenotypic diagnoses by confocal endomicroscopy. Methods: Confocal images of target lesions were obtained in 29 of 40 patients with gastric cancer. Appearances of the brush border, goblet cells, and gastric foveolar epithelium were investigated with immunohistochemical staining using CD10, MUC2, and human gastric mucin to evaluate phenotypic expression in gastric carcinomas. Confocal images were compared with immunohistochemical findings for goblet cells and brush borders. Results: Both the endoscopists and the pathologist obtained high accuracy rates for differential diagnosis. Sensitivity and specificity for goblet cells were 85.7% and 92.3% (Endoscopist A), and 85.7% and 88.5% (Endoscopist B). The kappa-value for correspondence between two endoscopists for the diagnosis of goblet cells in confocal images was 0.73. Sensitivity and specificity for the brush border were 93.8% and 91.7% (Endoscopist A), and 81.3% and 91.7% (Endoscopist B). The kappa-value for correspondence between two endoscopists for diagnosis of the brush border in confocal images was 0.79. Intestinal phenotypic gastric cancers show a brush border, goblet cells, or both. Sensitivity and specificity for the intestinal phenotype in confocal endomicroscopy were 90.9% and 77.8% (Endoscopist A), and 86.4% and 83.3% (Endoscopist B). Conclusion: The confocal endomicroscopic diagnosis of the mucin phenotype in gastric cancers was limited to intestinal and mixed phenotypes, but may be useful for the diagnosis of mucin phenotype and differential diagnosis.
  • 大宮 直木, 中村 正直, 後藤 秀実
    日本消化器病学会雑誌 107(臨増総会) A152-A152 2010年3月  
  • 日比 知志, 安藤 貴文, 石黒 和博, 前田 修, 渡辺 修, 三宅 忍幸, 加藤 剛, 神谷 徹, 三村 俊哉, 中村 正直, 宮原 良二, 大宮 直木, 後藤 秀実
    日本消化器病学会雑誌 107(臨増総会) A216-A216 2010年3月  
  • 渡辺 修, 安藤 貴文, 石黒 和博, 前田 修, 三宅 忍幸, 加藤 剛, 日比 知志, 神谷 徹, 三村 俊哉, 中村 正直, 宮原 良二, 大宮 直木, 後藤 秀実
    日本消化器病学会雑誌 107(臨増総会) A324-A324 2010年3月  
  • 坂野 閣紀, 宮原 良二, 長屋 寿彦, 古川 和宏, 坂巻 慶一, 立松 英純, 中村 正直, 川嶋 啓揮, 伊藤 彰浩, 大宮 直木, 廣岡 芳樹, 渡辺 修, 前田 修, 安藤 貴文, 後藤 秀実
    日本消化器病学会雑誌 107(臨増総会) A346-A346 2010年3月  
  • 渡辺 修, 安藤 貴文, 石黒 和博, 前田 修, 三宅 忍幸, 加藤 剛, 日比 知志, 神谷 徹, 三村 俊哉, 中村 正直, 宮原 良二, 大宮 直木, 後藤 秀実
    消化器と免疫 (46) 180-183 2010年3月  
    酢酸は、腸管細菌叢が産生する短鎖脂肪酸の多くの部分を占め、炎症性腸疾患ではその産生量の減少が報告されている。我々はマウスの炎症疾患モデルに対して酢酸と同様の効果がある酢酸Naが抗炎症効果について報告してきた。今回、潰瘍性大腸炎患者4例およびクローン病患者1例に対して酢酸Na注腸を4週間施行した。全例で副作用なく施行でき、潰瘍性大腸炎患者4例中2例、クローン病患者1例で内視鏡所見や臨床症状の改善がみられた。(著者抄録)
  • 中村 亮一, 松本 慎二郎, 平山 正昭, 熱田 直樹, 渡辺 宏久, 祖父江 元, 森島 賢治, 大宮 直木, 後藤 秀実
    臨床神経学 50(2) 116-116 2010年2月  
  • 石原誠, 大宮直木, 中村正直, 後藤秀実
    THROMBOSIS and Circulation 18(3) 46(200)-49(203) 2010年  
    <§論文のポイント>[1]カプセル内視鏡やバルーン内視鏡の開発は小腸疾患に大きな変化をもたらした。[2]アスピリンは上部消化管だけでなく小腸粘膜障害を高率に引き起こす。[3]予防や治療に関してPG製剤、レバミピドなどの有用性が報告されているが、明らかなevidenceはない。(著者抄録)
  • 石原誠, 大宮直木, 中村正直, 後藤秀実
    THROMBOSIS and Circulation 18(3) 46(200)-49(203) 2010年  
  • 中村正直, 大宮直木, 後藤秀実
    G.I.Reseach 18(6) 18(498)-24(504) 2010年  
  • 鶴留一誠, 宮原良二, 舩坂好平, 坂野閣紀, 中村正直, 川嶋啓揮, 伊藤彰浩, 大宮直木, 廣岡芳樹, 後藤秀実
    消化器外科NURSING2010 15(9) 34-39 2010年  
  • 中村正直, 大宮直木, 荒川大吾, 本田亘, 丹羽康正, 後藤秀実
    臨牀消化器内科 21(10) 1409-1414 2010年  
  • 石川卓哉, 廣岡芳樹, 伊藤彰浩, 川嶋啓揮, 大野栄三郎, 松原浩, 伊藤裕也, 中村正直, 宮原良二, 大宮直木, 丹羽康正, 後藤秀実
    肝胆膵 60(1) 5-78 2010年  
  • 山村健史, 大宮直木, 中村正直, 竹中宏之, 森島賢治, 石原誠, 宮原良二, 渡辺修, 安藤貴文, 川嶋啓揮, 伊藤彰浩, 廣岡芳樹, 後藤秀実
    胃と腸 45(3) 355-362 2010年  
  • 川嶋啓揮, 廣岡芳樹, 伊藤彰浩, 大野栄三郎, 石川卓哉, 松原浩, 伊藤裕也, 中村陽介, 中村正直, 宮原良二, 大宮直木, 後藤秀実
    消化器内科 50(2) 180-183 2010年  
    術前に進展範囲診断目的で内視鏡的逆行性胆管造影(ERC)の手技を用いた経乳頭的胆管生検を施行し、最終的に胆管癌と診断された48例(男33例・女15例・平均67.7歳)について報告した。生検目的のERCは53回施行し、48例中14例で造影像よりも広範な癌の進展が証明された。肉眼的形態分類別にみると、結節型19例中9例、乳頭型13例中4例、平坦型16例中1例であった。術後膵炎は53回の検査後7回で認めたが、全例軽度で保存的に改善した。術後胆管炎は4回で認め、術前に内瘻によるドレナージが留置されていた症例に多かった。以上、経乳頭的胆管生検は胆管癌の術前診断として有用であると考えられた。
  • 中村正直, 大宮直木, 竹中宏之, 森島賢治, 石原誠, 宮原良二, 前田修, 渡辺修, 川嶋啓揮, 伊藤彰浩, 廣岡芳樹, 安藤貴文, 後藤秀実
    消化器内視鏡 22(33) 295-302 2010年  
  • 中村正直, 大宮直木, 竹中宏之, 森島賢治, 石原誠, 宮原良二, 渡辺修, 前田修, 川嶋啓揮, 伊藤彰浩, 廣岡芳樹, 安藤貴文, 丹羽康正, 後藤秀実
    消化器の臨床 13(2) 184-189 2010年  
    カプセル内視鏡が臨床導入され、非ステロイド系抗炎症薬(NSAID)による小腸粘膜傷害の存在が顕在化するようになってきた。我々は2004年よりカプセル内視鏡による小腸疾患の臨床研究に着手し、NSAID小腸粘膜傷害を比較的容易に観察できることを報告してきた。また、NSAID小腸粘膜傷害の予防に関する研究が必要と考えていた。そこで、ボランティアを用いレバミピドによるNSAID誘発小腸傷害予防試験を実施し、その有用性を確認した。(著者抄録)
  • 中村正直, 大宮直木, 後藤秀実
    消化器内視鏡4 22(4) 572-574 2010年  
  • 宮原良二, 廣岡芳樹, 舩坂好平, 坂野閣紀, 坂巻慶一, 立松英純, 鶴留一誠, 中村正直, 川嶋啓揮, 伊藤彰浩, 大宮直木, 後藤秀実
    消化器内視鏡 22(5) 813-819 2010年  
  • 森島賢治, 大宮直木, 後藤秀実
    診断と治療社 72-74 2010年  
  • 廣岡芳樹, 伊藤彰浩, 川嶋啓揮, 大野栄三郎, 石川卓哉, 松原浩, 伊藤裕也, 中村陽介, 平松武, 中村正直, 宮原良二, 大宮直木, 石上雅敏, 片野義明, 金子享, 後藤重則, 高原将司, 後藤秀実
    胆と膵 31(10) 1245-1248 2010年  
    膵癌は消化器癌のみならず、全ての悪性腫瘍の中で最も予後不良な腫瘍の一つである。現在、切除不能局所進行膵癌に対して化学放射線療法が有効であると考えられているが、十分な治療効果が得られているとは言い難く、新しい治療法の開発が求められている。そこで、われわれのチームでは、切除不能局所進行膵癌患者5例に対する一次治療として、標準化学療法剤であるゲムシタビン(GEM)と樹状細胞(DC)のEUSガイド下腫瘍内局所投与、およびCD3-LAK(Lymphokine-activated killer cells)静脈内投与を併用した臨床試験を実施した。その結果、グレード3以上の有害事象は認められず、PR(partial response)1例、6ヵ月間以上のSD(stable disease)2例、PD(progressive disease)2例と良好な結果が得られため、本稿では試験の方法論および結果について紹介する。(著者抄録)
  • 大宮直木, 中村正直, 竹中宏之, 森島賢治, 石原誠, 小原圭, 水谷太郎, 山村健史, 宮原良二, 川嶋啓揮, 伊藤彰浩, 廣岡芳樹, 渡辺修, 安藤貴文, 後藤秀実
    胃と腸 45(13) 2079-2084 2010年  
    Peutz-Jeghers症候群の小腸ポリープは腸重積,出血,腹痛の原因となるが,近年のカプセル内視鏡(VCE),ダブルバルーン内視鏡(DBE)の開発でその診断・治療は容易となった.小腸ポリープ数の比較試験では小腸X線と比較し,VCE,DBEの検出能は優れており,さらにVCEはDBEに比し全小腸観察率が高かった.DBE下小腸ポリープ摘除は有効かつ低侵襲であった.回収したポリープの病理学的検索では20mm以下のポリープの腺腫合併率は1%,20mmを超えるポリープの腺腫・腺癌の合併率は27%と有意差があった.小腸ポリープの増殖能を規定する因子は小腸,大腸ポリープ数であったことから,ポリープ摘除後のフォローアップは小腸,大腸ポリープ数を勘案して半年〜4年ごとにカプセル内視鏡で行うのがよいと思われた.(著者抄録)
  • 中村 正直, 大宮 直木, 宮原 良二, 安藤 貴文, 渡辺 修, 川嶋 啓揮, 伊藤 彰浩, 廣岡 芳樹, 丹羽 康正, 後藤 秀実
    Gastroenterological Endoscopy 51(11) 2866-2876 2009年11月  
    原因不明の消化管出血(OGIB)例におけるカプセル内視鏡(VCE)の診断的意義について検討した。対象は2004年11月〜2008年2月までにVCE、ダブルバルーン内視鏡(DBE)の順で精査を行ったOGIB例116例(男性70例、女性46例、平均年齢62.2歳)で、VCEの診断および所見をDBEや生検などの組織診断による最終診断と比較した。その結果、VCEの有所見率は73例(62.9%)であったが、VCEでOGIBの診断を得たのは20例(17.2%、内訳はangiodysplasia:17例、回腸癌、鉤虫症、動静脈奇形:各1例)であり、最終診断と一致したのは13例(11.2%、内訳はangiodysplasia:10例、回腸癌、鉤虫症、動静脈奇形:各1例)と低率であった。尚、VCEの感度は76.7%、特異度は74.2%で、陽性的中率は87.5%、陰性的中率は57.5%、正診率は76.0%であった。以上、VCEではOGIBと最終診断を得るのは少ないが、最終診断への有効な情報源として有用と考えられた。
  • Youichi Iguchi, Yasumasa Niwa, Ryoji Miyahara, Masanao Nakamura, Kakunori Banno, Toshihiko Nagaya, Tetsuro Nagasaka, Osamu Watanabe, Takafumi Ando, Hiroki Kawashima, Naoki Ohmiya, Akihiro Itoh, Yoshiki Hirooka, Hidemi Goto
    Journal of gastroenterology and hepatology 24(11) 1733-9 2009年11月  査読有り
    Background and Aim: Confocal endomicroscopy is ultra-high-magnification endoscopy with histological observation during ongoing endoscopy. We planned a pilot study of the diagnosis of the depth of esophageal cancer using confocal endomicroscopy for treatment strategies. Methods: Patients had 14 superficial esophageal cancers and one dysplasia. The depth of neoplasms in 15 lesions was confirmed by endoscopic mucosal resection or surgery. We examined the rate of delineation and compared results of confocal imaging with histological findings. We classified two cellular and three microvascular patterns on confocal endomicroscopic images: CP-N for normal squamous mucosa and CP-Ca for cancerous lesion; VP-type A for normal squamous mucosa; VP-type B for T1a-EP and T1a-LPM cancers; and VP-type C for T1a-MM or a more invasive cancer pattern. We measured diameters of microvessels for the three patterns of confocal endomicroscopic images and histological specimens. Results: The rate of delineation was 73.3% (11/15) for esophageal cancer. The results of confocal imaging coincided well with microvessel distribution on horizontal histology. Two endoscopists blindly diagnosed the two types by cellular pattern and the three types by vascular pattern: their overall accuracies were 96% and 89% for the cellular pattern and 85% and 85% for the vascular pattern, respectively. The k value of the cellular pattern and the vascular pattern diagnosis was 0.84 and 0.75, respectively. Conclusion: Scoring and quantification of confocal endomicroscopic images may be useful for the differential diagnosis and diagnosis of superficial invasion by squamous cell carcinoma.
  • Yoshiki Hirooka, Akihiro Itoh, Hiroki Kawashima, Eizaburo Ohno, Takuya Ishikawa, Hiroshi Matsubara, Yuya Itoh, Masanao Nakamura, Ryoji Miyahara, Naoki Ohmiya, Yasumasa Niwa, Masatoshi Ishigami, Yoshiaki Katano, Hidemi Goto
    Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 7(11 Suppl) S63-7-S67 2009年11月  査読有り
    Contrast-enhanced endoscopic ultrasonography (CE-EUS) and EUS-elastography are cutting-edge diagnostic modalities for pancreatic disorders. Each pancreatic disorder has characteristic hemodynamics. CE-EUS uses color Doppler flow imaging to classify pancreatic lesions into a spectrum of solid and cystic patterns. Although there is overlap in the patterns generated by specific types of tumors, some types of tumors tend to produce distinct flow images. EUS-elastography can assess tissue hardness by measuring its elasticity. This parameter appears to correlate with the malignant potential of the lesions. Tissue elasticity studies can provide information on both its pattern and distribution. The former is the conventional method of morphologic diagnosis, but it is restricted to observations made in a region of interest. The latter is an unbiased analysis that can be performed by image analysis software and is theoretically constant, regardless of regions of interest. The evolving modalities of CE-EUS and EUS-elastography might provide clinical utility in the diagnosis of pancreatic disorders.
  • Masanao Nakamura, Naoki Ohmiya, Osamu Shirai, Hiroyuki Takenaka, Morishima Kenji, Ryoji Miyahara, Takafumi Ando, Osamu Watanabe, Hiroki Kawashima, Akihiro Itoh, Yoshiki Hirooka, Yasumasa Niwa, Hidemi Goto
    HEPATO-GASTROENTEROLOGY 56(96) 1600-1605 2009年11月  査読有り
    Backgrounds/Aims: At the time of interpretation of Video Capsule Endoscopy (VCE), we sometimes see the characteristic anatomic landmarks like the major papilla of the duodenum. However, the frequency of these images and the factor affecting VCE transit are not well known. The aim of the study is to disclose the characteristics of the advance of VCE through the whole gastrointestinal tract. Methodology: We interpreted retrospectively the details of VCE with 100 patients again and analyzed the transit of VCE, significant factors affecting VCE&apos;s transit, and frequency of the anatomic landmarks observed. Results: The median esophageal transit time was 5.0 seconds; average gastric and small bowel transit times were 48.0 and 291.7 minutes. &apos;In-patient&apos; and &apos;gastric transit time&apos; were detected by statistical analysis as significant factors affecting VCE&apos;s transit to the cecum. The esophageal-cardiac junction, pyloric ring seen from the duodenal bulb, major papilla of the duodenum, ileo-cecal valve seen from the cecum, vermiform appendix, and anal canal were found with the following rates: 17, 33, 18, 20, 3, and 2 %. Conclusions: Present VCE has the limitations. This study may be the preliminary results for VCE investigating the whole gastrointestinal tract in the near future.
  • O. Watanabe, T. Ando, E. M. El-Omar, M. Shimada, K. Ina, K. Ishiguro, M. Hasegawa, N. Miyake, M. Nakamura, R. Miyahara, N. Ohmiya, Y. Niwa, H. Goto
    DIGESTIVE AND LIVER DISEASE 41(10) 735-739 2009年10月  査読有り
    Background and aims: Although cyclosporin A has been reported tube effective in the treatment of severe ulcerative colitis, factors predicting its therapeutic efficacy remain unclear. Technical progress in endoscopic ultrasonography has improved visualisation of the structure of the colon wall. Here, to assess the value of endoscopic ultrasonography in predicting the response to cyclosporin A treatment, we evaluated the therapeutic effect of cyclosporin A by determining the pre- and post-cyclosporin A thickness of the mucosal layer in the rectum using endoscopic ultrasonography with an ultrasonic catheter probe. Patients and methods: Fifteen ulcerative colitis patients who did not respond to high-closes of corticosteroids were treated with cyclosporin A by continuous intravenous infusion at 4 mg/kg/day for 20 days. Before and 20 days after cyclosporin A therapy, clinical disease activity was assessed using clinical activity index scores. Colonoscopy and endoscopic ultrasonography were undertaken before and 20 clays after cyclosporin A therapy. Results: Following treatment with cyclosporin A, nine patients showed a decrease in clinical activity index score by six points or more and were defined as responders, while the other six were defined as non-responders. Endoscopic ultrasonography measurement using an ultrasonic catheter probe showed that thickness of the rectal mucosal layer before cyclosporin A was significantly greater in responders than in non-responders (p &lt; 0.05). Further, thickness after cyclosporin A was statistically decreased (p &lt; 0.01) in the responders but not in the non-responders. Conclusions: The ultrasonic catheter probe may represent a useful means of predicting and evaluating the efficacy of cyclosporin A treatment in severely ill ulcerative colitis patients. (C) 2009 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
  • Naoki Ohmiya, Hidemi Goto, Tetsuro Nagasaka
    Gastroenterology 137(4) 1223, 538-+ 2009年10月  査読有り
  • 大宮 直木, 中村 正直, 後藤 秀実
    Gastroenterological Endoscopy 51(Suppl.2) 2063-2063 2009年9月  

書籍等出版物

 46

講演・口頭発表等

 430

共同研究・競争的資金等の研究課題

 31

メディア報道

 32