Yasunobu Fukuda
St. Marianna University School of Medicine
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Featured researches published by Yasunobu Fukuda.
Digestion | 2011
Satoshi Baba; Yoshichika Oishi; Yoshiyuki Watanabe; Ritsuko Oikawa; Ryo Morita; Yoshihito Yoshida; Tetsuya Hiraishi; Tadateru Maehata; Yoshihiko Nagase; Yasunobu Fukuda; Midori Nakazawa; Shinya Ishigouoka; Nobuhiro Hattori; Hiromu Suzuki; Minoru Toyota; Hirohumi Niwa; Michihiro Suzuki; Fumio Itoh
Background: A number of noninvasive tests have been developed to establish the presence of Helicobacter pylori infection. However, thus far these tests have only been capable of detecting its presence. An increasing number of antibiotic-resistant H. pylori infections have been reported and they are known to be correlated with 23S rRNA single nucleotide polymorphisms (SNPs). We hypothesized that genomic analysis of H. pylori recovered from gastric washes could not only be less invasive, but also useful as a screening test and for assessing the outcome of eradication therapy. Methods: Biopsy specimens and gastric washes were collected from 100 patients during endoscopic examination. Then we analyzed 23S rRNA, ureA, and cagA genes using PCR and high-throughput pyrosequencing analysis. Results: Forty-five percent (44/97) of patients tested positive for ureA and 42.3% (41/97) tested positive by a rapid urease test. One hundred percent (35/35) of patients who tested positive by both methods were observed to have the cagA gene. Among these 35 patients, 23S rRNA SNPs were present in 34.3% (12/35). Conclusions: Gastric wash-based PCR and a pyrosequencing assay were used to rapidly detect and estimate the number of 23S rRNA SNPs in clinical isolates of H. pylori. Not only is this a less invasive technique, but it can also diagnose drug resistance.
Hepatology Research | 2010
Chiaki Okuse; Hiroshi Yotsuyanagi; Norie Yamada; Masaru Okamoto; Hiroki Ikeda; Minoru Kobayashi; Yasunobu Fukuda; Hideaki Takahashi; Yoshihiko Nagase; Yuka Suzuki; Kotaro Matsunaga; Toshiya Ishii; Nobuyuki Matsumoto; Kazuhiko Koike; Michihiro Suzuki; Fumio Itoh
Aim: Nucleoside analog (NA)‐interferon (IFN) sequential therapy may enable the long‐term control of chronic hepatitis B (CHB) and the withdrawal of the nucleoside analog. We evaluated the efficacy of NA‐IFN sequential therapy for acute exacerbation of CHB.
PLOS ONE | 2016
Nobuyuki Matsumoto; Hiroki Ikeda; Ryuta Shigefuku; Nobuhiro Hattori; Tsunamasa Watanabe; Kotaro Matsunaga; Tetsuya Hiraishi; Tomohiro Tamura; Yohei Noguchi; Yasunobu Fukuda; Toshiya Ishii; Chiaki Okuse; Akira Sato; Michihiro Suzuki; Fumio Itoh
Background Decreased hemoglobin (Hb) level has been supposed to be a relatively rare side effect of a combination therapy against hepatitis C virus that consists of the NS5A inhibitor daclatasvir (DCV) and the NS3/4A protease inhibitor asunaprevir (ASV). Methods The study was conducted in 75 patients with genotype 1b chronic hepatitis C virus infection who had started combination therapy with DCV and ASV at St. Marianna University School of Medicine Hospital between September 2014 and December 2014. Results Among the patients examined, decreased Hb level by ≥1.5 g/dL from the values at treatment initiation was observed in 11 individuals. This was accompanied by decreased mean corpuscular volume, and iron and ferritin levels. Conclusions These findings suggest that the mechanism of the phenomenon is caused by iron deficiency. The underlying mechanism and clinical impacts will need to be further examined.
Hepatology Research | 2012
Chiaki Okuse; Hiroshi Yotsuyanagi; Norie Yamada; Hiroki Ikeda; Minoru Kobayashi; Yasunobu Fukuda; Hideaki Takahashi; Kotaro Matsunaga; Nobuyuki Matsumoto; Masaru Okamoto; Toshiya Ishii; Akira Sato; Kazuhiko Koike; Michihiro Suzuki; Fumio Itoh
Aim: Recently, patients positive for the low‐titer hepatitis B surface antigen (HBsAg) have been found occasionally owing to the increase in the accuracy of detection methods. The aim of this study is to clarify the clinical status of acute hepatitis B virus (HBV) infection in patients positive for low‐titer HBsAg.
The Turkish journal of gastroenterology | 2016
Hiroki Ikeda; Chiaki Okuse; Tsunamasa Watanabe; Nobuyuki Matsumoto; Kotaro Matsunaga; Ryuta Shigefuku; Nobuhiro Hattori; Tetsuya Hiraishi; Yasunobu Fukuda; Yohei Noguchi; Toshiya Ishii; Junko Shima; Kazunari Nakahara; Hiroyuki Yamamoto; Hiroshi Yasuda; Hiroshi Yotsuyanagi; Kazuhiko Koike; Fumio Itoh; Michihiro Suzuki
BACKGROUND/AIMS We compared the predictive abilities of the Abbott Real Time hepatitis C virus (HCV) assay (ART) with those of standard serum HCV ribonucleic acid (RNA) detection methods in patients undergoing triple therapy, which involves treatment with a protease inhibitor combined with pegylated interferon and ribavirin. MATERIALS AND METHODS In this study, 28 patients underwent triple therapy. The hepatitis C virus ribonucleic acid (HCV RNA) level of each patient was measured at weeks 0, 4, 8, and 12 after the initiation of therapy using the Roche COBAS AmpliPrep/COBAS TaqMan HCV assay version 1.0 (CAP/CTM v1.0) and ART. RESULTS At week 8 after the initiation of therapy, the sustained virological response (SVR) rate among patients who tested negative and positive for HCV RNA using CAP/CTM v1.0, was 80.0% (20/25) and 33.3% (1/3), and using ART, it was 91.3% (21/23) and 0.0% (0/5), respectively. Although at week 8, the predictive capability of CAP/CTM v1.0 was 78.5%, ART was found to be a more accurate predictor of future SVR status with a rate of 92.9%. CONCLUSION These results indicate that the presence or absence of serum HCV RNA, evaluated using ART at week 8 after the initiation of therapy, may be useful for predicting therapeutic outcomes in patients receiving triple therapy.
Clinical Case Reports | 2014
Goro Nagashima; Miho Kamimura; Akihito Kato; Yasunobu Fukuda; Masayuki Noda; Hiroyuki Morishima; Taku Tanaka; Yuki Umano
In‐hospital hanging during a confusional state from alcohol intoxication is rare. To treat cases of acute alcohol intoxication, careful observation will be needed to avoid accidental psychological reactions.
Human Immunology | 2004
Yasunobu Fukuda; Hiroshi Yotsuyanagi; Seido Ooka; Taichi Sekine; Junki Koike; Toshifumi Takano; Michihiro Suzuki; Fumio Itoh; Kusuki Nishioka; Tomohiro Kato
Kanzo | 2008
Naoki Izawa; Koutaro Matsunaga; Yoshihiko Nagase; Midori Nakazawa; Yasunobu Fukuda; Satoshi Baba; Nobuyuki Matsumoto; Chiaki Okuse; Yasushi Ariizumi; Yoshio Aida; Toshifumi Takano; Junki Koike; Takeshi Asakura; Takehito Otsubo; Michihiro Suzuki
Journal of Gastroenterology | 2013
Hideaki Takahashi; Michihiro Suzuki; Ryuta Shigefuku; Miki Okano; Tetsuya Hiraishi; Rei Takagi; Yohei Noguchi; Nobuhiro Hattori; Moriaki Hatsugai; Kazunari Nakahara; Masaru Okamoto; Minoru Kobayashi; Hiroki Ikeda; Yasunobu Fukuda; Yoshihiko Nagase; Toshiya Ishii; Kotaro Matsunaga; Nobuyuki Matsumoto; Chiaki Okuse; Shigeru Sase; Fumio Itoh
Kanzo | 2013
Yasunobu Fukuda; Yoshihiko Nagase; Sarika Kitagawa; Yosuke Michikawa; Tetsuya Hiraishi; Daisuke Kumon; Seiyo Ko; Satoshi Baba; Norie Yamada; Minoru Kobayashi; Hiroki Ikeda; Hideaki Takahashi; Kotaro Matsunaga; Nobuyuki Matsumoto; Chiaki Okuse; Hiroshi Yotsuyanagi; Michihiro Suzuki