Yoshiyasu Kono

Dr. Yoshiyasu Kono

Gastroenterology and Hepatology, Okayama University, Okayama, Japan
orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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11 July 2017 in Journal of Gastroenterology and Hepatology
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Journal Article
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YKYoshiyasu Kono
Yoshiyasu Kono
YOYuka Obayashi
Yuka Obayashi
YBYuki Baba
Yuki Baba
HSHiroyuki Sakae
Hiroyuki Sakae
TGTatsuhiro Gotoda
Tatsuhiro Gotoda
HOHiroyuki Okada
Hiroyuki Okada

29 October 2018 in Journal of Gastroenterology
Verified
Journal Article
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YKYoshiyasu Kono
Yoshiyasu Kono
HKHiromitsu Kanzaki
Hiromitsu Kanzaki
TTTakao Tsuzuki
Takao Tsuzuki
MTMasahiro Takatani
Masahiro Takatani
JNJunichirou Nasu
Junichirou Nasu
HOHiroyuki Okada
Hiroyuki Okada

21 January 2021 in Targeted Oncology
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Journal Article
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YKYoshiyasu Kono
Yoshiyasu Kono
YCYasuhiro Choda
Yasuhiro Choda
MNMasahiro Nakagawa
Masahiro Nakagawa
KMKoji Miyahara
Koji Miyahara
MIMichihiro Ishida
Michihiro Ishida
HOHiroyuki Okada
Hiroyuki Okada

3 January 2017 in Digestive Diseases and Sciences
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Journal Article
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YKYoshiyasu Kono
Yoshiyasu Kono
MMMinoru Matsubara
Minoru Matsubara
TTTatsuya Toyokawa
Tatsuya Toyokawa
RTRyuta Takenaka
Ryuta Takenaka
SSSeiyu Suzuki
Seiyu Suzuki
HOHiroyuki Okada
Hiroyuki Okada

Verified
Journal Article
Open access
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DKDaisuke Kametaka
Daisuke Kametaka
MIMasaya Iwamuro
Masaya Iwamuro
TTTakahide Takahashi
Takahide Takahashi
AHAraki Hirabata
Araki Hirabata
KHKenta Hamada
Kenta Hamada
HOHiroyuki Okada
Hiroyuki Okada
Data regarding the in-depth surface marker profiles of gastric tissue-resident lymphocytes in autoimmune and Helicobacter pylori-associated gastritis are lacking. In this study, we investigated potential differences in lymphocyte composition between these profiles. We enrolled patients with autoimmune (n = 14), active (current infection of H. pylori in the stomach; n = 10), and inactive gastritis (post-eradication of H. pylori; n = 20). Lymphocytes were isolated from the greater curvature of the stomach and lesser curvature of the body and analyzed using flow cytometry. The CD8+/CD3+ and CD4+/CD3+ ratios differed between the samples. Body CD4+/antrum CD4+, which is calculated by dividing the CD4+/CD3+ ratio in the body by that in the antrum, was significantly higher in autoimmune gastritis (3.54 ± 3.13) than in active (1.47 ± 0.41) and inactive gastritis (1.42 ± 0.77). Antrum CD8+/CD4+ in autoimmune gastritis (7.86 ± 7.23) was also higher than that in active (1.49 ± 0.58) and inactive gastritis (2.84 ± 2.17). The area under the receiver operating characteristic curve of antrum CD8+/CD4+ was 0.842, and the corresponding optimal cutoff point was 4.0, with a sensitivity of 71.4% and a specificity of 93.3%. We propose that an antrum CD8+/CD4+ ratio > 4.0 is a potential diagnostic marker for autoimmune gastritis.

1 December 2020
Verified
Journal Article
Closed access
YKYoshiyasu Kono
Yoshiyasu Kono
HKHiromitsu Kanzaki
Hiromitsu Kanzaki
MIMasaya Iwamuro
Masaya Iwamuro
SKSeiji Kawano
Seiji Kawano
YKYoshiro Kawahara
Yoshiro Kawahara
HOHiroyuki Okada
Hiroyuki Okada