J-GLOBAL ID:201801008681123309   Update date: May. 01, 2024

KATO Koichi

カトウ コウイチ | KATO Koichi
Affiliation and department:
Research field  (1): Cardiology
Research keywords  (4): Brugada syndrome ,  Long QT syndrome ,  Laminopathy ,  遺伝性不整脈
Research theme for competitive and other funds  (8):
  • 2023 - 2026 QT延長とブルガダ症候群の合併を来すCa2+チャネル変異の機序解明を目指す研究
  • 2022 - 2025 バイオインフォマティクスを用いた非コードDNA解析による若年突然死の発症機序解明
  • 2023 - 2024 山内進循環器病研究助成
  • 2021 - 2024 The elucidation of complicated genetic backgrounds and pathogenicity in patients with inherited primary arrhythmia syndromes caused by unknown etiology
  • 2023 - 2024 持田記念医学薬学振興財団研究助成
Show all
Papers (53):
  • Asami Kashiwa, Hideki Itoh, Takeru Makiyama, Yuko Wada, Junichi Ozawa, Koichi Kato, Megumi Fukuyama, Tadashi Nakajima, Seiko Ohno, Minoru Horie. Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants. Heart Rhythm. 2024
  • Masao Yoshinaga, Yumiko Ninomiya, Yuji Tanaka, Megumi Fukuyama, Koichi Kato, Seiko Ohno, Minoru Horie, Hiromitsu Ogata. Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome. Circulation journal : official journal of the Japanese Circulation Society. 2023
  • Yusuke Okuyama, Tomoya Ozawa, Takuma Nishikawa, Yusuke Fujii, Koichi Kato, Yoshihisa Sugimoto, Yoshihisa Nakagawa, Takashi Ashihara. Association with the nonparoxysmal atrial fibrillation duration and outcome of ExTRa Mapping-guided rotor ablation. Journal of arrhythmia. 2023. 39. 4. 531-538
  • Megumi Fukuyama, Minoru Horie, Koichi Kato, Hisaaki Aoki, Shuhei Fujita, Yoko Yoshida, Hisanori Sakazaki, Takako Toda, Michihiko Ueno, Gaku Izumi, et al. Calmodulinopathy in Japanese Children - Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy. Circulation journal : official journal of the Japanese Circulation Society. 2023
  • Jingshan Gao, Takeru Makiyama, Yuta Yamamoto, Takuya Kobayashi, Hisaaki Aoki, Thomas L Maurissen, Yimin Wuriyanghai, Asami Kashiwa, Tomohiko Imamura, Takanori Aizawa, et al. Novel Calmodulin Variant p.E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. Circulation. Arrhythmia and electrophysiology. 2023. 16. 3. e011387
MISC (18):
  • GAO Jingshan, MAKIYAMA Takeru, YAMAMOTO Yuta, KOBAYASHI Takuya, AOKI Hisaaki, MAURISSEN L Thomas, KASHIWA Asami, IMAMURA Tomohiko, AIZAWA Takanori, HUANG Hai, et al. Novel CPVT-Associated Calmodulin Mutation Activating RyR2 Channels Causes Robust Arrhythmogenicity in iPS Cell Model. 日本不整脈心電学会学術大会プログラム・抄録集(Web). 2022. 68th
  • IMAMURA Tomohiko, MAKIYAMA Takeru, OZAWA Junichi, HUANG Hai, AIZAWA Takanori, GAO Jingshan, KASHIWA Asami, KOHJITANI Hirohiko, KATO Koichi, AOKI Hisaaki, et al. Clinical Characteristics and Risk Stratification in Pediatric Brugada Syndrome. 日本不整脈心電学会学術大会プログラム・抄録集(Web). 2022. 68th
  • 今村知彦, 牧山武, 小澤淳一, 相澤卓範, 柏麻美, 糀谷泰彦, 加藤浩一, 青木寿明, 鈴木博, 園田桂子, et al. Clinical Aspects of Brugada Syndrome in Children: The Impact of Gender and Age on the Prognosis. 日本循環器学会学術集会(Web). 2022. 86th
  • 今村知彦, 牧山武, 小澤淳一, 相澤卓範, 柏麻美, 山本雄大, 糀谷泰彦, 加藤浩一, 青木寿明, 大野聖子, et al. Clinical Characteristics of Pediatric Brugada Syndrome in Japanese Registry. 日本循環器学会学術集会(Web). 2021. 85th
  • 加藤 浩一, 大野 聖子, 中川 義久, 堀江 稔. 遺伝性循環器疾患に対する遺伝子解析の実践 致死性遺伝性不整脈に対する遺伝子診断 当院における現状と課題. 日本心臓病学会学術集会抄録. 2019. 67回. S7-2
Lectures and oral presentations  (20):
  • The dominant-negative effect of Nav 1.5 variants through channel dimerization does not play a crucial role in determining a phenotype severity
  • The dominant-negative effect of Loss of function Nav 1.5 variants is not a critical determinant of phenotype severity
    (ESC Congress 2023 2023)
  • Compound heterozygous SCN5A variants caused severe bradyarrhythmia via complex channel-channel interaction.
    (Japanese Circulation Society Annual Meeting 2023)
  • Correction of cryptic donor site splicing by antisense oligo nucleotides in a case of Brugada syndrome.
    (Japanese Circulation Society Annual Meeting 2023)
  • Correction of SCN5A splicing error of Brugada syndrome patient by antisense oligo nucleotides
    (Asia Pacific Heart Rhythm Society 2022 2022)
Education (2):
  • 2010 - 2014 Shiga University of Medical Science Graduate School of Medicine
  • 1999 - 2005 Shiga University of Medical Science Undergraduate School of Medicine Faculty of Medicine
Professional career (1):
  • Ph. D (Shiga University of Medical Science)
Work history (8):
  • 2018/04 - 現在 Shiga University of Medical Science
  • 2016/03 - 2018/03 INSERM, Université Pierre et Marie Curie UMRS1166 Ingénieur de recherche
  • 2015/10 - 2016/02 Shiga University of Medical Science
  • 2014/06 - 2015/09 Shiga University of Medical Science
  • 2014/04 - 2014/05 滋賀医科大学附属病院 循環器内科 医員
Show all
Committee career (2):
  • 2021/12 - 現在 日本不整脈心電学会 不整脈専門医試験問題作成委員
  • 2020 - 現在 日本循環器学会近畿支部 評議員
Awards (3):
  • 2023/05 - 公益財団法人循環器病研究振興財団 山内進循環器病研究助成
  • 2016 - l’Institut de France Le Foulon Delalande bourse de recherche Etude de variants de la protéine SAP97 dans le syndrome de Brugada.
  • 2015 - 日本心電学会 海外留学助成
Association Membership(s) (4):
※ Researcher’s information displayed in J-GLOBAL is based on the information registered in researchmap. For details, see here.

Return to Previous Page