Sho, Takuya
Suda, Goki https://orcid.org/0000-0003-0098-9106
Ohara, Masatsugu
Kohya, Risako
Sasaki, Takashi
Yoshida, Sonoe
Hosoda, Shunichi
Ogawa, Koji
Kitagataya, Takashi
Maehara, Osamu
Ohnishi, Shunsuke
Kawagishi, Naoki
Natsuizaka, Mitsuteru
Nakai, Masato
Baba, Masaru
Yamamoto, Yoshiya
Tsukuda, Yoko
Meguro, Takashi
Yamada, Ren
Kobayashi, Tomoe
Takagi, Tomofumi
Sakamoto, Naoya
,
Funding for this research was provided by:
AMED (JP24fk0210126, JP24fk0310501, JP24fk0210121, JP24fk0210112, JP24fk0210142, JP24fk0210111, JP24fk0310524, JP24fk0210123, JP24fk0210157, JP24fk0310518, JP24fk0210103, JP24fk0210104, JP24fk0210113, JP24fk0210143)
Article History
Accepted: 14 August 2024
First Online: 2 September 2024
Declarations
:
: This study was partly supported by grants from the Japan Agency for Medical Research and Development (AMED; grant nos. JP24fk0210126, JP24fk0310501, JP24fk0210121, JP24fk0210112, JP24fk0210142, JP24fk0210111, JP24fk0310524, JP24fk0210123, JP24fk0210157, JP24fk0310518, JP24fk0210103, JP24fk0210104, JP24fk0210113, and JP24fk0210143).
: Professor Naoya Sakamoto received lecture fees from Chugai Pharmaceutical Co., Ltd. and research grants from Gilead Sciences, Inc. and AbbVie, Inc. Dr. Goki Suda received research grants from Gilead Sciences. Takuya Sho, Masatsugu Ohara, Risako Kohya, Takashi Sasaki, Sonoe Yoshida, Shunichi Hosoda, Koji Ogawa, Takashi Kitagataya, Osamu Maehara, Shunsuke Ohnishi, Naoki Kawagishi, Mitsuteru Natsuizaka, Masato Nakai, Masaru Baba, Yoshiya Yamamoto, Yoko Tsukuda, Takashi Meguro, Ren Yamada, Tomoe Kobayashi, and Tomofumi Takagi declare that they have no conflicts of interest that might be relevant to the contents of this manuscript.
: The ethics committee of Hokkaido University Hospital verified that the study protocol (institutional review board no.: 023-0141) adhered to the ethical guidelines of the Declaration of Helsinki.
: Patients who provided written informed consent or did not express their refusal to participate were included in this study. Additionally, the ethics committee of Hokkaido University Hospital granted specific approval for the inclusion of patients who did not actively refuse to participate as an alternative to obtaining written informed consent.
: Not applicable.
: This article includes all data generated or analyzed during this study, as well as the supplementary data. Further inquiries can be directed to the corresponding author.
: G.S. designed the study. T.Sho, G.S., and M.O. performed examinations and statistical analyses. T.S. and G.S. revised the manuscript. T.Sho, R.K., G.S., M.O., S.H., T.Sasaki, S.Y., K.O., T.K., O.M., Y.T., S.O., N.K., M.Natsuizaka, M.Nakai, M.B., Y.Y., T.M., R.Y., T.T., and T.K. collected samples and clinical data. M.Natsuizaka, K.O., and N.S. provided hepatological advice. N.S. revised the manuscript for the intellectual content.