TY - JOUR
T1 - Accuracy of non-invasive scoring systems for diagnosing non-alcoholic steatohepatitis-related fibrosis
T2 - Multicenter validation study
AU - Itoh, Yoshito
AU - Seko, Yuya
AU - Shima, Toshihide
AU - Nakajima, Tomoaki
AU - Mizuno, Kei
AU - Kawamura, Yusuke
AU - Akuta, Norio
AU - Ito, Kiyoaki
AU - Kawanaka, Miwa
AU - Hiramatsu, Akira
AU - Sakamoto, Michiie
AU - Harada, Kenichi
AU - Goto, Yoshihito
AU - Nakayama, Takeo
AU - Kumada, Hiromitsu
AU - Okanoue, Takeshi
N1 - Funding Information:
Correspondence: Dr Takeshi Okanoue, Department of Gastroenterology, Saiseikai Suita Hospital, 1-2 Kawazonocho, Suita, 564-0013, Japan. Email: okanoue@suita.saiseikai.or.jp Conflict of interest: Yoshito Itoh received a research grant from Sumitomo Dainippon Pharma. Kiyoaki Ito received a research grant from Gilead Sciences. Hiromitsu Kumada received lecture fees from Merck Sharp and Dohme, Bristol-Myers Squibb Company, AbbVie, Gilead Sciences, and Sumitomo Dainippon Pharma. Financial support: This research was supported in part by the Research Program on Hepatitis from the Japan Agency for Medical Research and Development (T.O.). The study was funded by Sumitomo Dainippon Pharma. †These authors contributed equally to this work Received 30 May 2018; revision 28 June 2018; accepted 29 June 2018.
Funding Information:
THE AUTHORS ARE grateful to Dr. Motoh Iwasa (Department of Gastroenterology and Hepatology, Graduate School of Medicine, Mie University), Dr. Keisuke Hino (Department of Hepatology and Pancreatology, Kawasaki Medical School), Dr. Yuichiroh Eguchi (Liver Center, Saga University), Dr. Kazuo Notsumata (Fukuiken Saiseikai Hospital), Dr. Akio Ido (Department of Digestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences), Dr. Masataka Seike (Department of Gastroenterology, Faculty of Medicine, Oita University), Dr. Toshiji Saibara (Department of Gastroenterology and Hepatology, Kochi Medical School), Dr. Shuichi Kaneko (Department of Gastroenterology, Kanazawa University Graduate School of Medical Science), and Dr. Kazuhiro Hamaoka (Eguchi Hospital) for recruiting subjects. This research was supported in part by the Research Program on Hepatitis from the Japan Agency for Medical Research and Development, AMED (T.O.). The study was funded by Sumitomo Dainippon Pharma. The funder partly contributed to the design of the study protocol, but did not play any additional role in data collection, analysis, or preparation of the manuscript.
Funding Information:
The authors are grateful to Dr. Motoh Iwasa (Department of Gastroenterology and Hepatology, Graduate School of Medicine, Mie University), Dr. Keisuke Hino (Department of Hepatology and Pancreatology, Kawasaki Medical School), Dr. Yuichiroh Eguchi (Liver Center, Saga University), Dr. Kazuo Notsumata (Fukuiken Saiseikai Hospital), Dr. Akio Ido (Department of Digestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences), Dr. Masataka Seike (Department of Gastroenterology, Faculty of Medicine, Oita University), Dr. Toshiji Saibara (Department of Gastroenterology and Hepatology, Kochi Medical School), Dr. Shuichi Kaneko (Department of Gastroenterology, Kanazawa University Graduate School of Medical Science), and Dr. Kazuhiro Hamaoka (Eguchi Hospital) for recruiting subjects. This research was supported in part by the Research Program on Hepatitis from the Japan Agency for Medical Research and Development, AMED (T.O.). The study was funded by Sumitomo Dainippon Pharma. The funder partly contributed to the design of the study protocol, but did not play any additional role in data collection, analysis, or preparation of the manuscript.
Publisher Copyright:
© 2018 The Japan Society of Hepatology
PY - 2018/12
Y1 - 2018/12
N2 - Aim: Hepatic fibrosis is the most important factor for estimating the prognosis of patients with non-alcoholic fatty liver disease (NAFLD). A novel non-invasive scoring system, the FM-fibro index, showed high accuracy in a pilot study. The purpose of this study was to validate the efficacy of the FM-fibro index in a multicenter cohort. Methods: Among 18 institutions, we analyzed 400 Japanese patients with biopsy-proven NAFLD. We evaluated the accuracies of the FM-fibro index, CA-fibro index, and European Liver Fibrosis (ELF) panel by area under the receiver operator characteristics curves (AUROC). The FM-fibro index includes three formulas for type IV collagen 7S, hyaluronic acid, and vascular cell adhesion molecule-1. Results: Among 400 patients, 205 were women, and the median age was 56 years. The histological distribution of Matteoni types 1, 2, 3, and 4 was 11, 40, 15, and 334, and the distribution of hepatic fibrosis stages 0 to 4 was 67, 183, 55, 63, and 32, respectively. The AUROCs of the FM-fibro index, CA-fibro index, and ELF panel for non-alcoholic steatohepatitis (NASH)-related fibrosis were 0.7178/0.7095/0.7065, 0.7093, and 0.7245, respectively. The sensitivity and specificity of the FM-fibro index for predicting NASH-related fibrosis was 0.5359/0.5210/0.4641 and 0.8333/0.8182/0.8788, respectively. The accuracy of the FM-fibro index was not significantly different from that of the CA-fibro index or the ELF panel. Conclusions: The FM-fibro index can predict NASH-related fibrosis with sufficient accuracy compared with previous scoring systems. Further analyses that verify the accuracy of the FM-fibro index to distinguish significant or advanced fibrosis in patients with NAFLD are awaited. (UMIN-CTR: UMIN000018158).
AB - Aim: Hepatic fibrosis is the most important factor for estimating the prognosis of patients with non-alcoholic fatty liver disease (NAFLD). A novel non-invasive scoring system, the FM-fibro index, showed high accuracy in a pilot study. The purpose of this study was to validate the efficacy of the FM-fibro index in a multicenter cohort. Methods: Among 18 institutions, we analyzed 400 Japanese patients with biopsy-proven NAFLD. We evaluated the accuracies of the FM-fibro index, CA-fibro index, and European Liver Fibrosis (ELF) panel by area under the receiver operator characteristics curves (AUROC). The FM-fibro index includes three formulas for type IV collagen 7S, hyaluronic acid, and vascular cell adhesion molecule-1. Results: Among 400 patients, 205 were women, and the median age was 56 years. The histological distribution of Matteoni types 1, 2, 3, and 4 was 11, 40, 15, and 334, and the distribution of hepatic fibrosis stages 0 to 4 was 67, 183, 55, 63, and 32, respectively. The AUROCs of the FM-fibro index, CA-fibro index, and ELF panel for non-alcoholic steatohepatitis (NASH)-related fibrosis were 0.7178/0.7095/0.7065, 0.7093, and 0.7245, respectively. The sensitivity and specificity of the FM-fibro index for predicting NASH-related fibrosis was 0.5359/0.5210/0.4641 and 0.8333/0.8182/0.8788, respectively. The accuracy of the FM-fibro index was not significantly different from that of the CA-fibro index or the ELF panel. Conclusions: The FM-fibro index can predict NASH-related fibrosis with sufficient accuracy compared with previous scoring systems. Further analyses that verify the accuracy of the FM-fibro index to distinguish significant or advanced fibrosis in patients with NAFLD are awaited. (UMIN-CTR: UMIN000018158).
KW - FM-fibro index
KW - liver fibrosis
KW - non-alcoholic fatty liver disease
UR - http://www.scopus.com/inward/record.url?scp=85052719483&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85052719483&partnerID=8YFLogxK
U2 - 10.1111/hepr.13226
DO - 10.1111/hepr.13226
M3 - Article
AN - SCOPUS:85052719483
SN - 1386-6346
VL - 48
SP - 1099
EP - 1107
JO - Hepatology Research
JF - Hepatology Research
IS - 13
ER -