Impact of a Novel Digital Therapeutics System on Nonalcoholic Steatohepatitis: The NASH App Clinical Trial

Author:

Sato Masaya12,Akamatsu Masatoshi3,Shima Toshihide4,Ikegami Tadashi5,Yanase Mikio6,Mikami Shintaro6,Imamura Jun7,Nakatsuka Takuma1,Tateishi Ryosuke1,Yamauchi Naoko8,Ushiku Tetsuo8,Okanoue Takeshi4,Fujishiro Mitsuhiro1,Hida Eisuke9,Koike Kazuhiko1

Affiliation:

1. Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan;

2. Department of Clinical Laboratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan;

3. Department of Gastroenterology, JR Tokyo General Hospital, Tokyo, Japan;

4. Department of Gastroenterology and Hepatology, Saiseikai Suita Hospital, Osaka, Japan;

5. Division of Gastroenterology and Hepatology, Tokyo Medical University Ibaraki Medical Center, Ibaraki, Japan;

6. Department of Gastroenterology and Hepatology, National Center for Global Health and Medicine, Tokyo, Japan;

7. Department of Hepatology, Tokyo Metropolitan Cancer an Infectious Disease Center Komagome Hospital, Tokyo, Japan;

8. Department of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan;

9. Department of Biostatics and Data Science, Osaka University Graduate School of Medicine, Osaka, Japan.

Abstract

INTRODUCTION: Management of nonalcoholic steatohepatitis (NASH) is a currently unmet clinical need. Digital therapeutics (DTx) is an emerging class of medicine that delivers evidence-based therapeutic interventions. This study was aimed at investigating the efficacy of DTx in patients with NASH. METHODS: We conducted a multicenter, single-arm, 48-week trial in 19 patients with biopsy-confirmed NASH. All patients received a DTx intervention with a newly developed smartphone application. The primary endpoint was change in the nonalcoholic fatty liver disease activity score (NAS) without worsening of liver fibrosis. The secondary endpoints included improvement of the NAS by ≥2 points without worsening of liver fibrosis, change in the body weight, and regression of fibrosis. RESULTS: After the 48-week DTx intervention, improvement of the NAS was observed in 68.4% (13/19) of patients. The mean change in the NAS from baseline to the end of the intervention was −2.05 ± 1.96 (P < 0.001 when compared with the threshold of −0.7). A decrease in the NAS by ≥ 2 points was achieved in 11 (57.9%). The average weight loss at the end of the intervention was 8.3% (P < 0.001). Reduction of the fibrosis stage was observed in 58.3% when the analysis was limited to patients with stage F2/3 fibrosis. There were no serious adverse events that could be considered as being related to the DTx intervention. DISCUSSION: DTx for NASH was found to be highly efficacious and well-tolerated. Further evaluation of the DTx intervention for NASH in a phase 3 trial is warranted.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Hepatology

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