PMID- 32448832 OWN - NLM STAT- MEDLINE DCOM- 20201223 LR - 20201223 IS - 1349-7235 (Electronic) IS - 0918-2918 (Print) IS - 0918-2918 (Linking) VI - 59 IP - 16 DP - 2020 Aug 15 TI - SGLT2 Inhibitor Treatment Outcome in Nonalcoholic Fatty Liver Disease Complicated with Diabetes Mellitus: The Long-term Effects on Clinical Features and Liver Histopathology. PG - 1931-1937 LID - 10.2169/internalmedicine.4398-19 [doi] AB - Objective The aim of this study was to determine the long-term effects of a sodium-glucose cotransporter 2 inhibitor (SGLT2i) in nonalcoholic fatty liver disease (NAFLD) patients with type 2 diabetes mellitus (T2DM) on the clinical features and liver histopathology. Methods In this retrospective study, the long-term histological impacts of SGLT2i in NAFLD patients with T2DM were investigated. Patients Seven patients with NAFLD and T2DM were treated for the long term with 100 mg/day canagliflozin, an SGLT2i, and liver biopsies were obtained at the 3 points of pretreatment, 24 weeks, and >/=1 year (third liver biopsy) after the start of treatment. Six of seven patients were evaluated with third liver biopsy at the point of three or more years. The primary outcome was liver histopathological changes (defined as a decrease in the NAFLD activity score of one point or more without worsening of the fibrosis stage, compared to pretreatment). Results All 7 patients showed worsening of body mass index and waist circumference at the third liver biopsy compared to 24 weeks. However, the scores of steatosis, lobular inflammation, ballooning, and fibrosis stage improved at the third liver biopsy in 57%, 43%, 14%, and 29% of the patients, respectively, compared to pretreatment. One of the seven patients showed histopathological worsening at the third liver biopsy compared to pretreatment, but the improvement was maintained in the other six patients. Conclusion The long-term treatment of NAFLD complicated by T2DM using an SGLT2i is associated with long-term improvement in liver histopathology despite the worsening of clinical features. FAU - Akuta, Norio AU - Akuta N AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. FAU - Kawamura, Yusuke AU - Kawamura Y AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. FAU - Fujiyama, Shunichiro AU - Fujiyama S AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. FAU - Sezaki, Hitomi AU - Sezaki H AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. FAU - Hosaka, Tetsuya AU - Hosaka T AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. FAU - Kobayashi, Masahiro AU - Kobayashi M AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. FAU - Kobayashi, Mariko AU - Kobayashi M AD - Liver Research Laboratory, Toranomon Hospital, Japan. FAU - Saitoh, Satoshi AU - Saitoh S AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. FAU - Suzuki, Fumitaka AU - Suzuki F AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. FAU - Suzuki, Yoshiyuki AU - Suzuki Y AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. FAU - Arase, Yasuji AU - Arase Y AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. FAU - Ikeda, Kenji AU - Ikeda K AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. FAU - Kumada, Hiromitsu AU - Kumada H AD - Department of Hepatology, Toranomon Hospital and Okinaka Memorial Institute for Medical Research, Japan. LA - eng PT - Journal Article DEP - 20200523 PL - Japan TA - Intern Med JT - Internal medicine (Tokyo, Japan) JID - 9204241 RN - 0 (Sodium-Glucose Transporter 2 Inhibitors) SB - IM MH - Adult MH - Biopsy MH - Body Weights and Measures MH - Diabetes Mellitus, Type 2/*drug therapy/*epidemiology MH - Female MH - Humans MH - Japan/epidemiology MH - Male MH - Middle Aged MH - Non-alcoholic Fatty Liver Disease/*epidemiology/*pathology MH - Retrospective Studies MH - Sodium-Glucose Transporter 2 Inhibitors/*therapeutic use MH - Treatment Outcome PMC - PMC7492114 OTO - NOTNLM OT - SGLT2 inhibitor OT - diabetes mellitus OT - fibrosis stage OT - hepatocyte steatosis OT - liver biopsy OT - long-term OT - nonalcoholic fatty liver disease OT - nonalcoholic steatohepatitis COIS- Author's disclosure of potential Conflicts of Interest (COI). Norio Akuta: Honoraria, Mitsubishi Tanabe Pharma, AbbVie and Gilead Sciences. Masahiro Kobayashi: Honoraria, Eisai. Yasuji Arase: Honoraria, AbbVie. Hiromitsu Kumada: Honoraria, MSD, Gilead Sciences, AbbVie, Eisai and Dainippon Sumitomo Pharma. EDAT- 2020/05/26 06:00 MHDA- 2020/12/29 06:00 PMCR- 2020/08/15 CRDT- 2020/05/26 06:00 PHST- 2020/05/26 06:00 [pubmed] PHST- 2020/12/29 06:00 [medline] PHST- 2020/05/26 06:00 [entrez] PHST- 2020/08/15 00:00 [pmc-release] AID - 10.2169/internalmedicine.4398-19 [doi] PST - ppublish SO - Intern Med. 2020 Aug 15;59(16):1931-1937. doi: 10.2169/internalmedicine.4398-19. Epub 2020 May 23.