PMID- 30603325 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20201001 IS - 2190-1678 (Print) IS - 2190-1686 (Electronic) IS - 2190-1678 (Linking) VI - 8 IP - 2 DP - 2017 Jun TI - The effects of ipragliflozin on the liver-to-spleen attenuation ratio as assessed by computed tomography and on alanine transaminase levels in Japanese patients with type 2 diabetes mellitus. PG - 218-227 LID - 10.1007/s13340-016-0302-y [doi] AB - We assessed the effects of a 12-week ipragliflozin treatment on the liver-to-spleen attenuation ratio (L/S ratio) using computed tomography and on alanine transaminase (ALT) levels in Japanese patients with type 2 diabetes mellitus (T2DM). Sixty-two patients with T2DM [age, 56 +/- 8 years; hemoglobin A1c (HbA1c) levels, 8.1 +/- 0.9%; body mass index (BMI), 27.5 +/- 3.3 kg/m(2)] were randomly assigned in a 2:1 ratio to receive ipragliflozin (50 mg/day; ipragliflozin group; n = 40) or continued treatment (control group; n = 22) for 12 weeks. The primary endpoints were changes in ALT levels; the secondary endpoints included changes in the L/S ratio and in the visceral fat area (VFA) and subcutaneous fat area (SFA) before and after 12 weeks of the treatment as assessed by computed tomography. ALT levels (-12.45 vs. +5.82 IU/l, P < 0.001), L/S ratio (+0.07 vs. -0.08, P < 0.001), SFA (-5.8 vs. +13.3 cm(2), P < 0.05), and VFA (+1.4 vs. +20.4 cm(2), P < 0.05) significantly changed from baseline in the ipragliflozin group compared with the values in the control group. Multiple regression analysis among all subjects revealed that the independent factor contributing to the %DeltaALT and %DeltaL/C ratio was treatment group alone (ipragliflozin group = 1; control group = 0; beta coefficient = -32.08, P < 0.001 and beta coefficient = 19.98, P < 0.05, respectively). Thus, ipragliflozin may lower ALT levels associated with increased L/S ratios, indicating its potential therapeutic efficacy in T2DM-associated hepatic steatosis. FAU - Bando, Yukihiro AU - Bando Y AD - Department of Internal Medicine, Fukui-ken Saiseikai Hospital, Funabashi 7-1, Wadanaka-Machi, Fukui, 918-8503 Japan. ISNI: 0000 0004 1774 4989. GRID: grid.415130.2 FAU - Ogawa, Ayumi AU - Ogawa A AD - Department of Internal Medicine, Fukui-ken Saiseikai Hospital, Funabashi 7-1, Wadanaka-Machi, Fukui, 918-8503 Japan. ISNI: 0000 0004 1774 4989. GRID: grid.415130.2 FAU - Ishikura, Kazuhide AU - Ishikura K AD - Department of Internal Medicine, Fukui-ken Saiseikai Hospital, Funabashi 7-1, Wadanaka-Machi, Fukui, 918-8503 Japan. ISNI: 0000 0004 1774 4989. GRID: grid.415130.2 FAU - Kanehara, Hideo AU - Kanehara H AD - Department of Internal Medicine, Fukui-ken Saiseikai Hospital, Funabashi 7-1, Wadanaka-Machi, Fukui, 918-8503 Japan. ISNI: 0000 0004 1774 4989. GRID: grid.415130.2 FAU - Hisada, Azusa AU - Hisada A AD - Department of Internal Medicine, Fukui-ken Saiseikai Hospital, Funabashi 7-1, Wadanaka-Machi, Fukui, 918-8503 Japan. ISNI: 0000 0004 1774 4989. GRID: grid.415130.2 FAU - Notumata, Kazuo AU - Notumata K AD - Department of Internal Medicine, Fukui-ken Saiseikai Hospital, Funabashi 7-1, Wadanaka-Machi, Fukui, 918-8503 Japan. ISNI: 0000 0004 1774 4989. GRID: grid.415130.2 FAU - Okafuji, Kazuhiro AU - Okafuji K AD - Department of Internal Medicine, Fukui-ken Saiseikai Hospital, Funabashi 7-1, Wadanaka-Machi, Fukui, 918-8503 Japan. ISNI: 0000 0004 1774 4989. GRID: grid.415130.2 FAU - Toya, Daisyu AU - Toya D AD - Department of Internal Medicine, Fukui-ken Saiseikai Hospital, Funabashi 7-1, Wadanaka-Machi, Fukui, 918-8503 Japan. ISNI: 0000 0004 1774 4989. GRID: grid.415130.2 LA - eng PT - Journal Article DEP - 20170103 PL - Japan TA - Diabetol Int JT - Diabetology international JID - 101553224 PMC - PMC6224952 OTO - NOTNLM OT - Alanine transaminase OT - Ipragliflozin OT - L/S ratio on computed tomography OT - Type 2 diabetes mellitus COIS- Yukihiro Bando has served on advisory boards for Astellas Pharma, Inc. Yukihiro Bando has received speaker honoraria from Astellas Pharma, Inc., Eli Lilly Japan K.K., Sanofi K.K., Novo Nordisk Pharma, Ltd., Novartis Pharma K.K., MSD K.K., and Takeda Pharmaceutical Co., Ltd. None of the other authors declare a conflict of interest.All procedures conducted in this study were in accordance with the ethics committee of Fukui-ken Saiseikai Hospital and with the Helsinki Declaration of 1964 and later revision. Informed consent or substitute for it was obtained from all patients for being included in the study. Identifying information of patients of human subjects, including names, initials, addresses, admission dates, hospital numbers, or any other data that might identify patients were not included in our written descriptions. EDAT- 2017/01/03 00:00 MHDA- 2017/01/03 00:01 PMCR- 2018/01/03 CRDT- 2019/01/04 06:00 PHST- 2016/08/29 00:00 [received] PHST- 2016/12/20 00:00 [accepted] PHST- 2019/01/04 06:00 [entrez] PHST- 2017/01/03 00:00 [pubmed] PHST- 2017/01/03 00:01 [medline] PHST- 2018/01/03 00:00 [pmc-release] AID - 302 [pii] AID - 10.1007/s13340-016-0302-y [doi] PST - epublish SO - Diabetol Int. 2017 Jan 3;8(2):218-227. doi: 10.1007/s13340-016-0302-y. eCollection 2017 Jun.