Luseogliflozin improves liver fat deposition compared to metformin in type 2 diabetes patients with non‐alcoholic fatty liver disease: A prospective randomized controlled pilot study

This study aimed to assess the effect of luseogliflozin on liver fat deposition and compare luseogliflozin to metformin in type 2 diabetes (T2D) patients with non‐alcoholic fatty liver disease (NAFLD). Thirty‐two T2D patients with NAFLD diagnosed by computed tomography or abdominal sonography were r...

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Published inDiabetes, obesity & metabolism Vol. 20; no. 2; pp. 438 - 442
Main Authors Shibuya, Takashi, Fushimi, Nobutoshi, Kawai, Miyuka, Yoshida, Yohei, Hachiya, Hiroki, Ito, Shun, Kawai, Hiromi, Ohashi, Noritsugu, Mori, Akihiro
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.02.2018
Wiley Subscription Services, Inc
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Summary:This study aimed to assess the effect of luseogliflozin on liver fat deposition and compare luseogliflozin to metformin in type 2 diabetes (T2D) patients with non‐alcoholic fatty liver disease (NAFLD). Thirty‐two T2D patients with NAFLD diagnosed by computed tomography or abdominal sonography were recruited. Participants were randomly assigned to receive either luseogliflozin (2.5 mg, newly administered) or metformin (1500 mg, newly or additionally administrated). Data on the liver‐to‐spleen attenuation ratio (L/S), visceral fat area, body mass index, glycated hemoglobin (HbA1c), alanine aminotransferase (ALT), fasting plasma glucose, C‐peptide immunoreactivity (CPR), and CPR index were collected at baseline and after 6 months. The change in L/S was significantly greater in the luseogliflozin group than in the metformin group. Similarly, the changes in the visceral fat area, HbA1c, and body mass index were significantly greater in the luseogliflozin group than in the metformin group. The changes in ALT, fasting glucose, CPR, and CPR index were not significant in both groups. In conclusion, luseogliflozin significantly reduced liver fat deposition as compared to metformin, which may indicate clinical relevant benefits for NAFLD.
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ISSN:1462-8902
1463-1326
DOI:10.1111/dom.13061