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Metabolic changes induced by dapagliflozin, an SGLT2 inhibitor, in Japanese patients with type 2 diabetes treated by oral anti-diabetic agents: A randomized, clinical trial.
Horibe, Kayo; Morino, Katsutaro; Miyazawa, Itsuko; Tanaka-Mizuno, Sachiko; Kondo, Keiko; Sato, Daisuke; Ohashi, Natsuko; Ida, Shogo; Yanagimachi, Tsuyoshi; Yoshimura, Masahiro; Itoh, Ryuta; Murata, Kiyoshi; Miura, Katsuyuki; Arima, Hisatomi; Fujita, Yukihiro; Ugi, Satoshi; Maegawa, Hiroshi.
Afiliação
  • Horibe K; Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Morino K; Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan; Institutional Research Office, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan. Electronic address: morino@belle.shiga-med.ac.jp.
  • Miyazawa I; Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan; Education Center for Medicine and Nursing, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Tanaka-Mizuno S; Department of Medical Statistics, Shiga University of Medical Science, Shiga 520-2192, Japan; Department of Pharmacoepidemiology, Kyoto University Graduate School of Medicine and Public Health, Kyoto 606-8501, Japan.
  • Kondo K; Department of Public Health, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Sato D; Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Ohashi N; Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan; Department of Stem Cell Biology and Regenerative Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Ida S; Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Yanagimachi T; Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Yoshimura M; Department of Radiology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Itoh R; Department of Radiology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Murata K; Department of Radiology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan; Rakusai New Town Hospital, Kyoto 610-1142, Japan.
  • Miura K; Department of Public Health, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Arima H; Department of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka 814-0133, Japan.
  • Fujita Y; Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Ugi S; Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
  • Maegawa H; Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Diabetes Res Clin Pract ; 186: 109781, 2022 Apr.
Article em En | MEDLINE | ID: mdl-35181350
ABSTRACT

AIM:

We aimed to determine whether SGLT2 inhibitor dapagliflozin treatment affects body composition and amino acid (AA) metabolism.

METHODS:

Fifty-two overweight patients treated by oral antidiabetic agents were randomly assigned to dapagliflozin (Dapa) or a standard treatment (Con) and followed for 24 weeks. The primary outcome was the change in body mass (BM) between baseline and week 24. Body composition, intrahepatic triglyceride (IHTG) content, and plasma AA concentrations were examined as secondary outcomes.

RESULTS:

The change in BM was significantly larger in the Dapa than in the Con group, with a difference in the mean change of -1.72 kg (95 %CI -2.85, -0.59; P = 0.004) between the groups. Total fat mass was reduced by dapagliflozin treatment, but fat-free mass was maintained. IHTG content was significantly reduced in the Dapa than in the Con (P = 0.033). Changes in AAs showed small differences between the groups, but only serine concentrations were significantly reduced in the Dapa. Intra-group analysis showed that positive associations were observed between changes in branched chain AA concentrations and body composition only in the Dapa.

CONCLUSIONS:

Dapagliflozin treatment causes a reduction in BM mainly by reducing fat mass. AA metabolism shows subtle changes with dapagliflozin treatment.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Inibidores do Transportador 2 de Sódio-Glicose Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Inibidores do Transportador 2 de Sódio-Glicose Idioma: En Ano de publicação: 2022 Tipo de documento: Article