The Long-term Efficacy of Sodium Glucose Co-transporter 2 Inhibitor in Patients with Non-alcoholic Fatty Liver Disease.


Journal

Internal medicine (Tokyo, Japan)
ISSN: 1349-7235
Titre abrégé: Intern Med
Pays: Japan
ID NLM: 9204241

Informations de publication

Date de publication:
2019
Historique:
entrez: 17 7 2019
pubmed: 17 7 2019
medline: 2 11 2019
Statut: ppublish

Résumé

Objective Sodium glucose co-transporter 2 inhibitor (SGLT-2i), recommended for patients with type 2 diabetes, has been reported to improve the liver function test results in non-alcoholic fatty liver disease (NAFLD). However, the long-term effects of SGLT-2i on the liver function and body weight in NAFLD patients have not been fully elucidated. In this study, we investigated the long-term effects of SGLT-2i in NAFLD patients. Methods Twenty-two diabetic patients with NAFLD were enrolled in this study. We assessed the body weight, liver enzyme levels, metabolism, and glucose levels at 12 months (22 cases) and 24 months (15 cases) after the initiation of SGLT-2i. The changes in controlled attenuation parameter (CAP) and liver stiffness in 20 of the 22 patients were evaluated using transient elastography (TE) and acoustic radiation force impulse (ARFI) elastography before the initiation of treatment and 1 year later. Results Body weight and aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels were significantly decreased at 12 and 24 months after SGLT-2i treatment. The decrease in the levels of ALT at 12 and 24 months was significantly correlated with the level of ALT at the initiation of SGLT-2i (r=0.813, p=0.001 and r=0.867, p=0.0001, respectively). SGLT-2i also reduced the CAP and velocity of shear wave (Vs) values at 12 months (CAP 315.1±43.4 db/mL→293.1±27.2 db/mL, p=0.027; Vs 1.87±0.8 m/s→ 1.48±0.6 m/s, p=0.011). Conclusion SGLT-2i treatment improved the liver function test results and reduced the body weight in NAFLD patients over a period of 12-24 months. This improvement was greater in patients with higher ALT values at baseline than in those with lower values.

Identifiants

pubmed: 31308341
doi: 10.2169/internalmedicine.2566-18
pmc: PMC6702010
doi:

Substances chimiques

Sodium-Glucose Transporter 2 Inhibitors 0
Aspartate Aminotransferases EC 2.6.1.1
Alanine Transaminase EC 2.6.1.2

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1987-1992

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Auteurs

Mio Yamashima (M)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Japan.

Hisamitsu Miyaaki (H)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Japan.

Satoshi Miuma (S)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Japan.

Hidetaka Shibata (H)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Japan.

Ryu Sasaki (R)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Japan.

Masafumi Haraguchi (M)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Japan.

Masanori Fukushima (M)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Japan.

Kazuhiko Nakao (K)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Japan.

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Classifications MeSH