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Treatment of nonalcoholic fatty liver disease with dapagliflozin in non-diabetic patients
Steatosis, a condition characterized by excessive lipid deposition. Although usually a benign condition, steatosis mays progress to cirrhosis or hepatocellular carcinoma. Recent evidence suggests that SGLT2 inhibitors suppress the development of nonalcoholic steatohepatitis in humans, as well as in...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424832/ https://www.ncbi.nlm.nih.gov/pubmed/32812927 http://dx.doi.org/10.1016/j.metop.2020.100028 |
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author | Ribeiro dos Santos, Lucas Baer Filho, Ricardo |
author_facet | Ribeiro dos Santos, Lucas Baer Filho, Ricardo |
author_sort | Ribeiro dos Santos, Lucas |
collection | PubMed |
description | Steatosis, a condition characterized by excessive lipid deposition. Although usually a benign condition, steatosis mays progress to cirrhosis or hepatocellular carcinoma. Recent evidence suggests that SGLT2 inhibitors suppress the development of nonalcoholic steatohepatitis in humans, as well as in rodent models and that SGLT2 inhibitors alleviate hepatic steatosis or steatohepatitis in obese type 2 diabetic rats or mice. 14 Patients with nonalcoholic fatty liver disease used a fixed dose of 10 mg of dapagliflozin for an average of 75 days. ALT, AST, GGT, insulin, HOMA-IR, and weight levels were significantly lower after treatment. There was no significant correlation between the reduction in HOMA and the reduction in ALT values or weight reduction obtained during treatment and ALT values. |
format | Online Article Text |
id | pubmed-7424832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-74248322020-08-17 Treatment of nonalcoholic fatty liver disease with dapagliflozin in non-diabetic patients Ribeiro dos Santos, Lucas Baer Filho, Ricardo Metabol Open Original Research Paper Steatosis, a condition characterized by excessive lipid deposition. Although usually a benign condition, steatosis mays progress to cirrhosis or hepatocellular carcinoma. Recent evidence suggests that SGLT2 inhibitors suppress the development of nonalcoholic steatohepatitis in humans, as well as in rodent models and that SGLT2 inhibitors alleviate hepatic steatosis or steatohepatitis in obese type 2 diabetic rats or mice. 14 Patients with nonalcoholic fatty liver disease used a fixed dose of 10 mg of dapagliflozin for an average of 75 days. ALT, AST, GGT, insulin, HOMA-IR, and weight levels were significantly lower after treatment. There was no significant correlation between the reduction in HOMA and the reduction in ALT values or weight reduction obtained during treatment and ALT values. Elsevier 2020-02-11 /pmc/articles/PMC7424832/ /pubmed/32812927 http://dx.doi.org/10.1016/j.metop.2020.100028 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Paper Ribeiro dos Santos, Lucas Baer Filho, Ricardo Treatment of nonalcoholic fatty liver disease with dapagliflozin in non-diabetic patients |
title | Treatment of nonalcoholic fatty liver disease with dapagliflozin in non-diabetic patients |
title_full | Treatment of nonalcoholic fatty liver disease with dapagliflozin in non-diabetic patients |
title_fullStr | Treatment of nonalcoholic fatty liver disease with dapagliflozin in non-diabetic patients |
title_full_unstemmed | Treatment of nonalcoholic fatty liver disease with dapagliflozin in non-diabetic patients |
title_short | Treatment of nonalcoholic fatty liver disease with dapagliflozin in non-diabetic patients |
title_sort | treatment of nonalcoholic fatty liver disease with dapagliflozin in non-diabetic patients |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424832/ https://www.ncbi.nlm.nih.gov/pubmed/32812927 http://dx.doi.org/10.1016/j.metop.2020.100028 |
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