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Metformin in Nonalcoholic Steatohepatitis: A Randomized Controlled Trial
BACKGROUNDN Nonalcoholic steatohepatitis (NASH) is a common liver disease that can progress to cirrhosis or hepatocellular carcinoma. It is estimated that up to 3% of the Iranian population have this condition. Although the pathogenesis of NASH is incompletely understood, there is significant eviden...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Iranian Association of Gastroerterology and Hepatology
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017700/ https://www.ncbi.nlm.nih.gov/pubmed/24829630 |
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author | Kazemi, Rozana Aduli, Mohsen Sotoudeh, Masoud Malekzadeh, Reza Seddighi, Nahid Sepanlou, Sadaf Ghajarieh Merat, Shahin |
author_facet | Kazemi, Rozana Aduli, Mohsen Sotoudeh, Masoud Malekzadeh, Reza Seddighi, Nahid Sepanlou, Sadaf Ghajarieh Merat, Shahin |
author_sort | Kazemi, Rozana |
collection | PubMed |
description | BACKGROUNDN Nonalcoholic steatohepatitis (NASH) is a common liver disease that can progress to cirrhosis or hepatocellular carcinoma. It is estimated that up to 3% of the Iranian population have this condition. Although the pathogenesis of NASH is incompletely understood, there is significant evidence pointing to the importance of insulin resistance. Metformin is an oral hypoglycemic agent known to improve insulin resistance. This study examines the effectiveness of metformin on biochemical and histological improvement among NASH patients in a randomized double-blind controlled trial. METHODS This study enrolled 33 biopsy-proven NASH patients. Other causes of liver disorders were excluded. Subjects were randomized to receive either metformin, 500 mg twice daily, or an identical-looking placebo. Overweight patients were also instructed to lose weight. Treatment continued for 6 months. Patients were regularly visited and liver enzyme levels recorded. Compliance and any adverse drug effects were recorded. RESULTS In the metformin group, the mean aspartate aminotransferase (AST) level dropped from 61.2 IU/L to 32.7 IU/L and the mean alanine aminotransferase (ALT) level dropped from 85.1 IU/L to 50.8 IU/L. The mean AST level in the placebo group dropped from 54.3 IU/L to 37.9 IU/L, whereas the mean ALT level dropped from 111.8 IU/L to 55.4 IU/L in the placebo group. The decrease in liver enzymes was significant in both groups, but the magnitude of decrease was not significantly different. CONCLUSION The improvement observed in liver enzyme levels is totally attributable to weight loss. Metformin had no significant effect on liver enzyme levels. |
format | Online Article Text |
id | pubmed-4017700 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Iranian Association of Gastroerterology and Hepatology |
record_format | MEDLINE/PubMed |
spelling | pubmed-40177002014-05-14 Metformin in Nonalcoholic Steatohepatitis: A Randomized Controlled Trial Kazemi, Rozana Aduli, Mohsen Sotoudeh, Masoud Malekzadeh, Reza Seddighi, Nahid Sepanlou, Sadaf Ghajarieh Merat, Shahin Middle East J Dig Dis Original Article BACKGROUNDN Nonalcoholic steatohepatitis (NASH) is a common liver disease that can progress to cirrhosis or hepatocellular carcinoma. It is estimated that up to 3% of the Iranian population have this condition. Although the pathogenesis of NASH is incompletely understood, there is significant evidence pointing to the importance of insulin resistance. Metformin is an oral hypoglycemic agent known to improve insulin resistance. This study examines the effectiveness of metformin on biochemical and histological improvement among NASH patients in a randomized double-blind controlled trial. METHODS This study enrolled 33 biopsy-proven NASH patients. Other causes of liver disorders were excluded. Subjects were randomized to receive either metformin, 500 mg twice daily, or an identical-looking placebo. Overweight patients were also instructed to lose weight. Treatment continued for 6 months. Patients were regularly visited and liver enzyme levels recorded. Compliance and any adverse drug effects were recorded. RESULTS In the metformin group, the mean aspartate aminotransferase (AST) level dropped from 61.2 IU/L to 32.7 IU/L and the mean alanine aminotransferase (ALT) level dropped from 85.1 IU/L to 50.8 IU/L. The mean AST level in the placebo group dropped from 54.3 IU/L to 37.9 IU/L, whereas the mean ALT level dropped from 111.8 IU/L to 55.4 IU/L in the placebo group. The decrease in liver enzymes was significant in both groups, but the magnitude of decrease was not significantly different. CONCLUSION The improvement observed in liver enzyme levels is totally attributable to weight loss. Metformin had no significant effect on liver enzyme levels. Iranian Association of Gastroerterology and Hepatology 2012-01 /pmc/articles/PMC4017700/ /pubmed/24829630 Text en © 2012 by Middle East Journal of Digestive Diseases This work is published by Middle East Journal of Digestive Diseases as an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-sa/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited. |
spellingShingle | Original Article Kazemi, Rozana Aduli, Mohsen Sotoudeh, Masoud Malekzadeh, Reza Seddighi, Nahid Sepanlou, Sadaf Ghajarieh Merat, Shahin Metformin in Nonalcoholic Steatohepatitis: A Randomized Controlled Trial |
title | Metformin in Nonalcoholic Steatohepatitis: A Randomized Controlled Trial |
title_full | Metformin in Nonalcoholic Steatohepatitis: A Randomized Controlled Trial |
title_fullStr | Metformin in Nonalcoholic Steatohepatitis: A Randomized Controlled Trial |
title_full_unstemmed | Metformin in Nonalcoholic Steatohepatitis: A Randomized Controlled Trial |
title_short | Metformin in Nonalcoholic Steatohepatitis: A Randomized Controlled Trial |
title_sort | metformin in nonalcoholic steatohepatitis: a randomized controlled trial |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017700/ https://www.ncbi.nlm.nih.gov/pubmed/24829630 |
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