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Liver‐related long‐term outcomes of thiazolidinedione use in persons with type 2 diabetes

BACKGROUND & AIMS: Studies have described prominent histologic improvement in patients with nonalcoholic steatohepatitis (NASH) using thiazolidinedione (TZD); however, these were all short term with moderate sample size, no liver‐related long‐term outcomes could be noted. METHODS: This retrospec...

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Autores principales: Yen, Fu‐Shun, Yang, Yu‐Cih, Hwu, Chii‐Min, Wei, James C.‐C., Huang, Yi‐Hsiang, Hou, Ming‐Chih, Hsu, Chih‐Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317545/
https://www.ncbi.nlm.nih.gov/pubmed/31960563
http://dx.doi.org/10.1111/liv.14385
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author Yen, Fu‐Shun
Yang, Yu‐Cih
Hwu, Chii‐Min
Wei, James C.‐C.
Huang, Yi‐Hsiang
Hou, Ming‐Chih
Hsu, Chih‐Cheng
author_facet Yen, Fu‐Shun
Yang, Yu‐Cih
Hwu, Chii‐Min
Wei, James C.‐C.
Huang, Yi‐Hsiang
Hou, Ming‐Chih
Hsu, Chih‐Cheng
author_sort Yen, Fu‐Shun
collection PubMed
description BACKGROUND & AIMS: Studies have described prominent histologic improvement in patients with nonalcoholic steatohepatitis (NASH) using thiazolidinedione (TZD); however, these were all short term with moderate sample size, no liver‐related long‐term outcomes could be noted. METHODS: This retrospective cohort study enrolled patients with newly diagnosed type 2 diabetes mellitus (T2DM) from Taiwan's National Health Insurance Research Database between 1 January 2000 and 31 December 2013. We matched TZD users and nonusers at a 1:1 ratio through propensity score matching. This study included 5095 paired TZD users and nonusers. Cox proportional hazard models were used to compare the risks of cirrhosis, hepatic decompensation, hepatic failure and all‐cause mortality between TZD users and nonusers. The Kaplan‐Meier method was used to compare the cumulative incidence of these main outcomes. RESULTS: The incidence rates of cirrhosis, hepatic decompensation, hepatic failure and all‐cause mortality during follow‐up were 0.77 vs 1.95, 1.43 vs 1.75, 0.36 vs 0.70, and 4.89 vs 3.78 per 1000 person‐years between TZD users and nonusers. The adjusted hazard ratios of cirrhosis, hepatic decompensation, hepatic failure and all‐cause mortality were 0.39 (95% confidence interval [CI]: 0.21‐0.72), 0.86 (95% CI: 0.52‐1.44), 0.46 (95% CI: 0.18‐1.17) and 1.18 (95% CI: 0.87‐1.61) respectively. CONCLUSIONS: Our study demonstrated that TZD use could significantly lower the risk of cirrhosis. In clinical settings, TZD use might be able to improve liver‐related long‐term outcomes.
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spelling pubmed-73175452020-06-29 Liver‐related long‐term outcomes of thiazolidinedione use in persons with type 2 diabetes Yen, Fu‐Shun Yang, Yu‐Cih Hwu, Chii‐Min Wei, James C.‐C. Huang, Yi‐Hsiang Hou, Ming‐Chih Hsu, Chih‐Cheng Liver Int Metabolic & Toxic Liver Diseases BACKGROUND & AIMS: Studies have described prominent histologic improvement in patients with nonalcoholic steatohepatitis (NASH) using thiazolidinedione (TZD); however, these were all short term with moderate sample size, no liver‐related long‐term outcomes could be noted. METHODS: This retrospective cohort study enrolled patients with newly diagnosed type 2 diabetes mellitus (T2DM) from Taiwan's National Health Insurance Research Database between 1 January 2000 and 31 December 2013. We matched TZD users and nonusers at a 1:1 ratio through propensity score matching. This study included 5095 paired TZD users and nonusers. Cox proportional hazard models were used to compare the risks of cirrhosis, hepatic decompensation, hepatic failure and all‐cause mortality between TZD users and nonusers. The Kaplan‐Meier method was used to compare the cumulative incidence of these main outcomes. RESULTS: The incidence rates of cirrhosis, hepatic decompensation, hepatic failure and all‐cause mortality during follow‐up were 0.77 vs 1.95, 1.43 vs 1.75, 0.36 vs 0.70, and 4.89 vs 3.78 per 1000 person‐years between TZD users and nonusers. The adjusted hazard ratios of cirrhosis, hepatic decompensation, hepatic failure and all‐cause mortality were 0.39 (95% confidence interval [CI]: 0.21‐0.72), 0.86 (95% CI: 0.52‐1.44), 0.46 (95% CI: 0.18‐1.17) and 1.18 (95% CI: 0.87‐1.61) respectively. CONCLUSIONS: Our study demonstrated that TZD use could significantly lower the risk of cirrhosis. In clinical settings, TZD use might be able to improve liver‐related long‐term outcomes. John Wiley and Sons Inc. 2020-02-10 2020-05 /pmc/articles/PMC7317545/ /pubmed/31960563 http://dx.doi.org/10.1111/liv.14385 Text en © 2020 The Authors. Liver International published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Metabolic & Toxic Liver Diseases
Yen, Fu‐Shun
Yang, Yu‐Cih
Hwu, Chii‐Min
Wei, James C.‐C.
Huang, Yi‐Hsiang
Hou, Ming‐Chih
Hsu, Chih‐Cheng
Liver‐related long‐term outcomes of thiazolidinedione use in persons with type 2 diabetes
title Liver‐related long‐term outcomes of thiazolidinedione use in persons with type 2 diabetes
title_full Liver‐related long‐term outcomes of thiazolidinedione use in persons with type 2 diabetes
title_fullStr Liver‐related long‐term outcomes of thiazolidinedione use in persons with type 2 diabetes
title_full_unstemmed Liver‐related long‐term outcomes of thiazolidinedione use in persons with type 2 diabetes
title_short Liver‐related long‐term outcomes of thiazolidinedione use in persons with type 2 diabetes
title_sort liver‐related long‐term outcomes of thiazolidinedione use in persons with type 2 diabetes
topic Metabolic & Toxic Liver Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317545/
https://www.ncbi.nlm.nih.gov/pubmed/31960563
http://dx.doi.org/10.1111/liv.14385
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