Type 2 Diabetes and Metformin Use Associate With Outcomes of Patients With Non-alcoholic Steatohepatitis-related, Child-Pugh A Cirrhosis
dc.contributor.author | Vilar-Gomez, Eduardo | |
dc.contributor.author | Calzadilla-Bertot, Luis | |
dc.contributor.author | Wong, Vincent Wai-Sun | |
dc.contributor.author | Castellanos, Marlen | |
dc.contributor.author | Aller-de la Fuente, Rocio | |
dc.contributor.author | Eslam, Mohammed | |
dc.contributor.author | Wong, Grace Lai-Hung | |
dc.contributor.author | George, Jacob | |
dc.contributor.author | Romero-Gomez, Manuel | |
dc.contributor.author | Adams, Leon A. | |
dc.contributor.department | Medicine, School of Medicine | en_US |
dc.date.accessioned | 2020-07-31T18:52:54Z | |
dc.date.available | 2020-07-31T18:52:54Z | |
dc.date.issued | 2020 | |
dc.description.abstract | Background & Aims Factors that affect outcomes of patients with non-alcoholic steatohepatitis (NASH) related cirrhosis are unclear. We studied associations of type 2 diabetes, levels of hemoglobin A1c (HbA1c), and use antidiabetic medications with survival and liver-related events in patients with NASH and compensated cirrhosis. Methods We collected data from 299 patients with biopsy-proven NASH with Child-Pugh A cirrhosis from tertiary hospitals in Spain, Australia, Hong Kong, and Cuba, from April 1995 through December 2016. We obtained information on presence of type 2 diabetes, level of HbA1c, and use of antidiabetic medications. Cox proportional and competing risk models were used to estimate and compare rates of transplant-free survival, hepatic decompensation, and hepatocellular carcinoma (HCC). Results Two-hundred and twelve patients had type 2 diabetes at baseline and 8/87 patients developed diabetes during a median follow-up time of 5.1 y (range, 0.5–10.0 y). A lower proportion of patients with diabetes survived the entire follow-up period (38%) than of patients with no diabetes (81%) (adjusted hazard ratio [aHR], 4.23; 95% CI, 1.93–9.29). Higher proportions of patients with diabetes also had hepatic decompensation (51% vs 26% of patients with no diabetes; aHR, 2.03; 95% CI 1.005–4.11) and HCC (25% vs 7% of patients with no diabetes; aHR, 5.42; 95% CI 1.74–16.80). Averaged annual HbA1c levels over time were not associated with outcomes. Metformin use over time was associated with a significant reduction in risk of death or liver transplantation (aHR, 0.41; 95% CI, 0.26–0.45), hepatic decompensation (aHR, 0.80; 95% CI, 0.74–0.97), and HCC (aHR, 0.78; 95% CI, 0.69–0.96). Metformin significantly reduced risk of hepatic decompensation and HCC only in subjects with HbA1c levels above 7.0% (aHR, 0.97; 95% CI, 0.95–0.99 and aHR, 0.67; 95% CI, 0.43–0.94, respectively). Conclusions In an international cohort of patients with biopsy-proven NASH and Child-Pugh A cirrhosis, type 2 diabetes increased risk of death and liver-related outcomes, including HCC. Patients who took metformin had higher rates of survival and lower rates of decompensation and HCC. | en_US |
dc.eprint.version | Author's manuscript | en_US |
dc.identifier.citation | Vilar-Gomez, E., Calzadilla-Bertot, L., Wong, V. W.-S., Castellanos, M., Fuente, R. A. la, Eslam, M., Wong, G. L.-H., George, J., Romero-Gomez, M., & Adams, L. A. (2020). Type 2 Diabetes and Metformin Use Associate With Outcomes of Patients With Non-alcoholic Steatohepatitis-related, Child-Pugh A Cirrhosis. Clinical Gastroenterology and Hepatology. https://doi.org/10.1016/j.cgh.2020.04.083 | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/23500 | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.isversionof | 10.1016/j.cgh.2020.04.083 | en_US |
dc.relation.journal | Clinical Gastroenterology and Hepatology | en_US |
dc.rights | Publisher Policy | en_US |
dc.source | Author | en_US |
dc.subject | chemoprevention | en_US |
dc.subject | glucose intolerance | en_US |
dc.subject | ascites | en_US |
dc.title | Type 2 Diabetes and Metformin Use Associate With Outcomes of Patients With Non-alcoholic Steatohepatitis-related, Child-Pugh A Cirrhosis | en_US |
dc.type | Article | en_US |