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Impaired glucose metabolism increases risk of hepatic decompensation and death in patients with compensated hepatitis C virus-related cirrhosis.

Impaired glucose metabolism increases risk of hepatic decompensation and death in patients with compensated hepatitis C virus-related cirrhosis.

Authors :
Calzadilla-Bertot, Luis
Vilar-Gomez, Eduardo
Torres-Gonzalez, Ana
Socias-Lopez, Maray
Diago, Moises
Adams, Leon A.
Romero-Gomez, Manuel
Source :
Digestive & Liver Disease; Mar2016, Vol. 48 Issue 3, p283-290, 8p
Publication Year :
2016

Abstract

Background Glucose metabolism abnormalities frequently coexist with liver cirrhosis; however, the impact of these on liver-related outcomes has not been fully investigated. Aims We examined the influence of glucose abnormalities on overall mortality and liver-related complications in cirrhotic patients. Methods A prospective cohort of 250 subjects with compensated hepatitis C virus-related cirrhosis and without known diabetes underwent an oral glucose tolerance test and were subsequently followed for a median 201 weeks. Results At baseline, 67 (27%) had type 2 diabetes. During follow-up, 28 deaths and 55 first events of decompensation occurred. After adjustment for potential confounding covariates, overall mortality/liver transplant (sHR: 2.2, 95% CI: 1.04–4.6, P = 0.04) and hepatic decompensation events (sHR: 1.9, 95% CI: 1.05–3.3, P = 0.03) were significantly higher in diabetic patients. Subjects with a HOMA-IR >5 showed higher rates of mortality (sHR: 2.2, 95% CI: 1.03–4.8, P = 0.04). The rates of hepatic decompensation were higher in patients with HOMA-IR >3 (sHR: 1.7, 95% CI: 1.04–2.9, P = 0.03). Overall, 2h-plasma glucose was the most robust predictor of overall mortality (sHR: 2.5, 95% CI: 1.03–6, P = 0.04) and decompensation (sHR: 2.7, 95% CI: 1.4–5.5, P < 0.01). Conclusions In compensated HCV-related cirrhotic patients, diabetes and marked insulin resistance are independently associated with poorer overall survival and increased risk of hepatic decompensation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15908658
Volume :
48
Issue :
3
Database :
Supplemental Index
Journal :
Digestive & Liver Disease
Publication Type :
Academic Journal
Accession number :
112906330
Full Text :
https://doi.org/10.1016/j.dld.2015.12.002