Vitamin E Improves Transplant‐Free Survival and Hepatic... : Hepatology (original) (raw)

Original Articles: STEATOHEPATITIS/METABOLIC LIVER DISEASE

Vitamin E Improves Transplant‐Free Survival and Hepatic Decompensation Among Patients With Nonalcoholic Steatohepatitis and Advanced Fibrosis

Vilar‐Gomez, Eduardo1; Vuppalanchi, Raj1; Gawrieh, Samer1; Ghabril, Marwan1; Saxena, Romil2; Cummings, Oscar W.2; Chalasani, Naga*,1

1Division of Gastroenterology and HepatologyIndiana University School of MedicineIndianapolisIN

2Department of PathologyIndiana University School of MedicineIndianapolisIN

*Address Correspondence and Reprint Requests to:
Naga Chalasani, M.D., Indiana University School of Medicine, 702 Rotary Circle, Suite 225, Indianapolis, IN 46202, E‐mail: [email protected], Tel: +1‐317‐278‐0414

Abstract

Vitamin E improves liver histology in adults with nonalcoholic steatohepatitis (NASH) but not diabetes, but its impact on long‐term patient outcomes is unknown. We evaluated whether vitamin E treatment improves clinical outcomes of NASH patients with bridging fibrosis or cirrhosis. Two hundred and thirty‐six patients with biopsy‐proven NASH and bridging fibrosis or cirrhosis seen at Indiana University Medical Center between October 2004 and January 2016 were included. Ninety of them took 800 international units/day of vitamin E for ≥2 years (vitamin E users) and were propensity‐matched to 90 adults who did not take vitamin E (controls) after adjusting for fibrosis severity, age, gender, body mass index, comorbidities and their treatment, low‐density lipoprotein cholesterol, liver biochemistries, and length of follow‐up on vitamin E. Covariate‐adjusted Cox and competing risk regression models were assessed to evaluate the association between vitamin E treatment and patient outcomes. The median follow‐up was 5.62 (interquartile range [IQR], 4.3‐7.5) and 5.6 (IQR, 4‐6.9) years for vitamin E users and controls, respectively. Vitamin E users had higher adjusted transplant‐free survival (78% versus 49%, P < 0.01) and lower rates of hepatic decompensation (37% versus 62%, P = 0.04) than controls. After controlling for severity of fibrosis, calendar year of patient enrollment, and other potential confounders, vitamin E treatment decreased the risk of death or transplant (adjusted hazard ratio, 0.30; 95% confidence interval [CI], 0.12‐0.74; P < 0.01) and hepatic decompensation (adjusted sub‐HR, 0.52; 95% CI, 0.28‐0.96; P = 0.036). These benefits were evident in both those with diabetes and those without diabetes. Adjusted 10‐year cumulative probabilities of hepatocellular carcinoma, vascular events, and nonhepatic cancers were not different between vitamin E–exposed patients and controls. Conclusion: Vitamin E use was associated with improved clinical outcomes in patients with NASH and bridging fibrosis or cirrhosis.