Prednisolone plus S-adenosil-l-methionine in severe alcoholic hepatitis
P Tkachenko, M Maevskaya, A Pavlov, I Komkova… - Hepatology …, 2016 - Springer
P Tkachenko, M Maevskaya, A Pavlov, I Komkova, C Pavlov, V Ivashkin
Hepatology international, 2016•SpringerPurpose/background Severe alcoholic hepatitis (AH) is a life-threatening liver disease with a
potential of 30–40% mortality at 1 month. While steroids remain to be a first line therapy, they
provide only about 50% survival benefit. The aim of the study was to evaluate the efficacy of
glucocorticoids plus S-adenosylmethionine (SAMe), as compared to glucocorticoids alone,
in patients with severe alcoholic hepatitis. Methods Forty patients with severe AH were
randomized in two groups and enrolled in the prospective trial. Group 1 (n= 20) patients …
potential of 30–40% mortality at 1 month. While steroids remain to be a first line therapy, they
provide only about 50% survival benefit. The aim of the study was to evaluate the efficacy of
glucocorticoids plus S-adenosylmethionine (SAMe), as compared to glucocorticoids alone,
in patients with severe alcoholic hepatitis. Methods Forty patients with severe AH were
randomized in two groups and enrolled in the prospective trial. Group 1 (n= 20) patients …
Purpose/background
Severe alcoholic hepatitis (AH) is a life-threatening liver disease with a potential of 30–40 % mortality at 1 month. While steroids remain to be a first line therapy, they provide only about 50 % survival benefit. The aim of the study was to evaluate the efficacy of glucocorticoids plus S-adenosylmethionine (SAMe), as compared to glucocorticoids alone, in patients with severe alcoholic hepatitis.
Methods
Forty patients with severe AH were randomized in two groups and enrolled in the prospective trial. Group 1 (n = 20) patients received prednisolone 40 mg/daily per os, and group 2 (n = 20) patients were managed with prednisolone 40 mg/daily per os plus SAMe 800 mg i.v. treatment. Duration was 28 days.
Results
The response rate assessed by Lille model was significantly higher in the prednisolone plus SAMe group (19 of 20; 95 %) than in the prednisolone group (13 of 20; 65 %), p = 0.044. Two (10 %) patients died, both from the prednisolone group. There were no lethal outcomes in the prednisolone plus SAMe group. The Kaplan–Meier method showed no significant differences between the two groups (p = 0.151, log-rank). Hepatorenal syndrome (HRS) occurred in 20 % in the prednisolone group (4 of 20 patients) while no HRS cases were registered in the prednisolone plus SAMe group (p = 0.035).
Conclusions
Management of severe alcoholic hepatitis with prednisolone plus SAMe was associated with better therapy response (p = 0.044) and less frequent HRS occurrence (p = 0.035). Mortality was not significantly lower in the prednisolone–SAMe group than in the prednisolone-only group at 28 days (10 vs. 0 %, p = 0.151).
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