Gluud et al. [86] |
Meta-analysis |
16 randomized controlled trials including 827 patients with cirrhosis |
No benefit of BCAA in decreasing mortality. BCAA did not provide any additional benefit on HE in patients already on lactulose or neomycin, but found to be beneficial in patients on no pharmacological therapy |
Les et al. [84] |
Multicenter randomized double-blind study |
116 patients with cirrhosis treated with either BCAA or maltodextrin for 56 weeks |
Patients in BCAA group had improvement in symptoms of minimal HE and muscle mass |
Muto et al [85] |
Multicenter, randomized controlled trial |
646 patients with decompensated cirrhosis |
The incidence of primary end point significantly decreased in the BCAA group. The primary end point was a composite of death by any cause, development of liver cancer, rupture of esophageal varices, or progress of hepatic failure (event-free survival) |
Horst et al. [83] |
Randomized study |
37 hospitalized protein-intolerant patients |
BCAA administration achieved positive nitrogen balance without worsening symptoms of HE |
Marchesini et al. [75] |
Randomized double-blind study |
64 patients with cirrhosis and chronic HE |
Patients who received BCAA showed significant improvement in mental status as compared to those who received casein |