The Effect of 12 Weeks of β-Hydroxy-β-Methyl-Butyrate Supplementation after Liver Transplantation: A Pilot Randomized Controlled Study

Nutrients. 2019 Sep 19;11(9):2259. doi: 10.3390/nu11092259.

Abstract

Sarcopenia is a frequent complication in liver transplant (LT) recipients. β-hydroxy-β-methyl-butyrate (HMB) has the potential to increase muscle-performance and tropism. Our study aims at evaluating the effect on muscle mass and functioning, and the safety of 12 weeks of HMB supplementation in patients after LT. This is a pilot, randomized study. Male patients undergoing LT were randomly assigned to the HMB or control group. A diet interview, anthropometry and body composition by dual energy X-ray absorptiometry (DEXA) were performed at enrollment (T0), after 12 weeks (T1) and after 12 months (T12). Twenty-two liver transplant male patients were enrolled in the study: 12 in the HMB group and 10 as the control group. At enrollment, demographic, clinical and nutritional data were similar. According to the appendicular skeletal muscle index, sarcopenia was present in 50% of patients. The appendix skeletal muscle mass index (ASMI) showed a significant increase at T1 and T12 in HMB patients, but not in controls. The mid-arm muscle-circumference and hand grip strength also increased at T1 and T12 versus T0 only in the HMB group. No side effects were reported in either group. The study showed a positive effect of HMB in the recovery of muscle mass and strength after LT. HMB supplement in patients after LT was safe and well tolerated.

Keywords: appendix skeletal muscle index; dual energy X-ray absorptiometry; liver transplantation; sarcopenia; β-hydroxy-β-methyl-butyrate.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Dietary Supplements
  • Humans
  • Liver Transplantation*
  • Middle Aged
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / pathology
  • Pilot Projects
  • Postoperative Care
  • Sarcopenia / prevention & control
  • Valerates / administration & dosage
  • Valerates / pharmacology*

Substances

  • Valerates
  • beta-hydroxyisovaleric acid