Transjugular intrahepatic portosystemic shunt insertion improves muscle mass but not muscle function or frailty measures

Eur J Gastroenterol Hepatol. 2023 Sep 1;35(9):997-1003. doi: 10.1097/MEG.0000000000002592. Epub 2023 Jun 16.

Abstract

Introduction: Sarcopenia in cirrhosis is associated with poor outcomes. While transjugular intrahepatic portosystemic shunt (TIPS) insertion improves radiological measures of muscle mass, its impact on muscle function, performance and frailty has not been evaluated.

Methods: Patients with cirrhosis referred for TIPS were prospectively recruited and followed for 6 months. L3 CT scans were used to calculate skeletal muscle and adipose tissue parameters. Handgrip strength, Liver Frailty Index and short physical performance battery were serially monitored. Dietary intake, insulin resistance, insulin-like growth factor (IGF)-1, and immune function using QuantiFERON Monitor (QFM) were measured.

Results: Twelve patients completed the study with a mean age of 58 ± 9 years and model for end-stage liver disease score of 16 ± 5. At 6 months post-TIPS, skeletal muscle area increased from 139.33 cm 2 ± 22.72 to 154.64 ± 27.42 ( P = 0.012). Significant increases were observed in the subcutaneous fat area ( P = 0.0076) and intermuscular adipose tissue ( P = 0.041), but not muscle attenuation or visceral fat. Despite marked changes in muscle mass, no improvements were observed in handgrip strength, frailty, or physical performance. At 6 months post-TIPS, IGF-1 ( P = 0.0076) and QFM ( P = 0.006) increased compared to baseline. Nutritional intake, hepatic encephalopathy measures, insulin resistance and liver biochemistry were not significantly impacted.

Conclusion: Muscle mass increased following TIPS insertion as did IGF-1, a known driver of muscle anabolism. The lack of improvement in muscle function was unexpected and may relate to impairment in muscle quality and the effects of hyperammonaemia on muscle contractile function. Improvements in QFM, a marker of immune function, may suggest a reduction in infection susceptibility in this at-risk population and requires further evaluation.

MeSH terms

  • Aged
  • End Stage Liver Disease* / complications
  • Frailty* / complications
  • Hand Strength
  • Hepatic Encephalopathy*
  • Humans
  • Insulin Resistance*
  • Insulin-Like Growth Factor I
  • Liver Cirrhosis / complications
  • Liver Cirrhosis / surgery
  • Middle Aged
  • Portasystemic Shunt, Transjugular Intrahepatic* / adverse effects
  • Retrospective Studies
  • Severity of Illness Index
  • Treatment Outcome

Substances

  • Insulin-Like Growth Factor I