Sarcopenic Obesity in Liver Cirrhosis: Possible Mechanism and Clinical Impact

Int J Mol Sci. 2021 Feb 15;22(4):1917. doi: 10.3390/ijms22041917.

Abstract

The picture of chronic liver diseases (CLDs) has changed considerably in recent years. One of them is the increase of non-alcoholic fatty liver disease. More and more CLD patients, even those with liver cirrhosis (LC), tend to be presenting with obesity these days. The annual rate of muscle loss increases with worsening liver reserve, and thus LC patients are more likely to complicate with sarcopenia. LC is also characterized by protein-energy malnutrition (PEM). Since the PEM in LC can be invariable, the patients probably present with sarcopenic obesity (Sa-O), which involves both sarcopenia and obesity. Currently, there is no mention of Sa-O in the guidelines; however, the rapidly increasing prevalence and poorer clinical consequences of Sa-O are recognized as an important public health problem, and the diagnostic value of Sa-O is expected to increase in the future. Sa-O involves a complex interplay of physiological mechanisms, including increased inflammatory cytokines, oxidative stress, insulin resistance, hormonal disorders, and decline of physical activity. The pathogenesis of Sa-O in LC is diverse, with a lot of perturbations in the muscle-liver-adipose tissue axis. Here, we overview the current knowledge of Sa-O, especially focusing on LC.

Keywords: clinical impact; liver cirrhosis; mechanism; sarcopenic obesity.

Publication types

  • Review

MeSH terms

  • Adipose Tissue / metabolism
  • Cytokines / metabolism
  • Dysbiosis / metabolism
  • Exercise Therapy / methods
  • Fasting
  • Humans
  • Insulin Resistance
  • Liver Cirrhosis / complications*
  • Liver Cirrhosis / diet therapy
  • Liver Cirrhosis / drug therapy
  • Liver Cirrhosis / metabolism*
  • Obesity / diet therapy
  • Obesity / drug therapy
  • Obesity / etiology*
  • Obesity / metabolism*
  • Protein-Energy Malnutrition / metabolism
  • Sarcopenia / diet therapy
  • Sarcopenia / drug therapy
  • Sarcopenia / etiology*
  • Sarcopenia / metabolism*

Substances

  • Cytokines