Non-Alcoholic Fatty Liver Disease and Bone Tissue Metabolism: Current Findings and Future Perspectives

Int J Mol Sci. 2023 May 8;24(9):8445. doi: 10.3390/ijms24098445.

Abstract

Non-alcoholic fatty liver disease (NAFLD) is reaching epidemic proportions worldwide. Moreover, the prevalence of this liver disease is expected to increase rapidly in the near future, aligning with the rise in obesity and the aging of the population. The pathogenesis of NAFLD is considered to be complex and to include the interaction between genetic, metabolic, inflammatory, and environmental factors. It is now well documented that NAFLD is linked to the other conditions common to insulin resistance, such as abnormal lipid levels, metabolic syndrome, and type 2 diabetes mellitus. Additionally, it is considered that the insulin resistance may be one of the main mechanisms determining the disturbances in both bone tissue metabolism and skeletal muscles quality and functions in patients with NAFLD. To date, the association between NAFLD and osteoporosis has been described in several studies, though it worth noting that most of them included postmenopausal women or elderly patients and originated from Asia. However, taking into account the health and economic burdens of NAFLD, and the increasing prevalence of obesity in children and adolescents worldwide, further investigation of the relationship between osteopenia, osteoporosis and sarcopenia in NAFLD, including in young and middle-aged patients, is of great importance. In addition, this will help to justify active screening and surveillance of osteopenia and osteoporosis in patients with NAFLD. In this review, we will discuss various pathophysiological mechanisms and possible biologically active molecules that may interplay between NAFLD and bone tissue metabolism.

Keywords: bone tissue metabolism; non-alcoholic fatty liver disease; osteoporosis.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Aged
  • Bone and Bones / metabolism
  • Child
  • Diabetes Mellitus, Type 2* / complications
  • Female
  • Humans
  • Insulin Resistance*
  • Middle Aged
  • Non-alcoholic Fatty Liver Disease* / metabolism
  • Osteoporosis* / complications
  • Osteoporosis* / etiology
  • Pediatric Obesity* / complications
  • Risk Factors