Nonalcoholic fatty liver disease and adult growth hormone deficiency: An under-recognized association?

Best Pract Res Clin Endocrinol Metab. 2023 Dec;37(6):101816. doi: 10.1016/j.beem.2023.101816. Epub 2023 Aug 16.

Abstract

Growth hormone (GH) plays an essential role not only in promoting growth in children, but also in many important metabolic processes in adults. One of the major metabolic functions of GH is its stimulatory effects on the liver in generating approximately 80% of circulating insulin-like growth factor 1 (IGF-1). Adult growth hormone deficiency (GHD) is an established clinical entity defined as a defect in endogenous GH secretion that is frequently associated with central obesity, loss of muscle mass, decreased bone mass, and impaired quality of life. Nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH) are conditions that are often under-recognized in adults with GHD, and accordingly some studies have shown that GH and IGF-1 levels are decreased in patients with NAFLD. Furthermore, it has been reported that it can progress to end-stage liver cirrhosis in some adults and children with GHD. Due to their underlying mechanisms of action, GH and IGF-1 can act on hepatocytes, macrophages, and hepatic stellate cells to mitigate progression to steatosis and fibrosis. It is, thus, important to recognize NAFLD/NASH as important complications in adult and childhood GHD. Therefore, careful and thorough evaluation of NAFLD/NASH in adults with GHD and the consideration for GH replacement therapy is crucial in these patients, together with management of other metabolic risk factors, such as obesity and dyslipidemia. This review will focus on recent reports on the role of GH and IGF-1 in the liver and its clinical significance in the regulation of hepatic function.

Keywords: IGF-1; NASH; adult growth hormone deficiency (GHD); growth hormone (GH); nonalcoholic fatty liver disease (NAFLD).

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Child
  • Dwarfism, Pituitary*
  • Growth Hormone / metabolism
  • Human Growth Hormone*
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Non-alcoholic Fatty Liver Disease*
  • Obesity
  • Quality of Life

Substances

  • Insulin-Like Growth Factor I
  • Growth Hormone
  • Human Growth Hormone