Increased hepcidin levels and non-alcoholic fatty liver disease in obese prepubertal children: a further piece to the complex puzzle of metabolic derangements

J Pediatr Endocrinol Metab. 2021 Nov 2;35(1):39-47. doi: 10.1515/jpem-2021-0070. Print 2022 Jan 27.

Abstract

Introduction: Several studies on obese youths and adults have reported increased hepcidin levels, which seems to be related to metabolic and iron metabolism alterations. The complete mechanisms involved in hepcidin increase remain to be elucidated, and particularly its role in the development of other known complications such as Nonalcoholic Fatty Liver Disease (NAFLD). NAFLD in prepubertal children might be of special interest in understanding the underlying mechanisms.

Methods: Anthropometric measurements, liver ultrasonography, lipid profile, liver function, oxidative stress, inflammatory state, and iron metabolism were studied in 42 obese prepubertal children and 33 healthy controls. We, therefore, evaluated the presence of possible correlations between Hepcidin and the other metabolic variables, and the possible association between NAFLD and iron metabolism.

Results: Hepcidin levels were significantly increased in the obese prepubertal children (p=0.001) with significant differences between obese children with and without NAFLD (p=0.01). Blood iron was lower in obese children (p=0.009). In the obese group, a negative correlation between hepcidin and both blood iron levels (p=0.01) and LagPHASE (p=0.02) was found. In addition, a positive association between hepcidin and NAFLD (p=0.03) was detected.

Conclusions: We suggest that an increase in hepcidin levels may represent an early step in iron metabolism derangements and metabolic alterations, including NAFLD, in prepubertal obese children.

Keywords: NAFLD; hepcidin; insulin resistance; iron metabolism; obesity; oxidative stress; prepubertalchildren.

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Female
  • Hepcidins / blood*
  • Humans
  • Insulin Resistance
  • Iron / metabolism*
  • Logistic Models
  • Male
  • Non-alcoholic Fatty Liver Disease / etiology*
  • Non-alcoholic Fatty Liver Disease / metabolism
  • Pediatric Obesity / metabolism*
  • Puberty / metabolism

Substances

  • Hepcidins
  • Iron