Epigenetic Reprogramming of the Inflammatory Response in Obesity and Type 2 Diabetes

Biomolecules. 2022 Jul 14;12(7):982. doi: 10.3390/biom12070982.

Abstract

For the past several decades, the prevalence of obesity and type 2 diabetes (T2D) has continued to rise on a global level. The risk contributing to this pandemic implicates both genetic and environmental factors, which are functionally integrated by epigenetic mechanisms. While these conditions are accompanied by major abnormalities in fuel metabolism, evidence indicates that altered immune cell functions also play an important role in shaping of obesity and T2D phenotypes. Interestingly, these events have been shown to be determined by epigenetic mechanisms. Consistently, recent epigenome-wide association studies have demonstrated that immune cells from obese and T2D individuals feature specific epigenetic profiles when compared to those from healthy subjects. In this work, we have reviewed recent literature reporting epigenetic changes affecting the immune cell phenotype and function in obesity and T2D. We will further discuss therapeutic strategies targeting epigenetic marks for treating obesity and T2D-associated inflammation.

Keywords: EWAS; WBCs; adipocyte hypertrophy; epigenetic drug therapy; epigenetics; immune system; inflammation; obesity and type 2 diabetes.

Publication types

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

MeSH terms

  • Diabetes Mellitus, Type 2* / complications
  • Diabetes Mellitus, Type 2* / genetics
  • Epigenesis, Genetic
  • Epigenomics
  • Humans
  • Inflammation / genetics
  • Obesity / complications
  • Obesity / genetics

Grants and funding

This study was supported by Ministero dell’Istruzione, Università e Ricerca Scientifica (grants PRIN 2017-2017CPLH32 and PON “RICERCA E INNOVAZIONE” 2014–2020 E FSC-progetto IDF SHARID-ARS01_01270) and by Regione Campania POR FESR 2014–2020 Objective 1.2. Realization of Technology Platform to fight oncologic diseases (RARE PLAT NET-CUP B63D18000380007, SATIN-CUP B61C17000070007 and COEPICA-CUP B63D18000640007 Projects).