This narrative review will discuss the current evidence supporting the possible application of precision or personalized medicine to the management of nonalcoholic, or "metabolic", fatty liver disease (NAFLD), based on recent progress in the understanding of the genetics and epigenetics of the disease. The prevalence of NAFLD, which can progress to cirrhosis and hepatocellular carcinoma, is constantly increasing worldwide. Accurate non-invasive predictors of liver disease progression, as well as of cardiovascular complications of NAFLD, are urgently needed. Evidence is now accumulating that the genetic and epigenetic factors involved in NAFLD development can be used to develop risk scores for liver-related complications, which may render possible to implement programs for targeted screening and surveillance of complications. Moreover, genetic and epigenetic factors identifying specific sub-phenotypes of NAFLD can predict the individual response to pharmacological therapies. Finally, we describe opportunities for gene-targeted therapeutic approaches in NAFLD, where the genetic variants represent therapeutic targets for precision therapy approaches.

Genetics and Epigenetics in the Clinic: Precision Medicine in the Management of Fatty Liver Disease / A. Cespiati, N.A. Youngson, A. Tourna, L. Valenti. - In: CURRENT PHARMACEUTICAL DESIGN. - ISSN 1381-6128. - 26:10(2020 Jan 22), pp. 998-1009.

Genetics and Epigenetics in the Clinic: Precision Medicine in the Management of Fatty Liver Disease

A. Cespiati
Primo
;
L. Valenti
Ultimo
2020

Abstract

This narrative review will discuss the current evidence supporting the possible application of precision or personalized medicine to the management of nonalcoholic, or "metabolic", fatty liver disease (NAFLD), based on recent progress in the understanding of the genetics and epigenetics of the disease. The prevalence of NAFLD, which can progress to cirrhosis and hepatocellular carcinoma, is constantly increasing worldwide. Accurate non-invasive predictors of liver disease progression, as well as of cardiovascular complications of NAFLD, are urgently needed. Evidence is now accumulating that the genetic and epigenetic factors involved in NAFLD development can be used to develop risk scores for liver-related complications, which may render possible to implement programs for targeted screening and surveillance of complications. Moreover, genetic and epigenetic factors identifying specific sub-phenotypes of NAFLD can predict the individual response to pharmacological therapies. Finally, we describe opportunities for gene-targeted therapeutic approaches in NAFLD, where the genetic variants represent therapeutic targets for precision therapy approaches.
biomarker; nonalcoholic fatty liver disease; nonalcoholic steatohepatitis; precision medicine
Settore MED/09 - Medicina Interna
22-gen-2020
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/724093
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