Abstract

Metabolic-associated fatty liver disease (MAFLD) is defined as fat accumulation in the liver in the presence of metabolic alterations. This disorder is generally asymptomatic and may progress to severe liver disease, which are linked to inflammation and/or fibrosis. MAFLD has a high prevalence (26%) and therefore a considerable number of patients are at high risk of having advanced liver disease. This document provides an overview of the most relevant serological markers in the characterization and diagnosis of MAFLD. An example is provided of a routine diagnostic algorithm that incorporates serological testing. A range of useful serological scores are currently available for the management of MAFLD patients, especially for the stratification of patients at risk of fibrosis. A large proportion of thepopulation is at risk of developing severe liver disease. The integration of non-invasive serological markers in thestratification of patients at risk for liver fibrosis may contribute to improve the control and management of MAFLD patients.

Highlights

  • Guidelines and RecommendationsGuerra-Ruiz*, Gregori Casals, Paula Iruzubieta, Marta Lalana, Alba Leis, Rosa María López, Javier Crespo and Manuel Morales-Ruiz

  • This document provides an overview of the most relevant serological markers in the characterization and diagnosis of Metabolic-associated fatty liver disease (MAFLD)

  • Metabolic-associated fatty liver disease (MAFLD), previously known as non-alcoholic fatty liver disease (NAFLD) [1] encompasses a wide spectrum of liver lesions associated with the accumulation of fat in the liver, which is known as steatosis

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Summary

Guidelines and Recommendations

Guerra-Ruiz*, Gregori Casals, Paula Iruzubieta, Marta Lalana, Alba Leis, Rosa María López, Javier Crespo and Manuel Morales-Ruiz.

Definition and introduction
Histopathology and natural history
Analytical profile and diagnosis
Steatosis scores
Other variables
Serum markers of liver fibrosis
Hyaluronic acid
Use in clinical practice
An opportunity for early diagnosis of liver disease
Findings
Conclusions
Full Text
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