» Articles » PMID: 31554274

Overview of the Pathogenesis, Genetic, and Non-Invasive Clinical, Biochemical, and Scoring Methods in the Assessment of NAFLD

Overview
Publisher MDPI
Date 2019 Sep 27
PMID 31554274
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Nonalcoholic fatty liver disease (NAFLD) is the most prevalent chronic liver disease worldwide. It represents a range of disorders, including simple steatosis, nonalcoholic steatohepatitis (NASH), and liver cirrhosis, and its prevalence continues to rise. In some cases, hepatocellular carcinoma (HCC) may develop. The develop;ment of non-invasive diagnostic and screening tools is needed, in order to reduce the frequency of liver biopsies. The most promising methods are those able to exclude advanced fibrosis and quantify steatosis. In this study, new perspective markers for inflammation, oxidative stress, apoptosis, and fibrogenesis; emerging scoring models for detecting hepatic steatosis and fibrosis; and new genetic, epigenetic, and multiomic studies are discussed. As isolated biochemical parameters are not specific or sensitive enough to predict the presence of NASH and fibrosis, there is a tendency to use various markers and combine them into mathematical algorithms. Several predictive models and scoring systems have been developed. Current data suggests that panels of markers (NAFLD fibrosis score, Fib-4 score, BARD score, and others) are useful diagnostic modalities to minimize the number of liver biopsies. The review unveils pathophysiological aspects related to new trends in current non-invasive biochemical, genetic, and scoring methods, and provides insight into their diagnostic accuracies and suitability in clinical practice.

Citing Articles

Oxidative Stress and Annexin A2 Differential Expression in Free Fatty Acids-Induced Non-Alcoholic Fatty Liver Disease in HepG2 Cells.

Arruda V, Azevedo G, Granato M, Matos A, Araujo T, Guerra J Int J Mol Sci. 2024; 25(17).

PMID: 39273539 PMC: 11395542. DOI: 10.3390/ijms25179591.


SIRT1 and FOXO1 role on MASLD risk: effects of DHA-rich n-3 PUFA supplementation and exercise in aged obese female mice and in post-menopausal overweight/obese women.

Yang J, Felix-Soriano E, Martinez-Gayo A, Ibanez-Santos J, Sainz N, Martinez J J Physiol Biochem. 2024; 80(3):697-712.

PMID: 39264516 PMC: 11502560. DOI: 10.1007/s13105-024-01044-9.


Efficacy of the Mediterranean Diet Containing Different Macronutrients on Non-Alcoholic Fatty Liver Disease.

Ulucay Kestane V, Bas M Nutrients. 2024; 16(16).

PMID: 39203835 PMC: 11357554. DOI: 10.3390/nu16162699.


Application of PPAR Ligands and Nanoparticle Technology in Metabolic Steatohepatitis Treatment.

Vu H, Nguyen V, Ikenaga H, Matsubara T Biomedicines. 2024; 12(8).

PMID: 39200340 PMC: 11351628. DOI: 10.3390/biomedicines12081876.


Natural compounds proposed for the management of non-alcoholic fatty liver disease.

Merenda T, Juszczak F, Ferier E, Duez P, Patris S, Decleves A Nat Prod Bioprospect. 2024; 14(1):24.

PMID: 38556609 PMC: 10982245. DOI: 10.1007/s13659-024-00445-z.


References
1.
Mirea A, Toonen E, van den Munckhof I, Munsterman I, Tjwa E, Jaeger M . Increased proteinase 3 and neutrophil elastase plasma concentrations are associated with non-alcoholic fatty liver disease (NAFLD) and type 2 diabetes. Mol Med. 2019; 25(1):16. PMC: 6498541. DOI: 10.1186/s10020-019-0084-3. View

2.
Gonzalez-Jaramillo V, Portilla-Fernandez E, Glisic M, Voortman T, Ghanbari M, Bramer W . Epigenetics and Inflammatory Markers: A Systematic Review of the Current Evidence. Int J Inflam. 2019; 2019:6273680. PMC: 6530203. DOI: 10.1155/2019/6273680. View

3.
Katsiki N, Anagnostis P, Kotsa K, Goulis D, Mikhailidis D . Obesity, Metabolic Syndrome and the Risk of Microvascular Complications in Patients with Diabetes mellitus. Curr Pharm Des. 2019; 25(18):2051-2059. DOI: 10.2174/1381612825666190708192134. View

4.
Hu X, Li Y, Li L, Zheng Y, Lv J, Huang S . Risk factors and biomarkers of non-alcoholic fatty liver disease: an observational cross-sectional population survey. BMJ Open. 2018; 8(4):e019974. PMC: 5892783. DOI: 10.1136/bmjopen-2017-019974. View

5.
Manning P, Murphy P, Wang K, Hooker J, Wolfson T, Middleton M . Liver histology and diffusion-weighted MRI in children with nonalcoholic fatty liver disease: A MAGNET study. J Magn Reson Imaging. 2017; 46(4):1149-1158. PMC: 5568908. DOI: 10.1002/jmri.25663. View