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Review
. 2021 Aug:50:101167.
doi: 10.1016/j.molmet.2021.101167. Epub 2021 Jan 15.

Imaging biomarkers of NAFLD, NASH, and fibrosis

Affiliations
Review

Imaging biomarkers of NAFLD, NASH, and fibrosis

Veeral Ajmera et al. Mol Metab. 2021 Aug.

Abstract

Background: Non-alcoholic fatty liver disease (NAFLD) is a clinicopathologic entity that requires a liver biopsy assessment to diagnose the progressive form of NAFLD called non-alcoholic steatohepatitis (NASH). Liver biopsy is invasive, subject to sampling and interobserver variability, and impractical to scale to the affected population of up to 1 billion affected individuals worldwide. Non-invasive imaging biomarkers have emerged as a key modality to address the major unmet need to diagnose, stage, and longitudinally monitor NAFLD.

Scope of review: In this review, we critically examine the use of non-invasive imaging biomarkers to diagnose NAFLD, NASH, and fibrosis stage.

Major conclusions: Ultrasound and magnetic resonance imaging (MRI) biomarkers of liver fat can diagnose NAFLD. MRI proton density fat fraction (MRI-PDFF) is better than liver biopsy, particularly for following longitudinal changes in liver fat in clinical trials. Imaging biomarkers to reliably diagnose NASH are under investigation, but when used alone, continue to have only modest diagnostic accuracy. However, the fibrosis stage has the strongest association with liver decompensation and mortality, and elastography has emerged as a reliable biomarker for liver fibrosis. We review the combination of biomarkers to risk stratify patients and identify individuals needing treatment and the implications of longitudinal changes in liver stiffness measurement.

Keywords: MR Elastography; MRI; MRI-PDFF; NAFLD; NASH; Significant fibrosis.

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Conflict of interest statement

Conflict of interest Potential conflicts of interest for Rohit Loomba: Dr. Loomba serves as a consultant or advisory board member for Bird Rock Bio, Celgene, Enanta, GRI Bio, Madrigal, Metacrine, NGM, Sanofi, Arrowhead Research, Galmed, NGM, GNI, Novo Nordisk, Merck, Siemens, Pfizer, Gilead, and Glympse Bio. His institution has received grant support from Allergan, BMS, BI, Daiichi-Sankyo Inc., Eli Lilly, Galectin, Galmed, GE, Genfit, Intercept, Janssen Inc., Madrigal, Merck, NGM, Pfizer, Prometheus, Siemens, and Sirius. He is also co-founder of Liponexus Inc.

Figures

Figure 1
Figure 1
Sequential use of FIB-4 and VCTE/MRE for risk stratification in NAFLD.

References

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