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. 2024 Sep 28;23:346. doi: 10.1186/s12933-024-02434-5

Table 2.

Characteristics of noninvasive imaging techniques and scoring systems

Technique/
Scoring Name
Principle Purpose Advantages Limitations CV risk prediction
TE uses shear waves induces by an external push to measure liver stiffness. Simultaneous measurement of steatosis due to the CAP technology which is based on the ultrasound beam attenuation. Assessment of liver stiffness and liver fat

Fast and easy to perform

Non-invasive, rapid, reproducible, and highly accurate

Limited sensitivity in mild liver fibrosis due to obesity and active phase of inflammation Increased liver stiffness and higher CAP values are associated with a metabolic dysfunction which is a risk factor for CVD.
ARFI + FAT QUANTIFICATION ultrasound technology measures shear wave velocity generated by tissue displacement to determine the stiffness of the liver and the ultrasound beam attenuation and or the backscattering to quantify the steatosis Evaluation of liver stiffness and fatty liver Mounted on conventional ultrasound equipment Requires high operator skills Increased liver stiffness and higher value of ultrasound beam attenuation and or backscattering are associated with a risk of CVD. At the same time the application of this technology in the carotid artery evaluation can predict ASCVD risk
MRE Uses mechanical waves to quantitatively measure tissue elasticity Evaluation of liver fibrosis and cirrhosis High-resolution imaging with high accuracy Higher cost and high equipment requirements Early identification and surveillance of CV risk through the quantification of myocardial and vascular stiffness
MRS Utilizes chemical shift imaging to distinguish hydrogen atoms in different molecular environments Quantification of liver fat content Accurate quantification of liver fat High cost, not suitable for routine clinical use identifies metabolic derangements and delineate lipid-rich atherosclerotic plaques in the arterial vasculature
APRI assesses liver fibrosis risk based on the ratio of serum AST and platelets Screening for liver fibrosis Noninvasive, easy to perform Accuracy influenced by liver inflammation and platelet disease Fluctuations in AST and platelet levels may lead to increased inflammation and thrombotic risk
FIB-4 based on age, ALT, platelets and AST Assessment of liver fibrosis risk Simple, based on routine blood tests May not be accurate enough in early stages of disease

Score of ≥ 2.67 was a significant predictor of MACEs

A valuable predictor for AVS

NFS combines multiple serum markers and demographic characteristics Assessment of liver fibrosis risk Noninvasive and multifactorial Further validation is needed to improve accuracy Higher NFS values are associated with an increased risk of MACEs
Forns index utilizes serum cholesterol levels, platelet count, age, and GGT levels to estimate fibrosis stage identifying patients with significant or advanced liver fibrosis accurately exclude advanced fibrosis, demonstrated by high NPVs may be less reliable in the presence of certain liver conditions that affect cholesterol metabolism significant correlations with various CV risk scores
HFS incorporates age, sex, AST levels, albumin, HOMA-IR, and platelet count in its algorithm, adjusting for confounding variables like diabetes status Identifying individuals presenting with substantial or progressive hepatic fibrosis Accurately discerning the absence of advanced fibrosis, as evidenced by elevated NPVs requires validation in diverse populations and may be influenced by factors such as age and diabetes Exhibiting substantial associations with a spectrum of CV risk scores
Pericoronary FAI Measures attenuation of pericoronary fat by CT scan Assessment of cardiovascular disease risk Noninvasive, quantifiable Requires CT scan, radiation exposure Greater FAI have worse cardiovascular outcomes
CCTA Uses X-rays and computer processing to create 3D images of the coronary arteries Assessment of coronary artery disease High-resolution imaging that can detect early lesions Radiation exposure, requires the use of contrast agents Identify ASCVD

TE: transient elastography, CAP: controlled attenuation parameter, ARFI: acoustic radiation force pulse imaging, ALT: alanine transaminase, MRE: magnetic resonance elastography, MRS: magnetic resonance spectroscopy, AST: aspartate transaminase, APRI: AST to platelet ratio index, FIB-4 index: Fibrosis-4 index, NAFLD: nonalcoholic fatty liver disease, NFS: NAFLD fibrosis score, Pericoronary, FAI: Pericoronary fat attenuation index, CV risk: cardiovascular risk, CVD: cardiovascular disease, ASCVD: atherosclerotic cardiovascular disease, MACEs: major adverse cardiovascular events, AVS: aortic valve sclerosis, HFS: hepamet fibrosis score, GGT: gamma-glutamyl transferase, HOMA-IR: homeostatic model assessment for insulin resistance, NPVs: negative predictive values, CT: computed tomography, CCTA: coronary computed tomography angiography