Observational Study
Copyright ©The Author(s) 2022.
World J Hepatol. Aug 27, 2022; 14(8): 1633-1642
Published online Aug 27, 2022. doi: 10.4254/wjh.v14.i8.1633
Figure 1
Figure 1 Frequency of liver fibrosis risk in patients with metabolic-dysfunction-associated fatty liver disease according to fibrosis-4, nonalcoholic fatty liver disease score and aspartate aminotransferase-to-platelet ratio index, n (%). APRI: Aspartate aminotransferase-to-platelet ratio index; NAFLD: Nonalcoholic fatty liver disease; FIB-4: Fibrosis-4.
Figure 2
Figure 2 Distribution of cardiovascular risk. A: Distribution of cardiovascular risk (CVR) according to the Framingham system in patients with metabolic-dysfunction-associated fatty liver disease and risk of liver fibrosis according to fibrosis-4 (FIB-4) (n = 125); B: Distribution of CVR estimated by the Framingham system in patients with metabolic-dysfunction-associated fatty liver disease according to hepatic fibrosis estimation with transient elastography (n = 69), n (%). Degrees of fibrosis by Kpa according to METAVIR: Absent: F0; Mild–moderate: F1 and F2; Advanced: F3 and F4. CVR: Cardiovascular risk; FIB-4: Fibrosis-4.

  • Citation: Salgado Alvarez GA, Pinto Galvez SM, Garcia Mora U, Cano Contreras AD, Durán Rosas C, Priego-Parra BA, Triana Romero A, Amieva Balmori M, Roesch Dietlen F, Martinez Vazquez SE, Mendez Guerrero IO, Chi-Cervera LA, Bernal Reyes R, Martinez Roriguez LA, Icaza Chavez ME, Remes Troche JM. Higher cardiovascular risk scores and liver fibrosis risk estimated by biomarkers in patients with metabolic-dysfunction-associated fatty liver disease. World J Hepatol 2022; 14(8): 1633-1642
  • URL: https://www.wjgnet.com/1948-5182/full/v14/i8/1633.htm
  • DOI: https://dx.doi.org/10.4254/wjh.v14.i8.1633