ASSOCIATION BETWEEN METABOLIC DYSFUNCTION-ASSOCIATED FATTY LIVER DISEASE AND THE DEGREE OF HEPATIC FIBROSIS ASSESSED BY FIBROTOUCH

Vũ Hà, Thị Khánh Tường Trần, Thượng Dũng Hồ

Main Article Content

Abstract

Objective: This study aimed to investigate the association between metabolic dysfunction-associated fatty liver disease (MAFLD) and liver fibrosis severity assessed by FibroTouch, and to evaluate the predictive value of non-invasive indices APRI and FIB-4 in fibrosis risk stratification. Methods: A cross-sectional study was conducted on 256 adult patients with complete data on FibroTouch, APRI, FIB-4, and MAFLD status. Patients were categorized by fibrosis stages (F0–F4). Ordinal logistic regression was used to identify factors associated with higher stages of liver fibrosis. ResultsThe mean age was 70,02 ± 8.81 years; 66% were male. The prevalence of MAFLD was 51%. The proportion of MAFLD increased with fibrosis severity, from 44% in F0-F1 to 83% in F4 (p = 0,001). Liver enzymes (ALT, AST, GGT), APRI, and FIB-4 levels significantly increased across fibrosis stages. In ordinal logistic regression, MAFLD was independently associated with higher fibrosis severity (OR = 3.07; 95% CI: 1.71–5.68; p = 0,0002). Low-risk APRI was associated with a significantly lower risk of advanced fibrosis (OR = 0,03; 95% CI: 0,001–0,50; p = 0,017). High-risk FIB-4 tended to increase fibrosis risk but did not reach statistical significance (p = 0,102). ConclusionMAFLD is a significant independent predictor of advanced liver fibrosis. APRI and FIB-4 are useful non-invasive tools for fibrosis risk stratification, especially in patients with MAFLD

Article Details

References

Fouad Y. Metabolic-associated fatty liver disease: New nomenclature and approach with hot debate. World J Hepatol. Feb 27 2023;15(2):123-128. doi:10.4254/wjh.v15.i2.123
2. Đỗ M Q, Đào Đức T, Trần TKT, Cao Đình H. Tỷ lệ bệnh gan nhiễm mỡ liên quan chuyển hóa ở bệnh nhân đái tháo đường típ 2. VMJ. 2024;doi:doi:10.51298/vmj.v534i1.8060
3. Bae S. D. W., George J., Qiao L. From MAFLD to hepatocellular carcinoma and everything in between. Chin Med J (Engl). Feb 21 2022; 135(5): 547-556. doi:10.1097/cm9. 0000000000002089
4. Liu Z., Suo C., Shi O., et al. The Health Impact of MAFLD, a Novel Disease Cluster of NAFLD, Is Amplified by the Integrated Effect of Fatty Liver Disease-Related Genetic Variants. Clin Gastroenterol Hepatol. Apr 2022;20(4):e855-e875. doi:10.1016/j.cgh.2020.12.033
5. Liu Z., Lin C., Suo C., et al. Metabolic dysfunction-associated fatty liver disease and the risk of 24 specific cancers. Metabolism. Feb 2022; 127: 154955. doi:10.1016/j.metabol.2021. 154955
6. Nguyễn Minh Đức, Lưu Xuân Phát, Tống Nguyễn Diễm Hồng. Bệnh gan nhiễm mỡ liên quan chuyển hóa: tỷ lệ và mức độ xơ hóa gan đánh giá bằng Fibroscan Tạp chí Y Dược học Phạm Ngọc Thạch. 2024;doi:DOI: 10.59715/ pntjmp.3.1.18
7. Wai C. T., Greenson J. K., Fontana R. J., et al. A simple noninvasive index can predict both significant fibrosis and cirrhosis in patients with chronic hepatitis C. Hepatology. Aug 2003; 38(2):518-26. doi:10.1053/jhep.2003.50346
8. Jin H. Y., Noh E. S., Jeong H., Hwang I. I. T. Prediction of hepatic fibrosis using the aspartate transaminase-to-platelet ratio index in children and adolescents with metabolic dysfunction-associated steatotic liver disease. BMC Pediatr. Nov 30 2024;24(1):788. doi:10.1186/s12887-024-05263-3