OBJECTIVE: To assess the ability of FibroScan (FS) and the APRI, FIB-4 and FORNS indexes to predict liver fibrosis (LF), using liver biopsy as the gold standard. METHODS: LF stage was determined in 154 patients with chronic hepatitis C virus infection using the METAVIR system. Fibroscan measurements and blood samples were taken simultaneously with biopsy. The tests were evaluated using ROC curves and the concordance, sensitivity, specificity and predictive values and likelihood ratios. RESULTS: Significantly higher LF stages were found in older patients and in those with HIV coinfection. FS and FIB-4 were able to predict significant LF> or =1 and more than 94% of patients with FS>6.7 kPas or FIB-4>1.3 had LF> or =1 in liver biopsy, with low sensitivities (63% FS; 56% Fib-4). For the detection of LF> or =2, all the tests had significant predictive capacity and between 77% and 86% of the patients with FS>6.8 kPas, APRI>0.6, FIB-4>1.4 and FORNS>5.6 had LF> or =2, with low sensitivities (70%FS; 54%APRI; 59%FIB-4; 54%FORNS). All tests had high negative predictive values (91-92%) and specificities (86-92%) in the detection of advanced fibrosis (FH=4). CONCLUSION: All tests were acceptable in predicting the presence or absence of mild fibrosis (LF> or =2) and the absence of advanced fibrosis (LF=2). However, the low or moderate agreement with liver biopsy and low sensitivities in the detection of mild fibrosis indicate that liver biopsy continues to be required when the results of other methods are discordant or indeterminate. Copyright 2009 Elsevier España, S.L. All rights reserved.
OBJECTIVE: To assess the ability of FibroScan (FS) and the APRI, FIB-4 and FORNS indexes to predict liver fibrosis (LF), using liver biopsy as the gold standard. METHODS: LF stage was determined in 154 patients with chronic hepatitis C virus infection using the METAVIR system. Fibroscan measurements and blood samples were taken simultaneously with biopsy. The tests were evaluated using ROC curves and the concordance, sensitivity, specificity and predictive values and likelihood ratios. RESULTS: Significantly higher LF stages were found in older patients and in those with HIV coinfection. FS and FIB-4 were able to predict significant LF> or =1 and more than 94% of patients with FS>6.7 kPas or FIB-4>1.3 had LF> or =1 in liver biopsy, with low sensitivities (63% FS; 56% Fib-4). For the detection of LF> or =2, all the tests had significant predictive capacity and between 77% and 86% of the patients with FS>6.8 kPas, APRI>0.6, FIB-4>1.4 and FORNS>5.6 had LF> or =2, with low sensitivities (70%FS; 54%APRI; 59%FIB-4; 54%FORNS). All tests had high negative predictive values (91-92%) and specificities (86-92%) in the detection of advanced fibrosis (FH=4). CONCLUSION: All tests were acceptable in predicting the presence or absence of mild fibrosis (LF> or =2) and the absence of advanced fibrosis (LF=2). However, the low or moderate agreement with liver biopsy and low sensitivities in the detection of mild fibrosis indicate that liver biopsy continues to be required when the results of other methods are discordant or indeterminate. Copyright 2009 Elsevier España, S.L. All rights reserved.
Authors: Mihály Sulyok; Tamás Ferenci; Mihály Makara; Gábor Horváth; János Szlávik; Zsófia Rupnik; Luca Kormos; Zsuzsanna Gerlei; Zita Sulyok; István Vályi-Nagy Journal: PeerJ Date: 2017-01-11 Impact factor: 2.984
Authors: Courtney E Zola; Meredith S Duncan; Kaku So-Armah; Kristina A Crothers; Adeel A Butt; Cynthia L Gibert; Joon Woo W Kim; Joseph K Lim; Vincent Lo Re; Hilary A Tindle; Matthew S Freiberg; Evan L Brittain Journal: Sci Rep Date: 2020-10-30 Impact factor: 4.379