TY - JOUR
T1 - Comparison of noninvasive markers of fibrosis in patients with nonalcoholic fatty liver disease
AU - NASH CLINICAL RESEARCH NETWORK
AU - Shah, Amy G.
AU - Lydecker, Alison
AU - Murray, Karen
AU - Tetri, Brent N.
AU - Contos, Melissa J.
AU - Sanyal, Arun J.
AU - Abrams, Stephanie
AU - Arceo, Diana
AU - Espinosa, Denise
AU - Fairly, Leanel
AU - McCullough, Arthur
AU - Bringman, Diane
AU - Dasarathy, Srinivasan
AU - Hawkins, Carol
AU - Liu, Yao Chang
AU - Rogers, Nicholette
AU - Stager, Margaret
AU - Edwards, Kevin
AU - Sargent, Ruth
AU - Coffey, Melissa
AU - Young, Melissa
AU - Mohan, Parvathi
AU - Nair, Kavita
AU - Abdelmalek, Manal
AU - Diehl, Anna Mae
AU - Gottfried, Marcia
AU - Guy, Cynthia
AU - Killenberg, Paul
AU - Kwan, Samantha
AU - Pan, Yi Ping
AU - Piercy, Dawn
AU - Smith, Melissa
AU - Bhimalli, Prajakta
AU - Chalasani, Naga
AU - Cummings, Oscar W.
AU - Lee, Lydia
AU - Ragozzino, Linda
AU - Vuppalanchi, Raj
AU - Scheimann, Ann
AU - Torbenson, Michael
AU - Klipsch, Ann
AU - Molleston, Jean
AU - Subbarao, Girish
AU - Barlow, Sarah
AU - Derdoy, Jose
AU - Hoffmann, Joyce
AU - King, Debra
AU - Siegner, Joan
AU - Stewart, Susan
AU - Tetri, Brent A.
N1 - Funding Information:
Funding This work was supported by grants from the National Institutes of Health to the NASH Clinical Research Network (U01DK61718, U01DK61728, U01DK61731, U01DK61732, U01DK61734, U01DK61737, U01DK61738, U01DK61730, U01DK61713).
Publisher Copyright:
© 2009 by the AGA Institute.
PY - 2009/10/1
Y1 - 2009/10/1
N2 - BACKGROUND & AIMS: There is a need for a reliable and inexpensive noninvasive marker of hepatic fibrosis in patients with nonalcoholic fatty liver disease (NAFLD). We compared the performance of the FIB4 index (based on age, aspartate aminotransferase [AST] and alanine aminotransferase [ALT] levels, and platelet counts) with 6 other non-invasive markers of fibrosis in patients with NAFLD. METHODS: Using a nation-wide database of 541 adults with NAFLD, jackknifevalidated areas under receiver operating characteristic curves (AUROC) of FIB4 and 7 other markers were compared. The sensitivity at 90% specificity, 80% positive predictive value, and 90% negative predictive values were determined along with cutoffs for advanced fibrosis. RESULTS: The median FIB4 score was 1.11 (interquartile range = 0.74 -1.67). The jackknifevalidated AUROC for FIB4 was 0.802 (95% confidence interval [CI], 0.758 - 0.847), which was higher than that of the NAFLD fibrosis score (0.768; 95% CI, 0.720 - 0.816; P = .09), Goteburg University Cirrhosis Index (0.743; 95% CI, 0.695- 0.791; P < .01), AST:ALT ratio (0.742; 95% CI, 0.690 - 0.794; P < .015), AST:platelet ratio index (0.730; 95% CI, 0.681- 0.779; P < .001), AST:platelet ratio (0.720; 95% CI, 0.669 - 0.770; P < .001), body mass index, AST:ALT, diabetes (BARD) score (0.70; P < .001), or cirrhosis discriminant score (0.666; 95% CI, 0.614 - 0.718; P < .001). For a fixed specificity of 90% (FIB4 = 1.93), the sensitivity in identifying advanced fibrosis was only 50% (95% CI, 46-55). A FIB4 ≥ 2.67 had an 80% positive predictive value and a FIB4 index ≥ 1.30 had a 90% negative predictive value. CONCLUSIONS: The FIB4 index is superior to 7 other noninvasive markers of fibrosis in patients with NAFLD; however its performance characteristics highlight the need for even better noninvasive markers.
AB - BACKGROUND & AIMS: There is a need for a reliable and inexpensive noninvasive marker of hepatic fibrosis in patients with nonalcoholic fatty liver disease (NAFLD). We compared the performance of the FIB4 index (based on age, aspartate aminotransferase [AST] and alanine aminotransferase [ALT] levels, and platelet counts) with 6 other non-invasive markers of fibrosis in patients with NAFLD. METHODS: Using a nation-wide database of 541 adults with NAFLD, jackknifevalidated areas under receiver operating characteristic curves (AUROC) of FIB4 and 7 other markers were compared. The sensitivity at 90% specificity, 80% positive predictive value, and 90% negative predictive values were determined along with cutoffs for advanced fibrosis. RESULTS: The median FIB4 score was 1.11 (interquartile range = 0.74 -1.67). The jackknifevalidated AUROC for FIB4 was 0.802 (95% confidence interval [CI], 0.758 - 0.847), which was higher than that of the NAFLD fibrosis score (0.768; 95% CI, 0.720 - 0.816; P = .09), Goteburg University Cirrhosis Index (0.743; 95% CI, 0.695- 0.791; P < .01), AST:ALT ratio (0.742; 95% CI, 0.690 - 0.794; P < .015), AST:platelet ratio index (0.730; 95% CI, 0.681- 0.779; P < .001), AST:platelet ratio (0.720; 95% CI, 0.669 - 0.770; P < .001), body mass index, AST:ALT, diabetes (BARD) score (0.70; P < .001), or cirrhosis discriminant score (0.666; 95% CI, 0.614 - 0.718; P < .001). For a fixed specificity of 90% (FIB4 = 1.93), the sensitivity in identifying advanced fibrosis was only 50% (95% CI, 46-55). A FIB4 ≥ 2.67 had an 80% positive predictive value and a FIB4 index ≥ 1.30 had a 90% negative predictive value. CONCLUSIONS: The FIB4 index is superior to 7 other noninvasive markers of fibrosis in patients with NAFLD; however its performance characteristics highlight the need for even better noninvasive markers.
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U2 - 10.1016/j.cgh.2009.05.033
DO - 10.1016/j.cgh.2009.05.033
M3 - Article
C2 - 19523535
AN - SCOPUS:70349546276
SN - 1542-3565
VL - 7
SP - 1104
EP - 1112
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
IS - 10
ER -