医学
共感染
内科学
肝活检
胃肠病学
肝病
活检
丙型肝炎
阶段(地层学)
纤维化
逻辑回归
试验预测值
切断
金标准(测试)
丙型肝炎病毒
人类免疫缺陷病毒(HIV)
免疫学
病毒
生物
古生物学
物理
量子力学
作者
Richard K. Sterling,Eduardo Lissen,Nathan Clumeck,Ricard Solà,Mendes Cassia Correa,Julio Montaner,Mark Sulkowski,Francesca J. Torriani,Doug Dieterich,David L. Thomas,Diethelm Messinger,Mark Nelson
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2006-05-25
卷期号:43 (6): 1317-1325
被引量:4084
摘要
Liver biopsy remains the gold standard in the assessment of severity of liver disease. Noninvasive tests have gained popularity to predict histology in view of the associated risks of biopsy. However, many models include tests not readily available, and there are limited data from patients with HIV/hepatitis C virus (HCV) coinfection. We aimed to develop a model using routine tests to predict liver fibrosis in patients with HIV/HCV coinfection. A retrospective analysis of liver histology was performed in 832 patients. Liver fibrosis was assessed via Ishak score; patients were categorized as 0–1, 2–3, or 4–6 and were randomly assigned to training (n = 555) or validation (n = 277) sets. Multivariate logistic regression analysis revealed that platelet count (PLT), age, AST, and INR were significantly associated with fibrosis. Additional analysis revealed PLT, age, AST, and ALT as an alternative model. Based on this, a simple index (FIB-4) was developed: age ([yr] × AST [U/L]) / ((PLT [109/L]) × (ALT [U/L])1/2). The AUROC of the index was 0.765 for differentiation between Ishak stage 0–3 and 4–6. At a cutoff of <1.45 in the validation set, the negative predictive value to exclude advanced fibrosis (stage 4–6) was 90% with a sensitivity of 70%. A cutoff of >3.25 had a positive predictive value of 65% and a specificity of 97%. Using these cutoffs, 87% of the 198 patients with FIB-4 values outside 1.45–3.25 would be correctly classified, and liver biopsy could be avoided in 71% of the validation group. In conclusion, noninvasive tests can accurately predict hepatic fibrosis and may reduce the need for liver biopsy in the majority of HIV/HCV-coinfected patients. (HEPATOLOGY 2006;43:1317–1325.)
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