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Noninvasive Liver Fibrosis Tests in Patients with Nonalcoholic Fatty Liver Disease: An External Validation Cohort

机译:非酒精性脂肪肝疾病患者的非血液肝纤维化试验:外部验证队列

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The main aim of this study was the comparative evaluation of nonalcoholic fatty liver disease (NAFLD) fibrosis score (NFS), fibrosis 4 index (FIB-4), AST-to-Platelet Ratio Index (APRI), and enhanced liver fibrosis (ELF) test in distinguishing none/early (F0/F1) from significant/advanced (F2/F3) fibrosis in NAFLD patients, thereby providing an external validation cohort. Thirty-one patients with biopsy-proven NAFLD and 10 matched controls without NAFLD were prospectively enrolled. Serum hyaluronic acid (HA), aminoterminal propeptide of type III procollagen (PIIINP), tissue inhibitor of metallo-proteinases (TIMP)-1, and biochemical tests were measured. NFS, FIB-4, APRI, and ELF were calculated. ELF, FIB-4, and APRI, but not NFS, were higher in F2/F3 than F0/F1 group. Specifically, ELF [area under the ROC curve (AUROC): 0.86 +/- 0.10; p=0.004) and APRI (AUROC: 0.86 +/- 0.07; p=0.005], but not NFS (AUROC: 0.68 +/- 0.12; p=0.16), and FIB-4 (AUROC: 0.71 +/- 0.11; p=0.10), could similarly discriminate F0/F1 from F2/F3 stage. The sensitivity, specificity, positive predicted value (PPV), and negative predicted value (NPV) were: a) for cut-off of APRI=0.5, 85.7%, 70.8%, 46.2%, and 94.4%, respectively, and b) for cut-off of ELF=9.0, 85.7%, 83.3%, 60.0%, and 95.2%, respectively. When ln(PIIINP) or TIMP-1 were combined with APRI, the combined AUROCs could distinguish F2/F3 from F0/F1, but without significantly higher accuracy compared with APRI alone. APRI could also distinguish patients with simple steatosis from nonalcoholic steatohepatitis, and those with from those without lobular inflammation and ballooning, findings warranting further research. In conclusions: The application of ELF test and APRI can distinguish F0/F1 from F2/F3 fibrosis stages in NAFLD patients.
机译:本研究的主要目的是非酒精性脂肪肝病(NAFLD)纤维化评分(NFS),纤维化4指数(FIB-4),AST-血小板比指数(APRI)的比较评价,增强肝纤维化(ELF )在NAFLD患者中的显着/先进(F2 / F3)纤维化中区分无/早期(F0 / F1)的测试,从而提供外部验证队列。前瞻性地注册了34名活组织检查验证的NAFLD和10个匹配对照的患者。测定血清透明质酸(HA),III型PIORALLAGEN(PIIINP),金属蛋白酶组织抑制剂(TIMP)-1和生物化学测试的氨渗透肽。计算NFS,FIB-4,APRI和ELF。 ELF,FIB-4和APRI但不是NFS,F2 / F3高于F0 / F1组。具体而言,ELF [ROC曲线下的区域(AUROC):0.86 +/- 0.10; P = 0.004)和APRI(AUCOC:0.86 +/- 0.07; P = 0.005],但不是NFS(AUCOC:0.68 +/- 0.12; P = 0.16)和FIB-4(AUROC:0.71 +/- 0.11; P = 0.10),可以类似地区分F2 / F3阶段的F0 / F1。灵敏度,特异性,阳性预测值(PPV)和负预测值(NPV)为:a)用于截止的APRI = 0.5,85.7 %,70.8%,46.2%和94.4%,分别为ELF = 9.0,85.7%,83.3%,60.0%和95.2%的截止值。当LN(PIIINP)或TIMP-1与APRI合并时,组合的氧化氢可区分F2 / F3的F0 / F1,但仅与APLI的精度明显更高。 APRI还可以将患者与非酒精性脱脂性炎症的患者区分开,以及那些没有小叶炎症和膨胀的人,调查结果进一步研究。结论:ELF试验和APRI的应用可以区分NAFLD患者F2 / F3纤维化阶段的F0 / F1。

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