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首页> 外文期刊>BMC Gastroenterology >Diagnostic value of biochemical markers (FibroTest-FibroSURE) for the prediction of liver fibrosis in patients with non-alcoholic fatty liver disease
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Diagnostic value of biochemical markers (FibroTest-FibroSURE) for the prediction of liver fibrosis in patients with non-alcoholic fatty liver disease

机译:生化标记物(FibroTest-FibroSURE)对非酒精性脂肪肝患者肝纤维化预测的诊断价值

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Background Liver biopsy is considered as the gold standard for assessing non-alcoholic fatty liver disease (NAFLD) histologic lesions. The aim of this study was to determine the diagnostic utility of non-invasive markers of fibrosis, validated in chronic viral hepatitis and alcoholic liver disease (FibroTest, FT), in patients with NAFLD. Methods 170 patients with suspected NAFLD were prospectively included in a reference center (Group 1), 97 in a multicenter study (Group 2) and 954 blood donors as controls. Fibrosis was assessed on a 5 stage histological scale validated by Kleiner et al from F0 = none, F1 = perisinusoidal or periportal, F2 = perisinusoidal and portal/periportal, F3 = bridging and F4 = cirrhosis. Histology and the biochemical measurements were blinded to any other characteristics. The area under the ROC curves (AUROC), sensitivity (Se), specificity (Sp), positive and negative predictive values (PPV, NPV) were assessed. Results In both groups FT has elevated and not different AUROCs for the diagnosis of advanced fibrosis (F2F3F4): 0.86 (95%CI 0.77–0.91) versus 0.75 (95%CI 0.61–0.83; P = 0.10), and for F3F4: 0.92 (95%CI 0.83–0.96) versus 0.81 (95%CI 0.64–0.91; P = 0.12) in Group1 and Group 2 respectively. When the 2 groups were pooled together a FT cutoff of 0.30 had a 90% NPV for advanced fibrosis (Se 77%); a FT cutoff of 0.70 had a 73% PPV for advanced fibrosis (Sp 98%). Conclusion In patients with NAFLD, FibroTest, a simple and non-invasive quantitative estimate of liver fibrosis reliably predicts advanced fibrosis.
机译:背景技术肝活检被认为是评估非酒精性脂肪性肝病(NAFLD)组织学病变的金标准。这项研究的目的是确定在NAFLD患者中在慢性病毒性肝炎和酒精性肝病(FibroTest,FT)中验证的非侵入性纤维化标记物的诊断效用。方法前瞻性将170例疑似NAFLD患者纳入参考中心(第1组),将97例纳入多中心研究(第2组),并将954名献血者作为对照。通过Kleiner等人验证的5个阶段的组织学评分评估纤维化,从F0 =无,F1 =窦周或门静脉,F2 =窦周和门脉/门静脉,F3 =桥接和F4 =肝硬化。组织学和生化测量对任何其他特征都不了解。评估了ROC曲线下的面积(AUROC),敏感性(Se),特异性(Sp),阳性和阴性预测值(PPV,NPV)。结果在两组中,FT对晚期纤维化(F2F3F4)的诊断的AUROC升高且没有差异:0.86(95%CI 0.77-0.91)对0.75(95%CI 0.61-0.83; P = 0.10),而F3F4:0.92组1和组2分别为(95%CI 0.83–0.96)和0.81(95%CI 0.64–0.91; P = 0.12)。当将两组合并在一起时,FT截止值为0.30时晚期纤维化的NPV为90%(硒为77%)。 FT截止值为0.70时,晚期纤维化的PPV为73%(Sp 98%)。结论在FibroTest对NAFLD患者进行的肝纤维化的简单无创定量评估可以可靠地预测晚期纤维化。

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