非侵入性方法在评估非酒精性脂肪性肝炎患者肝纤维化中的作用

Tran Thi Khanh Tuong Nguyen Minh Duc
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引用次数: 1

摘要

目的:肝活检是诊断NAFLD/NASH纤维化程度的金标准;然而,它是侵入性的,有严重并发症的风险。本研究旨在验证fifi4、NAFLD纤维化评分(NFS)、FibroScan和ARFI在评估NAFLD/NASH患者肝纤维化中的诊断价值。患者和方法:本研究纳入101例NASH患者。所有患者均行肝活检以进行肝纤维化组织学评估,并采用非侵入性方法评估肝纤维化,包括FIB4、NFS、FibroScan和ARFI。通过受试者工作特征(ROC)曲线确定截断值以及这些方法的诊断准确性。结果:采用Metavir评分法评价组织学肝纤维化(F0: 10例;F1: 47例;F2: 24例;F3: 17例;F4: 3例)。fifi4、NFS、FibroScan和ARFI测定的肝硬度与纤维化分期显著相关(Spearman rho: 0.32;0.51;0.56和0.54;分别为p < 0.05)。fifi4、NFS、FibroScan和ARFI诊断≥F3的AUROC分别为0.6、0.8、0.8和0.9。对≥F3的诊断,FibroScan、ARFI v/s NFS比FIB4更准确(p<0.05)。其中,NFS对≥F3的诊断敏感性最高。NFS、ARFI和TE诊断≥F3的特异性值均大于80%。结论:肝硬度与肝纤维化分期有显著相关性。对晚期纤维化的诊断,FibroScan和ARFI比NFS和FIB4更准确。NFS是筛选NASH患者晚期纤维化(≥F3)的最佳方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role Of Non-Invasive Methods In Evaluating Liver Fibrosis Of Patients With Non-Alcoholic Steatohepatitis
Objectives: Liver biopsy is the gold standard for diagnosing the extent of fibrosis in NAFLD/NASH; however, it is invasive with the risk of serious complications. This study aimed to validate the diagnostic usefulness of FIB4, NAFLD Fibrosis Score (NFS), FibroScan and ARFI in assessing liver ?brosis in patients with NAFLD/NASH. Patients and Methods: The study was carried out on 101 patients with NASH. All patients underwent a liver biopsy for histological assessment of liver fibrosis and non-invasive methods for assessment of liver fibrosis including FIB4, NFS, FibroScan, and ARFI. Cut-off values along with the diagnostic accuracy of these methods were determined by receiver-operating characteristic (ROC) curves.  Results: Histological liver fibrosis was evaluated by Metavir scoring (F0: 10 cases; F1: 47 cases; F2: 24 cases; F3: 17 cases; and F4: 3 cases). Liver stiffness determined by FIB4, NFS, FibroScan, and ARFI were significantly correlated with the fibrosis stages (Spearman rho: 0.32; 0.51; 0.56 and 0.54; p<0.05, respectively). AUROC of FIB4, NFS, FibroScan and ARFI for diagnosing ≥ F3 were 0.6, 0.8, 0.8, and 0.9, respectively. FibroScan, ARFI v/s NFS were more accurate than FIB4 for diagnosing ≥ F3 (p<0.05). Among those, NFS had the highest sensitivity for diagnoses of ≥ F3. The specificity values of NFS, ARFI and TE were greater than 80% for diagnosing ≥ F3. Conclusions: Liver stiffness determined by these methods had significantly correlated with the fibrosis stages. FibroScan and ARFI had more accurate than NFS and FIB4 in diagnosis of advanced fibrosis. NFS was the best method for screening advanced fibrosis (≥ F3) in patients with NASH.
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