Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Amsterdam UMC, University of Amsterdam, The Netherlands.
Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Amsterdam UMC, University of Amsterdam, The Netherlands.
J Hepatol. 2020 Aug;73(2):252-262. doi: 10.1016/j.jhep.2020.03.036. Epub 2020 Apr 8.
BACKGROUND & AIMS: The enhanced liver fibrosis (ELF) test has been proposed for the non-invasive assessment of advanced fibrosis in patients with non-alcoholic fatty liver disease (NAFLD). We performed a systematic review to estimate the accuracy of this test against biopsy.
In this systematic review, we searched MEDLINE, Embase, Web of Science and the Cochrane Library for studies that included patients with NAFLD and that used both liver biopsy (as the reference standard) and the ELF test. Two authors independently screened the references, extracted the data and assessed the quality of included studies. Due to the variation in reported thresholds, we used a multiple thresholds random effects model for meta-analysis (diagmeta R-package).
The meta-analysis of 11 studies reporting advanced fibrosis and 5 studies reporting significant fibrosis showed that the ELF test had a sensitivity of >0.90 for excluding fibrosis at a threshold of 7.7. However, as a diagnostic test at high thresholds, the test only achieved specificity and positive predictive value >0.80 in very high prevalence settings (>50%). To achieve a specificity of 0.90 for advanced and significant fibrosis, thresholds of 10.18 (sensitivity: 0.57) and 9.86 (sensitivity: 0.55) were required, respectively.
The ELF test showed high sensitivity but limited specificity to exclude advanced and significant fibrosis at low cut-offs. The diagnostic performance of the test at higher thresholds was found to be more limited in low-prevalence settings. We conclude that clinicians should carefully consider the likely disease prevalence in their practice setting and adopt suitable test thresholds to achieve the desired performance.
The enhanced liver fibrosis test has been suggested as a non-invasive blood test to aid the diagnosis of severe liver fibrosis in patients with non-alcoholic fatty liver disease (NAFLD). Our study results showed that the test has a high negative predictive value, especially in populations with low disease prevalence (likely encountered in primary care); so, it can exclude advanced fibrosis in patients with NAFLD. However, when prevalence is low, the positive predictive value of the enhanced liver fibrosis test is low, suggesting that additional strategies may be needed to make a positive diagnosis in such settings.
增强型肝纤维化(ELF)检测法已被提议用于非酒精性脂肪性肝病(NAFLD)患者的肝纤维化程度的无创评估。我们进行了一项系统综述,旨在评估该检测法与肝活检相比的准确性。
在这项系统综述中,我们检索了 MEDLINE、Embase、Web of Science 和 Cochrane 图书馆中包含 NAFLD 患者且同时使用肝活检(作为参考标准)和 ELF 检测法的研究。两位作者独立筛选参考文献、提取数据并评估纳入研究的质量。由于报告的临界值存在差异,我们使用多个临界值随机效应模型进行荟萃分析(使用 diagmeta R 包)。
11 项研究报告了晚期纤维化,5 项研究报告了显著纤维化,对这些研究进行荟萃分析的结果显示,ELF 检测法在临界值为 7.7 时,其排除纤维化的敏感性>0.90。然而,作为高临界值的诊断检测法,该检测法仅在高患病率(>50%)的情况下实现特异性和阳性预测值>0.80。为了实现对晚期和显著纤维化的特异性为 0.90,需要分别将临界值设定为 10.18(敏感性:0.57)和 9.86(敏感性:0.55)。
ELF 检测法在低临界值时显示出高敏感性,但特异性有限,无法排除晚期和显著纤维化。在低患病率的情况下,该检测法在较高临界值时的诊断性能更受限制。我们的结论是,临床医生应仔细考虑其所在实践环境中的疾病患病率,并采用合适的临界值来实现预期的性能。
增强型肝纤维化测试被提议作为一种非侵入性血液测试,以帮助诊断非酒精性脂肪性肝病(NAFLD)患者的严重肝纤维化。我们的研究结果表明,该测试具有高阴性预测值,特别是在疾病患病率较低的人群中(可能在初级保健中遇到);因此,它可以排除 NAFLD 患者的晚期纤维化。然而,当患病率较低时,增强型肝纤维化测试的阳性预测值较低,这表明在这种情况下可能需要额外的策略来做出阳性诊断。