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Systematic review of the diagnostic performance of serum markers of liver fibrosis in alcoholic liver disease

机译:系统评价肝纤维化血清标志物在酒精性肝病中的诊断作用

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Background Alcoholic liver disease (ALD) is a significant cause of death and morbidity. Detection of liver fibrosis at an early stage could provide opportunities for more optimal management. Serum markers of liver fibrosis offer an alternative to biopsy. Evidence of the performance of biomarkers in ALD is needed and a systematic review to evaluate available studies was conducted. Methods Electronic databases were searched. Studies were included if they evaluated paired samples of biopsy and serum, and presented data as sensitivity, specificity, or ROC curves. Results 15 studies were included- median participant number?=?146 (range 44–1034). Studies differed with respect to patient populations. 6 single markers were evaluated (mostly Hyaluronic Acid), and ten combined panels. Biomarkers could discriminate between people with severe fibrosis/cirrhosis with high diagnostic accuracy- HA (median AUROC 0.79 range 0.69-0.93), panels (median AUROC 0.83 range 0.38-0.95). Significant heterogeneity precluded pooling. Performance was poorer for detecting less severe fibrosis. Conclusions There are limited numbers of small studies evaluating the accuracy of biomarkers in identifying fibrosis on biopsy in ALD. Some showed promise (both HA alone and some panels) in the identification of cirrhosis/severe fibrosis and could be used to rule it out in heavy drinkers. Biomarkers less accurate with less severe fibrosis.
机译:背景技术酒精性肝病(ALD)是导致死亡和发病的重要原因。早期发现肝纤维化可提供更优化管理的机会。肝纤维化的血清标志物可替代活检。需要在ALD中使用生物标志物的证据,并进行了系统的评价以评估可用的研究。方法检索电子数据库。如果他们评估了活检和血清的配对样本,并以敏感度,特异性或ROC曲线表示数据,则将其纳入研究。结果包括15项研究-中位数参与者人数=?146(范围44–1034)。关于患者人群的研究有所不同。评估了6个单一标记(主要是透明质酸),并评估了十个组合标记。生物标记物可以以高诊断准确度区分重度纤维化/肝硬化患者-HA(中位数AUROC 0.79范围0.69-0.93),小组(中位数AUROC 0.83范围0.38-0.95)。显着的异质性阻止了合并。检测较轻的纤维化的性能较差。结论评估ALD活检中纤维化的生物标志物准确性的小型研究数量有限。有些人在鉴定肝硬化/严重纤维化中表现出了希望(包括单独使用HA和一些专家组),并且可以用来在酗酒者中将其排除。生物标志物准确性较差,纤维化程度较轻。

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