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Diagnostic Value of CK-18, FGF-21, and Related Biomarker Panel in Nonalcoholic Fatty Liver Disease: A Systematic Review and Meta-Analysis

机译:CK-18,FGF-21和相关生物标志物组在非酒精性脂肪性肝病中的诊断价值:系统评价和荟萃分析

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摘要

Liver biopsy still remains the gold standard for diagnosing nonalcoholic steatohepatitis (NASH), but with limitations. There is an urgent need to develop noninvasive tests that accurately distinguish NASH from simple steatosis. The purpose of this meta-analysis was to evaluate the diagnostic value of serum biomarkers including cytokeratin 18 (CK-18), fibroblast growth factor 21 (FGF-21), and combined biomarker panel (CBP) in the diagnosis of NAFLD, especially NASH. A total of 25 studies met the inclusion criteria. Pooled sensitivity and specificity values for chosen serum markers for diagnosing NASH are as follows: CK-18 (M30), 0.75 and 0.77; CK-18 (M65), 0.71 and 0.77; FGF-21, 0.62 and 0.78; and CBP, 0.92 and 0.85. CBP demonstrated better accuracy with higher sensitivity and specificity than those tested individually. Furthermore, the AUROC of CBP was 0.94 (95% CI, 0.92–0.96), compared to CK-18 or FGF-21 assay, which showed the most significant ability to distinguish NASH from simple steatosis. The results suggest that increased circulating CK-18 and FGF-21 are associated with NASH and may be used for initial assessment, but not enough. Importantly, CBP is potentially used as accurate diagnostic tools for NASH. Further prospective designed studies are warranted to confirm our findings.
机译:肝活检仍是诊断非酒精性脂肪性肝炎(NASH)的金标准,但有其局限性。迫切需要开发能够准确区分NASH与单纯脂肪变性的非侵入性测试。这项荟萃分析的目的是评估包括细胞角蛋白18(CK-18),成纤维细胞生长因子21(FGF-21)和组合生物标志物组(CBP)在内的血清生物标志物对NAFLD,尤其是NASH的诊断价值。共有25项研究符合纳入标准。选择的用于诊断NASH的血清标志物的合并灵敏度和特异性值如下:CK-18(M30),0.75和0.77; CK-18(M65),0.71和0.77; FGF-21、0.62和0.78; CBP为0.92和0.85。与单独测试的结果相比,CBP表现出更高的准确性,更高的灵敏度和特异性。此外,与CK-18或FGF-21分析相比,CBP的AUROC为0.94(95%CI,0.92-0.96),这显示出将NASH与单纯脂肪变性区分开的最显着能力。结果表明循环CK-18和FGF-21的增加与NASH有关,可能用于初步评估,但还不够。重要的是,CBP可能被用作NASH的准确诊断工具。必须进行进一步的前瞻性设计研究,以证实我们的发现。

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