Serum ECM1 is a promising biomarker for staging and monitoring fibrosis in patients with chronic hepatitis B.

IF 8 2区 生物学 Q1 BIOLOGY
Lian Liu, Danyan Zhang, Rong Fan, Shipeng Cheng, Jichao Yang, Liyan Ma, Zhiyang Ling, Yaguang Zhang, Jinlin Hou, Xiaomei Wang, Bing Sun, Junqi Niu
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Abstract

It is critical to assess the extent and progression of liver fibrosis for patients to receive suitable treatments, but its diagnostic methods remain unmet. Extracellular matrix protein 1 (ECM1) has previously been reported to be a key factor in the induction and progression of liver fibrosis. However, little is known about the use of ECM1 as a biomarker to evaluate fibrosis. In a CCl4-induced mouse model of liver fibrosis, the present study demonstrated that ECM1 decreased with gradually increasing fibrosis. Using biopsy as a reference, the serum ECM1 levels decreased with increasing fibrosis stage in 247 patients with liver fibrosis, but there were no significant changes between fibrosis stage 2 and stage 0-1. To improve the performance of ECM1, age, platelet count, and ECM1 concentration were combined to calculate an EPA (ECM1-platelet-age) score (ranging from 0 to 10). The areas under the receiver operating characteristic curve of the EPA scores for the detection of F⩾2, F⩾3, and F4 were 0.6801, 0.7377, and 0.8083, respectively, which showed a comparable or significantly greater diagnostic performance for assessing fibrosis than that of the AST/ALT ratio, APRI score, or FIB-4 score. In HBV patients following antiviral treatment, the dynamics of the EPA score depended on the status of liver fibrosis development. The accuracy of the EPA score in predicting fibrosis regression and progression was 66.00% and 71.43%, respectively, while that of the LSM, another useful method for monitoring hepatic fibrosis changes during treatment, was only 52.00% and 7.14%, respectively. Compared with healthy controls, there were lower levels of serum ECM1 in HBV patients and individuals with HCV infection, MAFLD, ALD, PBC, and DILI. These findings suggested that individuals with reduced ECM1 levels may have a risk of developing liver injury, and further examinations or medical care are needed. In conclusion, the ECM1-containing EPA score is a valuable noninvasive test for staging fibrosis and predicting the progression of liver fibrosis. Additionally, ECM1 alone is an indicator for distinguishing patients with liver injury from healthy controls.

血清 ECM1 是对慢性乙型肝炎患者的肝纤维化进行分期和监测的一种很有前景的生物标记物。
评估肝纤维化的程度和进展对患者接受合适的治疗至关重要,但其诊断方法仍有待开发。据报道,细胞外基质蛋白 1(ECM1)是诱导肝纤维化和肝纤维化进展的关键因素。然而,人们对使用 ECM1 作为评估肝纤维化的生物标志物知之甚少。在 CCl4 诱导的小鼠肝纤维化模型中,本研究表明 ECM1 会随着肝纤维化的逐渐加重而减少。以活检为参考,247 例肝脏纤维化患者的血清 ECM1 水平随着纤维化阶段的增加而降低,但纤维化阶段 2 与阶段 0-1 之间无明显变化。为了提高 ECM1 的性能,将年龄、血小板计数和 ECM1 浓度结合起来计算 EPA(ECM1-血小板-年龄)得分(0 至 10 分)。在检测 F⩾2、F⩾3 和 F4 时,EPA 评分的接收器操作特征曲线下面积分别为 0.6801、0.7377 和 0.8083,与 AST/ALT 比值、APRI 评分或 FIB-4 评分相比,其评估纤维化的诊断性能相当或明显更高。在接受抗病毒治疗的 HBV 患者中,EPA 评分的动态变化取决于肝纤维化的发展状况。EPA 评分预测肝纤维化消退和进展的准确率分别为 66.00% 和 71.43%,而另一种监测治疗期间肝纤维化变化的有效方法 LSM 的准确率仅为 52.00% 和 7.14%。与健康对照组相比,HBV 患者、HCV 感染者、MAFLD、ALD、PBC 和 DILI 患者的血清 ECM1 水平较低。这些发现表明,ECM1 水平降低的人可能有发生肝损伤的风险,需要进一步检查或治疗。总之,含 ECM1 的 EPA 评分是一种有价值的无创检测方法,可用于肝纤维化分期和预测肝纤维化的进展。此外,仅 ECM1 一项指标就能将肝损伤患者与健康对照组区分开来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
15.10
自引率
8.80%
发文量
2907
审稿时长
3.2 months
期刊介绍: Science China Life Sciences is a scholarly journal co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China, and it is published by Science China Press. The journal is dedicated to publishing high-quality, original research findings in both basic and applied life science research.
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