LECT2, A Novel and Direct Biomarker of Liver Fibrosis in Patients With CHB.
LECT2, A Novel and Direct Biomarker of Liver Fibrosis in Patients With CHB.
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LECT2,慢性乙型肝炎患者肝纤维化的新型直接生物标志物
DOI:
10.3389/fmolb.2021.749648
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发表时间:
2021
影响因子:
5
通讯作者:
Gao Y
中科院分区:
文献类型:
--
作者:
Xu H;Li X;Wu Z;Zhao L;Shen J;Liu J;Qin J;Shen Y;Ke J;Wei Y;Li J;Gao Y
Chronic hepatitis B (CHB) patients with severe liver fibrosis would be more likely to progress to a poorer prognosis. Treatment is considered once the liver fibrosis reaches significant liver fibrosis (≥S2). Leukocyte cell-derived chemotaxin-2 (LECT2) has been shown to contribute to liver fibrosis progression. No research has focused on the role of LECT2 in liver fibrosis in CHB patients. This study enrolled 227 CHB patients and divided them into the training group (n = 147) and validation group (n = 80), respectively. The expression of LECT2 in serum, protein and mRNA of the human liver tissues was detected to analyze the possible associations between LECT2 and liver fibrosis. A receiver operating characteristic curve (ROC) was used to estimate the efficacy of LECT2 for predicting liver fibrosis. The data showed that there was a positive relationship between LECT2 and the progression of liver fibrosis. In the training group, LECT2 was demonstrated to have better effectiveness than APRI and FIB-4. The AUC was 0.861, 0.698, and 0.734 for significant liver fibrosis, and 0.855, 0.769, and 0.752 for advanced liver fibrosis. Besides, the efficacy of LECT2 in different statuses of patients with CHB was examined and the effectiveness of LECT2 had also been confirmed in the validation group. All the results confirmed that LECT2 could act as a perfect predictor and thus offers a novel and direct biomarker to estimate liver fibrosis more accurately.
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影响因子:
13.5
作者:
L'Hermitte, Antoine;Pham, Sandrine;Couty, Jean-Pierre
通讯作者:
Couty, Jean-Pierre
影响因子:
13.5
作者:
Chen, Chi-Kuan;Yang, Ching-Yao;Kuo, Min-Liang
通讯作者:
Kuo, Min-Liang
影响因子:
29.4
作者:
MCGILL, DB;RAKELA, J;OTT, BJ
通讯作者:
OTT, BJ
影响因子:
6.4
作者:
Ong, H. T.;Tan, P. K.;Hui, K. M.
通讯作者:
Hui, K. M.
影响因子:
5
作者:
Cao, Qi;Lu, Xin;Dilsizian, Vasken
通讯作者:
Dilsizian, Vasken