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血清生长分化因子 15 可预测丙型肝炎病毒清除后肝细胞癌的发生。

Serum growth differentiation factor 15 predicts hepatocellular carcinoma occurrence after hepatitis C virus elimination.

机构信息

Suita, Japan.

Amagasaki, Japan.

出版信息

Aliment Pharmacol Ther. 2022 Feb;55(4):422-433. doi: 10.1111/apt.16691. Epub 2021 Nov 23.

DOI:10.1111/apt.16691
PMID:34812502
Abstract

BACKGROUND

After hepatitis C virus (HCV) elimination, patients should be followed up due to risk of hepatocellular carcinoma (HCC). Growth differentiation factor 15 (GDF15) is a cytokine induced by mitochondrial dysfunction or oxidative stress. Aim To evaluate the prognostic value of GDF15 for HCC occurrence after HCV elimination.

METHODS

We measured GDF15 levels in stored serum from patients with chronic HCV infection without a history of HCC who had achieved sustained virological response with direct-acting antiviral agents (DAAs). The patients were randomly divided into derivation (n = 964) and validation (n = 642) cohorts.

RESULTS

In the derivation cohort, serum GDF15 levels were higher in those with HCC occurrence after DAA treatment than in those without. Multivariate Cox proportional hazards analysis revealed baseline GDF15 (>1350 pg/mL, HR 2.54), AFP (>5 ng/mL, HR 2.00), and the FIB-4 index (>3.25, HR 2.69) to be independent risk factors for HCC. Scoring based on GDF15, AFP and the FIB-4 index stratified HCC occurrence risk. In the validation cohort, the cumulative HCC occurrence rate at 3 years was 0.64%, 3.27% and 15.3% in low-score (N = 171), medium-score (N = 300) and high-score (N = 166) groups, respectively. In the total cohort, scoring divided patients with a FIB-4 index ≤3.25, whose HCC occurrence rate was 2.0% at 3 years, into medium-score and low-score groups with HCC occurrence rates at 3 years of 3.76% and 0.24%, respectively.

CONCLUSIONS

Serum GDF15 predicts de novo HCC occurrence. Scoring using GDF15, AFP, and the FIB-4 index can predict de novo HCC occurrence risk after HCV elimination.

摘要

背景

丙型肝炎病毒(HCV)清除后,由于肝细胞癌(HCC)的风险,患者应进行随访。生长分化因子 15(GDF15)是一种由线粒体功能障碍或氧化应激诱导的细胞因子。目的:评估 GDF15 对 HCV 清除后 HCC 发生的预后价值。

方法

我们测量了接受直接作用抗病毒药物(DAA)治疗后获得持续病毒学应答且无 HCC 病史的慢性 HCV 感染患者储存血清中的 GDF15 水平。患者被随机分为推导队列(n=964)和验证队列(n=642)。

结果

在推导队列中,与 DAA 治疗后未发生 HCC 的患者相比,发生 HCC 的患者血清 GDF15 水平更高。多变量 Cox 比例风险分析显示,基线 GDF15(>1350pg/mL,HR 2.54)、AFP(>5ng/mL,HR 2.00)和 FIB-4 指数(>3.25,HR 2.69)是 HCC 的独立危险因素。基于 GDF15、AFP 和 FIB-4 指数的评分可分层 HCC 发生风险。在验证队列中,低评分组(N=171)、中评分组(N=300)和高评分组(N=166)的 3 年 HCC 累积发生率分别为 0.64%、3.27%和 15.3%。在总队列中,评分将 FIB-4 指数≤3.25 的患者分为中评分组和低评分组,3 年 HCC 发生率分别为 3.76%和 0.24%。

结论

血清 GDF15 预测新发 HCC 的发生。使用 GDF15、AFP 和 FIB-4 指数评分可以预测 HCV 清除后新发 HCC 的发生风险。

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