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直接作用抗病毒药物治疗 HCV 后德雷蒂斯比值与肝细胞癌和肝脏相关死亡率风险的轨迹:长达 10 年的回顾性纵向研究。

Trajectories of De Ritis ratio with risk of hepatocellular carcinoma and liver-related mortality following direct-acting antivirals for HCV: a retrospective longitudinal study up to 10 years.

机构信息

Department of Epidemiology, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing 211166, China.

Department of Infectious Diseases, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

出版信息

Carcinogenesis. 2022 Dec 31;43(12):1190-1197. doi: 10.1093/carcin/bgac094.

Abstract

The De Ritis ratio has good diagnostic accuracy in patients with chronic viral liver disease. However, its prognostic utility has remained controversial. This study was to identify different trajectories of De Ritis ratio in those hepatitis C patients cured and analyze the relationship between trajectory groups and risk of hepatocellular carcinoma (HCC) with liver-related mortality by the retrospective cohort study. This retrospective longitudinal cohort included 1241 patients with hepatitis C who underwent antiviral therapy since follow-up in 2012. De Ritis ratio trajectories were identified by the latent class growth mixed model. Patients were grouped into subgroups by De Ritis ratio according to longitudinal trajectories. The endpoints were HCC and liver-related mortality. Three distinct trajectory groups were characterized for serum De Ritis ratio: low-stable, middle-stable and high-rising. Fifty-one HCC and 11 liver-related mortality were recorded and tracked. Compared to the low-stable group, the adjusted hazard ratios (HRs) and 95% confidence interval (CI) associated with HCC and liver-related mortality were 2.02 (1.12 to 3.63), 9.36 (3.61 to 24.29), for the middle-stable, and high-rising group, respectively. Notably, the high-rising trajectory group still had prognostic significance after adjusting for preoperative levels. Likewise, for the high-rising trajectory group of sustained virological response, the HRs (95% CI) were 2.85 (1.03 to 10.75) for HCC and liver-related mortality, and in patients with cirrhosis, the HRs (95% CI) were 3.44 (1.64 to 7.19) and 4.35 (1.27 to 14.84) in the middle-stable trajectory group and the high-rising trajectory group, respectively. The dynamic measurements of De Ritis ratio are recommended to monitor the prognosis of Hepatitis C patients.

摘要

De Ritis 比值在慢性病毒性肝病患者中有很好的诊断准确性。然而,其预后价值仍存在争议。本研究旨在确定丙型肝炎患者治愈后的 De Ritis 比值不同轨迹,并通过回顾性队列研究分析轨迹组与肝细胞癌(HCC)和肝脏相关死亡率的关系。这项回顾性纵向队列研究纳入了 1241 例自 2012 年随访以来接受抗病毒治疗的丙型肝炎患者。通过潜在类别增长混合模型确定 De Ritis 比值轨迹。根据纵向轨迹将患者按 De Ritis 比值分为亚组。终点是 HCC 和肝脏相关死亡率。血清 De Ritis 比值的特征是三种不同的轨迹组:低稳定、中稳定和高升高。记录并跟踪了 51 例 HCC 和 11 例肝脏相关死亡率。与低稳定组相比,中稳定组和高升高组与 HCC 和肝脏相关死亡率相关的调整后的危险比(HR)和 95%置信区间(CI)分别为 2.02(1.12 至 3.63)和 9.36(3.61 至 24.29)。值得注意的是,在调整术前水平后,高升高轨迹组仍具有预后意义。同样,对于持续病毒学应答的高升高轨迹组,HCC 和肝脏相关死亡率的 HR(95%CI)分别为 2.85(1.03 至 10.75),对于肝硬化患者,HR(95%CI)分别为 3.44(1.64 至 7.19)和 4.35(1.27 至 14.84)在中稳定轨迹组和高升高轨迹组中。建议动态测量 De Ritis 比值以监测丙型肝炎患者的预后。

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