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代谢合并症和男性性别影响直接作用抗病毒治疗 (DAA) 后慢性丙型肝炎病毒清除后的脂肪变性:受控衰减参数 (CAP) 的评估。

Metabolic comorbidities and male sex influence steatosis in chronic hepatitis C after viral eradication by direct-acting antiviral therapy (DAAs): Evaluation by the controlled attenuation parameter (CAP).

机构信息

Unit of Internal Medicine and Metabolic Disease, Fondazione Ca' Granda IRCCS Ospedale Maggiore Policlinico, Italy; Department of Pathophysiology and Transplantation, University of Milan, Italy.

Section of Gastroenterology and Hepatology, PROMISE, University of Palermo, Italy.

出版信息

Dig Liver Dis. 2021 Oct;53(10):1301-1307. doi: 10.1016/j.dld.2020.11.001. Epub 2020 Nov 17.

Abstract

BACKGROUND

Chronic hepatitis C (CHC) is associated with hepatic steatosis, related to both a direct viral action and metabolic features. Vice-versa data on hepatic steatosis after viral eradication by direct-acting antiviral agents (DAA) are undefined although the presence of metabolic alterations could strongly influence the occurrence of steatosis as in NAFLD. The controlled attenuation parameter (CAP) (FibroscanⓇ) allows the qualitative and quantitative evaluation of fatty liver.

AIM

to evaluate in patients with CHC whether hepatic steatosis diagnosed by CAP modifies after DAAs-induced sustained virologic response (SVR).

METHODS

Data were collected the day of DAAs therapy starting and six months after SVR. CAP ≥ 248 dB/m defined the presence of steatosis.

RESULTS

794 CHC SVR patients referring to 2 Italian Units were enrolled. Mean age was 64 ± 16 ys, 50% males, BMI 25.4 ± 4 kg/m, genotype type-1 in 73%, type-3 in 8%. Prevalence of hepatic steatosis at baseline was 32% by US and 46% by CAP. De novo steatosis developed in 125 (29%), resolution in 122 (30%). At multivariate analysis de novo steatosis was independently associated with male sex (OR 1.7, CI 95% 1.09-2.67; p = 0.02) and baseline BMI (for unit increase OR 1.19, CI 95%1.11-1.29; p < 0.001). Baseline BMI (for unit increase OR 0.47, CI 95% 0.25-0.89; p = 0.02) and triglycerides (for unit increase OR 0.93, CI 95% 0.87-0.99; p = 0.03) prevented steatosis resolution after therapy.

CONCLUSIONS

after SVR de novo steatosis and resolution of baseline steatosis are closely related to the presence of metabolic comorbidities.

摘要

背景

慢性丙型肝炎(CHC)与肝脂肪变性有关,这既与病毒的直接作用有关,也与代谢特征有关。相反,直接作用抗病毒药物(DAA)根除病毒后肝脂肪变性的数据尚不清楚,尽管代谢改变的存在可能会像非酒精性脂肪性肝病(NAFLD)一样强烈影响脂肪变性的发生。控制衰减参数(CAP)(Fibroscan Ⓡ)允许对脂肪肝进行定性和定量评估。

目的

在 CHC 患者中评估 CAP 诊断的肝脂肪变性是否在 DAA 诱导的持续病毒学应答(SVR)后发生改变。

方法

在开始 DAA 治疗的当天和 SVR 后 6 个月收集数据。CAP≥248dB/m 定义为存在脂肪变性。

结果

共纳入 794 例来自 2 家意大利单位的 CHC SVR 患者。平均年龄为 64±16 岁,50%为男性,BMI 为 25.4±4kg/m,基因型 1 型占 73%,3 型占 8%。基线时 US 检测肝脂肪变性的患病率为 32%,CAP 检测为 46%。125 例(29%)新发脂肪变性,122 例(30%)脂肪变性缓解。多变量分析显示,新发脂肪变性与男性(OR 1.7,95%CI 1.09-2.67;p=0.02)和基线 BMI(每增加一个单位 OR 1.19,95%CI 1.11-1.29;p<0.001)独立相关。基线 BMI(每增加一个单位 OR 0.47,95%CI 0.25-0.89;p=0.02)和甘油三酯(每增加一个单位 OR 0.93,95%CI 0.87-0.99;p=0.03)可预防治疗后脂肪变性缓解。

结论

SVR 后,新发脂肪变性和基线脂肪变性的缓解与代谢合并症的存在密切相关。

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