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首页> 外文期刊>HIV medicine >Liver stiffness reduction and serum fibrosis score improvement in HIV HIV /hepatitis C virus‐coinfected patients treated with direct‐acting antivirals
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Liver stiffness reduction and serum fibrosis score improvement in HIV HIV /hepatitis C virus‐coinfected patients treated with direct‐acting antivirals

机译:肝僵硬度降低和血清纤维化分数改善艾滋病毒艾滋病毒/丙型肝炎病毒 - 用直接作用抗病毒药治疗的患者

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Objectives Only a few studies have addressed liver stiffness dynamics after hepatitis C virus ( HCV ) treatment in patients with HIV / HCV coinfection. The aim was to evaluate the variation in liver stiffness and in serum liver fibrosis scores in HIV / HCV ‐coinfected patients before and after treatment with direct‐acting antivirals ( DAA s). Methods Liver stiffness measured using transient elastography as well as serum liver fibrosis scores [fibrosis‐4 ( FIB ‐4) score and the aspartate aminotransferase to platelet ratio index ( APRI )] were evaluated before and at 6–12?months after DAA treatment. Variation in the outcome variables was evaluated using the Wilcoxon nonparametric test. Univariate analysis and multivariate regression models were used. Results A total of 78 HIV / HCV ‐coinfected subjects were included in the study. Median values of hepatic stiffness significantly decreased after DAA treatment compared with baseline [16.8 (interquartile range ( IQR ) 10.2–27.0) kP a at baseline vs . 9.4 ( IQR 6.7–15.0) kP a after DAA treatment; P? ? 0.01). Further, a decrease in median FIB ‐4 score [2.8 ( IQR 1.5–4.8) vs . 2.0 ( IQR 1.3–3.2), respectively; P? ? 0.01] and APRI [0.9 ( IQR 0.5–2.2) vs . 0.4 ( IQR 0.2–0.7), respectively; P? ? 0.01] was found. In univariate analysis, liver stiffness decrease was associated with increasing age, ‘other’ HCV genotype ( vs . G1), the presence of cirrhosis, higher pre‐ DAA liver stiffness, sofosbuvir‐based regimens and longer DAA treatment (all P? ? 0.05). Multivariate regression confirmed the significance of the association only with higher baseline liver stiffness ( P? ? 0.01). Greater FIB ‐4 and APRI reductions were associated with higher respective baseline values, while the presence of hepatic steatosis correlated with lower score reduction after DAA. Conclusions A reduction in liver stiffness and an improvement in fibrosis scores were observed in HIV / HCV ‐coinfected patients soon after DAA treatment. The clinical implications of these observations need to be evaluated in larger populations with longer follow‐up.
机译:目的在肝炎病毒(HCV)治疗患者患有艾滋病毒/ HCV繁殖患者后,目的仅解决了肝脏僵硬动力学。目的是评估肝僵硬度和血清肝纤维化分数的肝脏僵硬,在用直效抗病毒(DAA S)治疗之前和之后。方法使用瞬态弹性术和血清肝纤维化分数测量的肝硬化[纤维化-4(FIB-4)得分和血小板比指数(APLI)]的肝硬化和血小板比率指数(APRI)]进行评估,在DAA治疗后6-12个月。使用Wilcoxon非参数测试评估结果变量的变化。使用单变量分析和多元回归模型。结果总共包括78个HIV / HCV-COINFECTOFECTOMET受试者。与基线相比,DAA治疗后肝硬化的中值显着降低[16.8(IQR(IQR)10.2-27.0)KP A处于基线VS。 9.4(IQR 6.7-15.0)KP A治疗后; P? &还0.01)。此外,中值FiB -4分数减少[2.8(IQR 1.5-4.8)VS。 2.0(IQR 1.3-3.2)分别; P? &还0.01]和APRI [0.9(IQR 0.5-2.2)VS。 0.4(IQR 0.2-0.7)分别; P? &还发现了0.01]。在单变量分析中,肝僵硬度降低与年龄的增加有关,“其他”HCV基因型(V1),肝硬化的存在,较高的DAA肝刚度,基于Sofosbuvir的方案和更长的DAA处理(所有P?α& ?0.05)。多变量回归证实了只有较高基线肝刚度的关联的意义(P?& 0.01)。更大的FiB -4和APRI减少与相应的基线值更高,而肝脏脂肪变性的存在与DAA后的较低分数降低相关。结论DAA治疗后,在HIV / HCV-CoInfacted患者中观察到肝僵硬度降低和纤维化分数的改善。这些观察结果的临床意义需要在更长的群体中进行评估,随着时间更长的随访。

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