慢性丙型肝炎直接抗病毒治疗后肝脏和脾脏僵硬度的变化:一项单中心、前瞻性观察研究

GastroHep Pub Date : 2022-12-19 DOI:10.1155/2022/1374410
Ryo Sugio, Yoshiyuki Sawai, K. Fukuda, T. Igura, S. Kogita, Masahiro Ichihi, Y. Seki, Norihiko Fujita, M. Oshita, Y. Imai
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引用次数: 0

摘要

背景。剪切波弹性成像测量的肝脏和脾脏刚度分别与肝纤维化和肝静脉压力梯度有很好的相关性。的目标。探讨直接抗病毒药物(DAA)对慢性丙型肝炎患者肝、脾僵硬度的长期影响。我们进行了一项单中心前瞻性观察性研究,纳入了129例经DAA治疗获得持续病毒学应答(SVR)的慢性丙型肝炎患者。在治疗前、治疗结束(EOT)和EOT后48周和96周(分别为SVR48和SVR96),用点剪切波弹性成像测量肝脏和脾脏刚度。结果。肝脏硬度测量值(LSM)继续下降至SVR96,而脾脏硬度测量值(SSM)没有变化。在SSM 3.2 m/s的分层分析中,SSM在低SSM组(SSM <3.2 m/s, n =81)没有变化,而在高SSM组(SSM≥3.2 m/s, n =48), SSM在预处理和EOT之间显著降低,但之后没有变化。SSM被估计为临床显著门脉高压的临界值。此外,对SSM高组SSM在SVR96时SSM≥3.2 m/s范围内的危险因素进行多因素分析显示,LSM≥1.93 m/s是一个显著因素(p =0.019)。结论。这些结果表明,慢性丙型肝炎患者的DAA治疗可以长期改善肝纤维化,即使达到SVR,一些晚期肝纤维化患者可能也不会期望门脉高压的改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in Liver and Splenic Stiffness after Direct-Acting Antiviral Therapy in Chronic Hepatitis C: A Single-Centre, Prospective, Observational Study
Background. Liver and spleen stiffness measured by shear-wave elastography have been demonstrated to correlate well with liver fibrosis and hepatic venous pressure gradient, respectively. Aim. To investigate the long-term effect of direct-acting antivirals (DAA) on liver and splenic stiffness in patients with chronic hepatitis C. Methods. We conducted a single-centre prospective observational study including 129 chronic hepatitis C patients who achieved a sustained virological response (SVR) with DAA treatment. Liver and spleen stiffness were measured by point shear-wave elastography at pretreatment, end of treatment (EOT), and 48 and 96 weeks after EOT (SVR48 and SVR96, respectively). Results. Liver stiffness measurements (LSM) continued to decline to SVR96, whereas there was no change in spleen stiffness measurements (SSM). Stratified analysis at the SSM 3.2 m/s, which was estimated as the cut-off value of clinically significant portal hypertension, showed that SSM did not change in the low SSM group (SSM <3.2 m/s, n =81), whereas in the high SSM group (SSM ≥3.2 m/s, n =48), the SSM decreased significantly between pretreatment and EOT but did not change thereafter. Moreover, multivariate analysis of risk factors for the SSM remaining in the range of SSM ≥3.2 m/s at SVR96 in the high SSM group revealed that LSM ≥1.93 m/s was a significant factor (p =0.019). Conclusion. These results suggest that DAA treatment of chronic hepatitis C patients may improve liver fibrosis in the long term and some patients with advanced liver fibrosis may not expect an improvement of portal hypertension even if an SVR is achieved.
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