Ratio of von Willebrand factor to ADAMTS13 is a useful predictor of esophagogastric varices progression after sustained virologic response in patients with hepatitis C virus-related liver cirrhosis.

IF 3.9 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Satoshi Iwai, Takemi Akahane, Hiroaki Takaya, Takahiro Kubo, Fumimasa Tomooka, Akihiko Shibamoto, Junya Suzuki, Yuki Tsuji, Yukihisa Fujinaga, Norihisa Nishimura, Koh Kitagawa, Kosuke Kaji, Hideto Kawaratani, Tadashi Namisaki, Masanori Matsumoto, Hitoshi Yoshiji
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Abstract

Aim: Esophagogastric varices (EGV) are a serious complication of hepatitis C virus (HCV)-related liver cirrhosis (HCV-LC). In most cases, portal hypertension improves after a sustained virologic response (SVR) is achieved with direct-acting antiviral (DAA) treatment; however, in some cases, EGV exacerbation occurs after HCV elimination. We investigated whether von Willebrand factor (VWF) and a disintegrin-like metalloproteinase with thrombospondin type-1 motif 13 (ADAMTS13) can predict EGV progression with HCV-LC after SVR achievement.

Methods: This retrospective study enrolled 47 patients with HCV-LC who achieved an SVR after DAA treatment. Eighteen patients experienced EGV progression after the SVR was achieved (EGV progression group). Twenty-nine patients did not experience EGV progression after the SVR was achieved (non-EGV progression group). Plasma VWF antigen levels and ADAMTS13 activity were measured the day before DAA treatment.

Results: The EGV progression group had significantly higher plasma VWF antigen levels (p = 0.00331) and VWF-to-ADAMTS13 ratios (p = 0.000249) than the non-EGV progression group. Multivariate logistic regression models found that a VWF-to-ADAMTS13 ratio >2.3 was the only risk factor for EGV progression after the SVR was achieved (hazard ratio [HR], 18.4; 95% confidence interval [CI], 3.08-109; p = 0.00138). During the observation period, patients with a VWF-to-ADAMTS13 ratio >2.3 had a significantly higher cumulative incidence of EGV progression after SVR achievement than patients with a VWF-to-ADAMTS13 ratio ≤2.3 (HR, 6.4; 95% CI, 1.78-22.96; p = 0.0044).

Conclusions: The VWF-to-ADAMTS13 ratio before DAA treatment for HCV could predict EGV progression after SVR achievement.

Von Willebrand因子与ADAMTS13之比可以有效预测丙型肝炎病毒相关肝硬化患者持续病毒学应答后食管胃底静脉曲张的进展。
目的:食管胃静脉曲张(EGV)是丙型肝炎病毒(HCV)相关肝硬化(HCV-LC)的一种严重并发症。在大多数情况下,通过直接作用抗病毒药物(DAA)治疗获得持续病毒学应答(SVR)后,门静脉高压会得到改善;但在某些情况下,HCV 消除后,食管胃底静脉曲张会加重。我们研究了冯-维勒布兰德因子(VWF)和具有凝血酶原 1 型基序 13 的崩解素样金属蛋白酶(ADAMTS13)能否预测 SVR 后 HCV-LC 的 EGV 进展:这项回顾性研究共纳入了47名接受DAA治疗后获得SVR的HCV-LC患者。18名患者在获得SVR后出现了EGV进展(EGV进展组)。29 名患者在获得 SVR 后未出现 EGV 进展(非 EGV 进展组)。在DAA治疗前一天测量血浆VWF抗原水平和ADAMTS13活性:结果:EGV 进展组的血浆 VWF 抗原水平(p = 0.00331)和 VWF 与 ADAMTS13 的比率(p = 0.000249)明显高于非 EGV 进展组。多变量逻辑回归模型发现,VWF-to-ADAMTS13 比率大于 2.3 是实现 SVR 后 EGV 进展的唯一风险因素(危险比 [HR],18.4;95% 置信区间 [CI],3.08-109;p = 0.00138)。在观察期内,VWF-ADAMTS13比值大于2.3的患者在获得SVR后EGV进展的累积发生率明显高于VWF-ADAMTS13比值小于2.3的患者(HR,6.4;95% CI,1.78-22.96;P = 0.0044):结论:DAA治疗HCV前的VWF-ADAMTS13比值可预测SVR达标后的EGV进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Hepatology Research
Hepatology Research 医学-胃肠肝病学
CiteScore
8.30
自引率
14.30%
发文量
124
审稿时长
1 months
期刊介绍: Hepatology Research (formerly International Hepatology Communications) is the official journal of the Japan Society of Hepatology, and publishes original articles, reviews and short comunications dealing with hepatology. Reviews or mini-reviews are especially welcomed from those areas within hepatology undergoing rapid changes. Short communications should contain concise definitive information.
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