首页> 外文期刊>Scandinavian journal of gastroenterology. >von Willebrand factor as a novel noninvasive predictor of portal hypertension and esophageal varices in hepatitis B patients with cirrhosis
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von Willebrand factor as a novel noninvasive predictor of portal hypertension and esophageal varices in hepatitis B patients with cirrhosis

机译:von Willebrand因子可作为乙型肝炎肝硬化患者门脉高压和食管静脉曲张的新型非侵入性预测因子

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Objective. At present, there is no perfect noninvasive method to assess portal hypertension and esophageal varices. Early predicting esophageal varices can provide evidence for managing cirrhotic patients. We aimed to further investigate von Willebrand factor (vWF) as a noninvasive predictor of portal hypertension, especially of esophageal varices. Material and Methods. A total of 60 hepatitis B patients with cirrhosis and 45 healthy subjects were enrolled in this study. Levels of six markers were examined. All patients underwent hepatic venous pressure gradient (HVPG) and esophagogastroduodenoscopy. We evaluated the performance of six factors for diagnosis of portal hypertension and esophageal varices. The vWF levels in liver tissues were observed by immunohistochemistry. Correlations between the level of vWF in liver tissues and HVPG and between levels of vWF in tissues and plasma were examined. Results. Cutoff values of plasma vWF (1510.5 mU/mL and 1701 mU/mL) showed high positive predictive value (PPV, 90.2% and 87.5%) in predicting clinically significant portal hypertension and severe portal hypertension. Cutoff values of vWF (1414 mU/ml and 1990 mU/mL, PPV 90.3% and 86.3%, respectively) were provided to detect the presence and degree of esophageal varices. Linear correlations were observed between levels of vWF in liver tissues and HVPG (r(2) = 0.552, p < 0.001) and between the level of vWF in liver tissues and in plasma (r(2) = 0.461, p < 0.001). Conclusion. The vWF is a noninvasive predictor of portal hypertension and esophageal varices in hepatitis B patients with cirrhosis. Increased levels of vWF in liver tissues may induce the elevated plasma vWF levels, but molecular mechanism is needed for further study.
机译:目的。目前,尚无完善的非侵入性方法来评估门静脉高压症和食管静脉曲张。尽早预测食管静脉曲张可为肝硬化患者的治疗提供证据。我们旨在进一步研究von Willebrand因子(vWF)作为门脉高压(尤其是食管静脉曲张)的非侵入性预测因子。材料与方法。这项研究共纳入60例乙型肝炎肝硬化患者和45例健康受试者。检查了六个标记物的水平。所有患者均接受肝静脉压力梯度(HVPG)和食管胃十二指肠镜检查。我们评估了六项因素对门脉高压和食管静脉曲张的诊断性能。通过免疫组织化学观察肝组织中的vWF水平。检查了肝组织中的vWF水平与HVPG之间的关系以及组织和血浆中的vWF水平之间的相关性。结果。血浆vWF的临界值(1510.5 mU / mL和1701 mU / mL)在预测临床上显着的门脉高压和严重门脉高压时显示出较高的阳性预测值(PPV,90.2%和87.5%)。提供vWF的截断值(分别为1414 mU / ml和1990 mU / mL,PPV分别为90.3%和86.3%)以检测食管静脉曲张的存在和程度。观察到肝组织中的vWF水平与HVPG之间存在线性相关性(r(2)= 0.552,p <0.001),肝组织和血浆中的vWF水平之间具有线性相关性(r(2)= 0.461,p <0.001)。结论。 vWF是乙型肝炎肝硬化患者门脉高压和食管静脉曲张的无创预测因子。肝组织中vWF水平升高可能会导致血浆vWF水平升高,但需要进一步研究的分子机制。

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