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门静脉高压的非侵入性评估:新兴工具与技术

Noninvasive evaluation of portal hypertension: emerging tools and techniques.

作者信息

Snowdon V K, Guha N, Fallowfield J A

机构信息

MRC/Centre for Inflammation Research, QMRI, University of Edinburgh, Edinburgh EH16 4TJ, UK.

出版信息

Int J Hepatol. 2012;2012:691089. doi: 10.1155/2012/691089. Epub 2012 Jun 7.

DOI:10.1155/2012/691089
PMID:22720166
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3376538/
Abstract

Portal hypertension is the main cause of complications in patients with cirrhosis. However, evaluating the development and progression of portal hypertension represents a challenge for clinicians. There has been considerable focus on the potential role of noninvasive markers of portal hypertension that could be used to stratify patients with respect to the stage of portal hypertension and to monitor disease progression or treatment response in a longitudinal manner without having to undertake repeated invasive assessment. The pathogenesis of portal hypertension is increasingly understood and emerging knowledge of the vascular processes that underpin portal hypertension has paved the way for exploring novel biomarkers of vascular injury, angiogenesis, and endothelial dysfunction. In this paper we focus on the pathogenesis of portal hypertension and potential non-invasive biomarkers with particular emphasis on serum analytes.

摘要

门静脉高压是肝硬化患者并发症的主要原因。然而,评估门静脉高压的发生和进展对临床医生来说是一项挑战。人们相当关注门静脉高压非侵入性标志物的潜在作用,这些标志物可用于根据门静脉高压阶段对患者进行分层,并纵向监测疾病进展或治疗反应,而无需进行重复的侵入性评估。门静脉高压的发病机制越来越为人所理解,对支撑门静脉高压的血管过程的新认识为探索血管损伤、血管生成和内皮功能障碍的新型生物标志物铺平了道路。在本文中,我们重点关注门静脉高压的发病机制和潜在的非侵入性生物标志物,尤其着重于血清分析物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f49d/3376538/53cca8542841/IJHEP2012-691089.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f49d/3376538/f5060bb7bb55/IJHEP2012-691089.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f49d/3376538/53cca8542841/IJHEP2012-691089.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f49d/3376538/f5060bb7bb55/IJHEP2012-691089.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f49d/3376538/53cca8542841/IJHEP2012-691089.002.jpg

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本文引用的文献

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Capsule endoscopy is not as accurate as esophagogastroduodenoscopy in screening cirrhotic patients for varices.胶囊内镜在筛查肝硬化患者静脉曲张方面不如食管胃十二指肠镜准确。
Clin Gastroenterol Hepatol. 2012 Mar;10(3):254-8.e1. doi: 10.1016/j.cgh.2011.11.027. Epub 2011 Dec 8.
2
Intestinal and plasma VEGF levels in cirrhosis: the role of portal pressure.肝硬化患者肠和血浆血管内皮生长因子水平:门静脉压力的作用。
J Cell Mol Med. 2012 May;16(5):1125-33. doi: 10.1111/j.1582-4934.2011.01399.x.
3
Non invasive evaluation of portal hypertension using transient elastography.
肝脏的内源性运动与门静脉高压的严重程度相关。
World J Gastroenterol. 2020 Oct 14;26(38):5836-5848. doi: 10.3748/wjg.v26.i38.5836.
4
Ultrasound-based liver elastography: current results and future perspectives.基于超声的肝脏弹性成像:当前结果和未来展望。
Abdom Radiol (NY). 2020 Nov;45(11):3463-3472. doi: 10.1007/s00261-020-02717-x. Epub 2020 Sep 11.
5
Plasma Nogo-A and placental growth factor levels are associated with portal hypertension in patients with liver cirrhosis.血浆 Nogo-A 和胎盘生长因子水平与肝硬化患者的门静脉高压相关。
World J Gastroenterol. 2019 Jun 21;25(23):2935-2946. doi: 10.3748/wjg.v25.i23.2935.
6
Noninvasive Evaluation of Portal Hypertension Using a Supervised Learning Technique.使用监督学习技术无创评估门静脉高压症。
J Healthc Eng. 2017;2017:6183714. doi: 10.1155/2017/6183714. Epub 2017 Oct 12.
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Factors That Could Impact on Liver Fibrosis Staging by Transient Elastography.可能影响瞬时弹性成像肝脏纤维化分期的因素。
Int J Hepatol. 2015;2015:624596. doi: 10.1155/2015/624596. Epub 2015 Dec 6.
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Portal hypertension as immune mediate disease.门静脉高压作为免疫介导性疾病。
Hepat Mon. 2014 Jun 7;14(6):e18625. doi: 10.5812/hepatmon.18625. eCollection 2014 Jun.
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Novel serological neo-epitope markers of extracellular matrix proteins for the detection of portal hypertension.用于检测门静脉高压症的细胞外基质蛋白新型血清学新表位标志物。
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Features of portal hypertension are associated with major adverse events in Fontan patients: the VAST study.腔静脉高压的特征与 Fontan 患者的主要不良事件相关:VAST 研究。
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使用瞬时弹性成像技术对门静脉高压进行非侵入性评估。
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4
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5
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Elevated plasma levels of urotensin II do not correlate with systemic haemodynamics in patients with cirrhosis.在肝硬化患者中,尿皮质素 II 血浆水平升高与全身血液动力学无关。
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