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尾加压素II:一种与慢性肝病和门静脉高压相关的新型血管活性介质。

Urotensin II: a novel vasoactive mediator linked to chronic liver disease and portal hypertension.

作者信息

Kemp William, Krum Henry, Colman John, Bailey Michael, Yandle Tim, Richards Mark, Roberts Stuart

机构信息

Department Gastroenterology, Alfred Hospital, Melbourne, Australia.

出版信息

Liver Int. 2007 Nov;27(9):1232-9. doi: 10.1111/j.1478-3231.2007.01539.x.

Abstract

BACKGROUND/AIMS: Urotensin II (UII) is recognised as the most potent human vasoconstrictor; however, its role in chronic liver disease (CLD) is unknown.

AIM

We sought to determine serum UII levels in CLD and explore its relationship with clinical features and outcomes of patients with CLD and portal hypertension.

METHODS

UII was analysed by radio-immunoassay on cirrhotic patients undergoing hepatic venous pressure gradient (HVPG) determination and age- and sex-matched controls. Follow-up data were prospectively recorded.

RESULTS

From 1997 to 2004, 80 patients (male/female: 74/6) underwent a total of 94 HVPG assessments. UII was higher in cirrhotic patients compared with controls (2.05+/-0.06 and 1.55+/-0.09 pmol/L, P<0.001) and was correlated with HVPG (r=+0.35, P=0.001) and severity of CLD (r=+0.6, P<0.001). UII was higher in patients who developed refractory ascites (2.45+/-0.13 vs. 1.7+/-0.12 pmol/L, P<0.001) and in those who died during the follow-up period (2.27+/-0.15 pmol/L vs. 1.95+/-0.08 pmol/L, P<0.05).

CONCLUSION

Serum UII is elevated in patients with CLD, and is associated with the severity of the underlying liver disease and the degree of portal hypertension. Baseline levels can predict future complications such as refractory ascites and patient survival.

摘要

背景/目的:尾加压素II(UII)被认为是最强效的人类血管收缩剂;然而,其在慢性肝病(CLD)中的作用尚不清楚。

目的

我们试图测定CLD患者的血清UII水平,并探讨其与CLD及门静脉高压患者的临床特征和预后的关系。

方法

采用放射免疫分析法对接受肝静脉压力梯度(HVPG)测定的肝硬化患者以及年龄和性别匹配的对照组进行UII分析。前瞻性记录随访数据。

结果

1997年至2004年,80例患者(男/女:74/6)共接受了94次HVPG评估。肝硬化患者的UII水平高于对照组(分别为2.05±0.06和1.55±0.09 pmol/L,P<0.001),且与HVPG(r=+0.35,P=0.001)及CLD严重程度(r=+0.6,P<0.001)相关。出现顽固性腹水的患者UII水平较高(2.45±0.13 vs. 1.7±0.12 pmol/L,P<0.001),随访期间死亡的患者UII水平也较高(2.27±0.15 pmol/L vs. 1.95±0.08 pmol/L,P<0.05)。

结论

CLD患者血清UII升高,且与潜在肝病的严重程度及门静脉高压程度相关。基线水平可预测未来并发症,如顽固性腹水和患者生存率。

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