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肝硬化中的胰岛素样生长因子系统。与肾上腺素能受体阻断后身体成分变化的关系。

The insulin like growth factor system in cirrhosis. Relation to changes in body composition following adrenoreceptor blockade.

作者信息

Bonefeld Karen, Hobolth Lise, Juul Anders, Møller Søren

机构信息

Centre of Functional and Diagnostic Imaging and Research, Section of Clinical Physiology and Nuclear Medicine, Hvidovre Hospital, Denmark.

出版信息

Growth Horm IGF Res. 2012 Dec;22(6):212-8. doi: 10.1016/j.ghir.2012.09.001. Epub 2012 Sep 30.

Abstract

OBJECTIVE

Circulating levels of IGF-I and IGFBP-3 are low in cirrhosis and are related to liver dysfunction. Metabolic disturbances include malnutrition with altered body composition and osteopenia. Since the effects of IGF-I may be associated to changes in body composition and bone mineral content (BMC) in cirrhotic patients, we investigated the relations between changes in the IGF-system and body composition and the effects of long-term alpha- and beta-blockade.

DESIGN

The study was designed as a combined cross-sectional and prospective randomised controlled study of 62 patients with cirrhosis. Twenty-three of these patients were randomised to treatment with beta- or combined alpha/beta-blocker for 3 months. Haemodynamics, body composition, and systemic and hepatic IGF-I and IGFBP-3 levels were determined in all patients. In the subgroup changes in body composition and IGF-I/IGFBP-3 levels after 3 months of beta- or combined alpha/beta-blockade were additionally examined.

RESULTS

Both the hepatic and the systemic IGF systems were suppressed and correlated with liver dysfunction and anthropometrics (p<0.05-0.001). Multivariate analyses revealed that changes in the IGF-system were determined by metabolic liver dysfunction as well as anthropometrics. In the follow-up study, hepatic venous IGF-I (p=0.05) and IGFBP-3 (p=0.02) increased after 3 months only in the group who received beta-blocker. In both groups, fat body mass increased significantly after 3 months (p=0.05-0.001).

CONCLUSIONS

In cirrhosis, the IGF-system is associated with both anthropometrics and synthetic capacity of the liver. Changes in IGF-I relate to changes in anthropometrics and there seems to be a differential effect depending on the type of adrenoreceptor blockade. Future longitudinal studies are needed to unravel these mechanisms in cirrhosis.

摘要

目的

肝硬化患者循环中胰岛素样生长因子-I(IGF-I)和胰岛素样生长因子结合蛋白-3(IGFBP-3)水平较低,且与肝功能障碍有关。代谢紊乱包括营养不良伴身体成分改变和骨质减少。由于IGF-I的作用可能与肝硬化患者身体成分和骨矿物质含量(BMC)的变化有关,我们研究了IGF系统变化与身体成分之间的关系以及长期α和β受体阻滞剂的影响。

设计

本研究设计为对62例肝硬化患者进行的横断面和前瞻性随机对照联合研究。其中23例患者被随机分配接受β受体阻滞剂或α/β受体阻滞剂联合治疗3个月。测定所有患者的血流动力学、身体成分以及全身和肝脏的IGF-I和IGFBP-3水平。在亚组中,额外检查了β受体阻滞剂或α/β受体阻滞剂联合治疗3个月后身体成分和IGF-I/IGFBP-3水平的变化。

结果

肝脏和全身的IGF系统均受到抑制,且与肝功能障碍和人体测量学相关(p<0.05 - 0.001)。多变量分析显示,IGF系统的变化由代谢性肝功能障碍以及人体测量学决定。在随访研究中,仅接受β受体阻滞剂治疗的组中,肝静脉IGF-I(p = 0.05)和IGFBP-3(p = 0.02)在3个月后升高。两组中,3个月后脂肪量均显著增加(p = 0.05 - 0.001)。

结论

在肝硬化中,IGF系统与人体测量学和肝脏合成能力均有关。IGF-I的变化与人体测量学的变化相关,并且根据肾上腺素能受体阻滞剂的类型似乎存在不同的效应。未来需要进行纵向研究以阐明肝硬化中的这些机制。

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