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血清白蛋白水平会影响托伐普坦在肝硬化患者中的药理作用吗?日本既往临床试验的事后分析。

Can serum albumin level affect the pharmacological action of tolvaptan in patients with liver cirrhosis? A post hoc analysis of previous clinical trials in Japan.

作者信息

Sakaida Isao, Nakajima Koji, Okita Kiwamu, Hori Masatsugu, Izumi Tohru, Sakurai Masaya, Shibasaki Yoshiyuki, Tachikawa Sayaka, Tsubouchi Hidetsugu, Oka Hiromi, Kobayashi Hiroyuki

机构信息

Department of Gastroenterology and Hepatology, Yamaguchi University Graduate School of Medicine, Minami Kogushi 1-1-1, Ube, Yamaguchi, 755-8505, Japan.

Department of Medical Affairs, Otsuka Pharmaceutical Co. Ltd., Tokyo, Japan.

出版信息

J Gastroenterol. 2015 Oct;50(10):1047-53. doi: 10.1007/s00535-015-1052-5. Epub 2015 Feb 18.

DOI:10.1007/s00535-015-1052-5
PMID:25689936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4592499/
Abstract

BACKGROUND

Patients with hypoalbuminemia often fail to respond to increased doses of loop diuretics. We therefore performed a post hoc analysis to investigate the pharmacological action of tolvaptan and whether it is dependent on the serum albumin level.

METHODS

This analysis was based on four previous clinical trials of tolvaptan in patients with liver cirrhosis who exhibited insufficient response to conventional diuretics. We analyzed the correlation between the change in the initial 24-h cumulative urine volume from baseline and the serum albumin level at baseline, and assessed potential predictive factors of response to tolvaptan.

RESULTS

The correlation coefficient was 0.029 in the placebo group and -0.112 in the 7.5 mg tolvaptan group of patients with liver cirrhosis. Administration of tolvaptan provoked a stable response regardless of the serum albumin level. Tolvaptan use was identified as a significant predictor of pharmacological action, and was shown to change the initial urine volume by 885 mL (P < 0.0001) in liver cirrhosis patients.

CONCLUSIONS

In this post hoc analysis, tolvaptan increased the initial urine volume from baseline regardless of serum albumin levels. Use of tolvaptan as an add-on therapy to loop diuretics can be considered an optimal therapeutic option in patients with insufficient response to loop diuretics.

摘要

背景

低白蛋白血症患者通常对增加剂量的袢利尿剂无反应。因此,我们进行了一项事后分析,以研究托伐普坦的药理作用及其是否依赖于血清白蛋白水平。

方法

该分析基于之前四项关于托伐普坦治疗对传统利尿剂反应不足的肝硬化患者的临床试验。我们分析了基线时最初24小时累积尿量变化与基线血清白蛋白水平之间的相关性,并评估了对托伐普坦反应的潜在预测因素。

结果

在肝硬化患者的安慰剂组中,相关系数为0.029,在7.5mg托伐普坦组中为-0.112。无论血清白蛋白水平如何,托伐普坦的给药均引发稳定反应。托伐普坦的使用被确定为药理作用的显著预测因素,并且在肝硬化患者中显示可使初始尿量增加885mL(P<0.0001)。

结论

在这项事后分析中,无论血清白蛋白水平如何,托伐普坦均能使基线时的初始尿量增加。对于对袢利尿剂反应不足的患者,将托伐普坦作为袢利尿剂的附加治疗可被视为一种最佳治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ab/4592499/eb7e1965cb89/535_2015_1052_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ab/4592499/2a43ad148295/535_2015_1052_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ab/4592499/d928d9555516/535_2015_1052_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ab/4592499/a7cbf123a7dd/535_2015_1052_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ab/4592499/eb7e1965cb89/535_2015_1052_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ab/4592499/2a43ad148295/535_2015_1052_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ab/4592499/d928d9555516/535_2015_1052_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ab/4592499/a7cbf123a7dd/535_2015_1052_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ab/4592499/eb7e1965cb89/535_2015_1052_Fig4_HTML.jpg

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