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首页> 外文期刊>Clinical gastroenterology and hepatology: the official clinical practice journal of the American Gastroenterological Association >Placebo in nonalcoholic steatohepatitis: insight into natural history and implications for future clinical trials.
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Placebo in nonalcoholic steatohepatitis: insight into natural history and implications for future clinical trials.

机译:非酒精性脂肪性肝炎的安慰剂:对自然病史的了解以及对未来临床试验的影响。

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BACKGROUND & AIMS: Changes in biochemical and histologic parameters related to nonalcoholic steatohepatitis (NASH) in placebo-treated patients may provide an insight into the natural history and help in defining treatment end points in NASH. The aim of our study was to assess the biochemical and histologic changes seen in the placebo arm of the randomized, placebo-controlled trials in adult patients with NASH. METHODS: Medline was searched (through May 2008) for studies published in the English language. Randomized, placebo-controlled trials of at least 6 months' duration in patients with NASH that provided biochemical and/or histologic data of the placebo arm were included. One investigator performed the literature search and data extraction. Two investigators independently confirmed that the studies met prespecified criteria. Pooled estimates of biochemical and histologic parameters associated with NASH were calculated. RESULTS: Five randomized controlled trials met the predefined criteria and included 162 placebo-treated and 189 active-treatment patients. The mean serum alanine and aspartate aminotransferase levels decreased on placebo. A 1-point improvement in steatosis, ballooning degeneration, lobular inflammation, NASH fibrosis, and combined inflammation scores was seen in 31%, 15%, 33%, 22%, and 32% of patients, respectively. A 2-point improvement in NASH histologic scores is rarely seen. CONCLUSIONS: Serum alanine aminotransferase levels may decrease on placebo and is not a reliable measure of treatment response. Although a 1-point improvement is seen in a third of patients, a 2-point improvement in histologic parameters is rarely seen in the placebo arm and may be more reliable in assessing treatment response. These data may have important implications in designing future clinical trials in NASH.
机译:背景与目的:在安慰剂治疗的患者中,与非酒精性脂肪性肝炎(NASH)相关的生化和组织学参数的变化可能有助于了解自然史,并有助于确定NASH的治疗终点。我们研究的目的是评估在成年NASH患者的随机,安慰剂对照试验的安慰剂组中观察到的生化和组织学变化。方法:搜索Medline(至2008年5月)以英语发表的研究。包括在NASH患者中持续至少6个月的随机安慰剂对照试验,这些试验提供了安慰剂组的生化和/或组织学数据。一名研究人员进行了文献检索和数据提取。两名研究者独立确认研究符合预定标准。计算与NASH相关的生化和组织学参数的汇总估计。结果:五项随机对照试验符合预定标准,包括162名接受安慰剂治疗的患者和189名积极治疗的患者。安慰剂组平均血清丙氨酸和天冬氨酸转氨酶水平下降。分别在31%,15%,33%,22%和32%的患者中观察到脂肪变性,球囊变性,小叶炎症,NASH纤维化和综合炎症评分的1分改善。 NASH组织学评分提高2分的情况很少见。结论:安慰剂可使血清丙氨酸氨基转移酶水平降低,这不是治疗反应的可靠指标。尽管在三分之一的患者中观察到1点改善,但在安慰剂组中很少见到组织学参数改善2点,并且在评估治疗反应时可能更可靠。这些数据可能对设计未来的NASH临床试验具有重要意义。

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