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Systematic review with meta-analysis: HIF-1 alpha attenuates liver ischemia-reperfusion injury

机译:荟萃分析的系统评价:HIF-1α可减轻肝脏缺血再灌注损伤

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Ischemia-reperfusion injury (IRI) induces inevitable complications in liver transplantation. Many studies have demonstrated that hypoxia-inducible factor 1 alpha (HIF-1 alpha) plays an important role in IRI. However, the mechanism of its pleiotropic effect remains unclear. This systematic review provides a comprehensive evaluation of all available evidence concerning the function of HIF-1 alpha in transplant-induced hepatic IRI. Data were obtained through a search of Medline (PubMed), Embase, and the Cochrane Library literature review on the effect of HIF-1 alpha in IRI (from inception to 12/2014). RevMan was used to calculate standardized mean difference (SMD) and 95% confidence intervals (CIs). Forty articles met inclusion criteria with 2 clinical and 38 basic studies. Two clinical trials (n = 68) revealed ischemic preconditioning (IPC) aroused protection after hepatic IRI based on the higher level of HIF-1 alpha in IPC group compared with control group. In vitro studies confirmed the salutary effect of IPC disappearance in the inhabitation of stabilized HIF-1 alpha. In vivo animal studies showed different HIF-1 alpha expression and distribution patterns in the ischemia and reperfusion stage due to distinctive partial oxygen pressure gradient intra-liver, and 5 animal studies (n = 66) showed that stabilized HIF-1 alpha treatment was associated with lower alanine aminotransferase (ALT) (SMD = 1.58; 95% CI = 2.65, 0.52) when compared with unstabilized HIF-1 alpha group. Not only decreased liver IR injury, stabilized HIF-1 alpha during the acute phase of IR could also promote graft regeneration capacity leading to better initial function and survival rate. More rigorous studies are needed to gauge the effectiveness due to insufficient sample size and possible publication bias. (C) 2015 Elsevier Inc. All rights reserved.
机译:缺血再灌注损伤(IRI)在肝移植中引起不可避免的并发症。许多研究表明,缺氧诱导因子1α(HIF-1 alpha)在IRI中起重要作用。然而,其多效作用的机制仍不清楚。这项系统的综述提供了所有有关移植诱导的肝IRI中HIF-1α功能的现有证据的全面评估。数据是通过检索Medline(PubMed),Embase和Cochrane图书馆文献综述获得的,其中涉及HIF-1α在IRI中的作用(从开始到2014年12月)。 RevMan用于计算标准化均值差(SMD)和95%置信区间(CIs)。符合纳入标准的40篇文章进行了2项临床研究和38项基础研究。两项临床试验(n = 68)显示,由于IPC组中的HIF-1 alpha水平高于对照组,因此缺血性预处理(IPC)在肝IRI后引起了保护。体外研究证实了IPC消失在稳定的HIF-1α居住中的有益作用。体内动物研究显示,由于独特的局部氧气压力梯度肝内传递,在局部缺血和再灌注阶段,HIF-1α表达和分布模式不同,另有5项动物研究(n = 66)表明稳定的HIF-1α治疗与与不稳定的HIF-1α组相比,丙氨酸转氨酶(ALT)较低(SMD = 1.58; 95%CI = 2.65,0.52)。不仅在IR急性期减少了肝脏IR损伤,稳定的HIF-1α还可以促进移植物的再生能力,从而改善初始功能和存活率。由于样本量不足和可能的出版偏倚,需要进行更严格的研究来评估有效性。 (C)2015 Elsevier Inc.保留所有权利。

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