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A Systematic Review of Studies Examining Inflammation Associated Cytokines in Human Abdominal Aortic Aneurysm Samples

机译:系统审查研究人类腹主动脉瘤样本中炎症相关细胞因子的研究

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Objectives: Inflammation is critical in abdominal aortic aneurysm (AAA) but there is no current consensus on which inflammation related cytokines are important. The aim of this review was to systemically assess previous studies investigating the relative expression of inflammation associated cytokines within human AAA samples.Methods: The MEDLINE database was searched for studies which simultaneously examined an array of different inflammation associated cytokines in aortic samples in order to identify those associated with AAA. Focused searches were then conducted for further studies assessing relative concentrations of these cytokines in aortic samples in relation to AAA. Appropriate studies were assessed by two reviewers independently.Results: Eighteen studies were included. A number of different cytokines have been consistently found to be upregulated within AAA by comparison to aortic samples removed from patients without cardiovascular disease, however findings relative to samples of aortic athero-thrombosis were less consistent. TNFA and INFG appear to be the most consistently associated with AAA in studies using both normal and atherosclerotic controls. Cautious interpretation of these data is recommended due to a number of methodological problems.Conclusions: This systematic review suggests that TNFA and INFG are the most consistently upregulated cytokines in large AAAs. Further studies utilizing larger populations, new proteomic techniques and better patient matching are required.
机译:目的:炎症在腹主动脉瘤(AAA)中至关重要,但是目前尚无关于炎症相关细胞因子重要的共识。这篇综述的目的是系统评估以前研究人类AAA样品中炎症相关细胞因子相对表达的研究。方法:搜索MEDLINE数据库以同时检查主动脉样品中一系列不同炎症相关细胞因子的研究,以鉴定与AAA相关的然后进行重点搜索以进行进一步的研究,以评估与AAA相关的主动脉样品中这些细胞因子的相对浓度。适当的研究由两名评价者独立评估。结果:包括18项研究。与没有心血管疾病的患者取出的主动脉样本相比,在AAA中一直发现许多不同的细胞因子被上调,但是相对于主动脉粥样硬化血栓形成样本的发现却不一致。在使用正常和动脉粥样硬化对照的研究中,TNFA和INFG似乎与AAA最一致。由于许多方法上的问题,建议对这些数据进行谨慎的解释。结论:这项系统评价表明,TNFA和INFG是大型AAA中最一致上调的细胞因子。需要使用更大的人群,新的蛋白质组学技术和更好的患者匹配性进行进一步的研究。

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