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From a mouse: systematic analysis reveals limitations of experiments testing interventions in Alzheimer's disease mouse models

机译:从小鼠身上:系统分析揭示了测试对阿尔茨海默氏病小鼠模型进行干预的实验的局限性

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Abstract The increasing prevalence of Alzheimer's disease (AD) poses a considerable socio-economic challenge. Decades of experimental research have not led to the development of effective disease modifying interventions. A deeper understanding of in vivo research might provide insights to inform future in vivo research and clinical trial design. We therefore performed a systematic review and meta-analysis of interventions tested in transgenic mouse models of AD. We searched electronically for publications testing interventions in transgenic models of AD. We extracted data for outcome, study characteristics and reported study quality and calculated summary estimates of efficacy using random effects meta-analysis. We identified 427 publications describing 357 interventions in 55 transgenic models, involving 11,118 animals in 838 experiments. Of concern, reported study quality was relatively low; fewer than one in four publications reported the blinded assessment of outcome or random allocation to group and no study reported a sample size calculation. Additionally, there were few data for any individual intervention?¢????only 16 interventions had outcomes described in 5 or more publications. Finally, ?¢????trim and fill?¢???? analyses suggested one in seven pathological and neurobehavioural experiments remain unpublished. Given these historical weaknesses in the in vivo modelling of AD in transgenic animals and the identified risks of bias, clinical trials that are based on claims of efficacy in animals should only proceed after a detailed critical appraisal of those animal data.
机译:摘要阿尔茨海默氏病(AD)的日益流行给社会经济带来了巨大的挑战。数十年的实验研究尚未导致开发有效的疾病改良干预措施。对体内研究的更深入理解可能会为深入的体内研究和临床试验设计提供见识。因此,我们对在AD转基因小鼠模型中测试的干预措施进行了系统的回顾和荟萃分析。我们以电子方式搜索了测试AD转基因模型干预措施的出版物。我们提取了结果,研究特征的数据,并报告了研究质量,并使用随机效应荟萃分析计算了疗效的汇总估算。我们确定了427个出版物,描述了55个转基因模型中的357种干预措施,涉及838个实验中的11,118只动物。值得关注的是,报道的研究质量相对较低。不到四分之一的出版物报道了对结果的盲法评估或随机分组,并且没有研究报告样本量计算。此外,几乎没有任何单独干预的数据-只有16种干预的结果在5篇或更多出版物中有所描述。最后,?¢ ????修剪并填充?¢ ??????分析表明,尚有七分之一的病理和神经行为实验尚未发表。鉴于转基因动物体内AD建模中的这些历史弱点和确定的偏倚风险,基于动物功效的临床试验仅应在对这些动物数据进行详细的严格评估后才能进行。

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