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A systematic review evaluating the methodological aspects of meta-analyses of genetic association studies in cancer research.

机译:对癌症研究中遗传关联研究的荟萃分析的方法学方面进行系统评价。

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摘要

Meta-analyses and Individual Patient Data (IPD) meta-analyses of genetic association studies are a powerful tool to summarize the scientific evidences, however their application present considerable potential and several pitfalls. We reviewed systematically all published meta-analyses and IPD meta-analyses of genetic association studies in the field of cancer research, searching for relevant studies on the Medline, Embase, and HuGE Reviews Archive databases until January 2009. The association between selected predictors of methodological quality and the year of publication was also evaluated. 144 meta-analyses involving 299 gene-disease associations, and 25 IPD meta-analyses on 83 gene-disease were included. Overall quality of the reports showed a substantial improvement over time, as authors have become more inclusive of primary papers published in all languages since 2005 (P-value = 0.087), as well as statistical heterogeneity and publication bias were evaluated more systematically. Only 35.4% of the meta-analyses, however, adopted a comprehensive bibliographic search strategy to identify the primary reports, 63.9% did not specify the language of the included studies, 39.8% did not test for Hardy-Weinberg Equilibrium (HWE), while 62.2 and 75.9% of the meta-analyses and IPD meta-analyses, respectively, did not declare the scientific rationale for the genetic model chosen. Additionally, the HWE assessment showed a substantial decreasing trend over time (P-value = 0.031) while publication bias was more often evaluated when statistical heterogeneity was actually present (P-value = 0.007). Although we showed a general methodological improvement over time, guidelines on conducting and reporting meta-analyses of genetic association studies are needed to enhance their methodological quality.
机译:遗传关联研究的荟萃分析和患者个人数据(IPD)荟萃分析是总结科学证据的有力工具,但是它们的应用具有巨大的潜力和一些陷阱。我们系统地审查了癌症研究领域中有关遗传关联研究的所有已发表的荟萃分析和IPD荟萃分析,在Medline,Embase和HuGE Reviews存档数据库中寻找相关研究,直至2009年1月。方法学的选定预测因子之间的关联质量和出版年份也进行了评估。包括涉及299个基因疾病关联的144个荟萃分析,以及对83个基因疾病的25个IPD荟萃分析。自2005年以来,报告的总体质量显示出随着时间的推移显着改善,因为从2005年以来,作者已经越来越多地使用所有语言发表了主要论文(P值= 0.087),并且对统计异质性和发表偏见进行了更加系统的评估。但是,只有35.4%的荟萃分析采用了全面的书目检索策略来确定主要报告,63.9%的研究未指定所研究语言,39.8%的研究未进行Hardy-Weinberg平衡(HWE)测试,而分别有62.2%和75.9%的荟萃分析和IPD荟萃分析未阐明所选遗传模型的科学依据。此外,HWE评估显示随着时间的推移出现显着下降的趋势(P值= 0.031),而当实际存在统计异质性时(P值= 0.007),发布偏倚的评估更为频繁。尽管随着时间的推移,我们显示了总体方法的改进,但仍需要进行和报告遗传关联研究的荟萃分析的指南,以提高其方法学质量。

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