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比较多态性与结直肠癌风险关联研究方法。

A comparison of approaches for association studies of polymorphisms and colorectal cancer risk.

机构信息

Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.

出版信息

Colorectal Dis. 2012 Sep;14(9):e573-86. doi: 10.1111/j.1463-1318.2012.03021.x.

Abstract

AIM

Meta-analyses have been used to evaluate associations between polymorphisms and colorectal cancer risk, but the quality of individual studies used to inform them may vary substantially. Our aim was to apply well-established quality-control criteria to individual association studies and then compare the results of meta-analyses that included or excluded studies that did not meet these criteria.

METHOD

We used meta-analyses of studies reporting a relationship between polymorphisms and colorectal cancer published between 1996 and 2008. Polymorphism-cancer associations were derived in separate meta-analyses including only those meeting the quality-control criteria.

RESULTS

Relative ORs varied substantially between the open and restricted group meta-analyses for all variants except MTHFR 677 CT. However, the associations were modest and the direction of relative risk did not change after applying criteria. Publication bias was detected for all associations, except the restricted set of studies for GSTP1 GG.

CONCLUSION

We observed variation in calculated relative risk and changes in tests for publication bias that were dependent on the inclusion criteria used for association studies of polymorphisms and colorectal cancer. Standardizing study inclusion criteria may reduce the variation in findings for meta-analyses of gene-association studies of common diseases such as colorectal cancer.

摘要

目的

荟萃分析已被用于评估基因多态性与结直肠癌风险之间的关联,但用于提供信息的个别研究的质量可能有很大差异。我们的目的是应用成熟的质量控制标准对个体关联研究进行评估,然后比较包括或排除不符合这些标准的研究的荟萃分析结果。

方法

我们使用了 1996 年至 2008 年期间发表的关于基因多态性与结直肠癌关系的研究的荟萃分析。在分别进行的荟萃分析中,根据质量控制标准仅纳入符合条件的研究,得出了基因多态性与癌症之间的关联。

结果

除 MTHFR 677 CT 外,所有变异体的开放性和受限性荟萃分析中的相对 OR 差异很大。然而,关联程度较小,并且在应用标准后,相对风险的方向并未改变。除 GSTP1 GG 外,所有关联都存在发表偏倚。

结论

我们观察到计算出的相对风险的变化以及对发表偏倚的检验的变化,这取决于用于基因多态性与结直肠癌关联研究的纳入标准。标准化研究纳入标准可能会减少常见疾病(如结直肠癌)的基因关联研究荟萃分析结果的差异。

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