Suppr超能文献

在中国人群中的复制研究和荟萃分析支持 5p15.33 位点与肺癌的关联。

Replication study in Chinese population and meta-analysis supports association of the 5p15.33 locus with lung cancer.

机构信息

State Key Laboratory of Environment Health (Incubation), Ministry of Education Key Laboratory of Environment & Health, Ministry of Environmental Protection Key Laboratory of Environment and Health, Wuhan, China.

出版信息

PLoS One. 2013 Apr 30;8(4):e62485. doi: 10.1371/journal.pone.0062485. Print 2013.

Abstract

BACKGROUND

Common genetic polymorphisms on chromosome 5p15.33, including rs401681 in cleft lip and palate transmembrane 1-like gene (CLPTM1L), have been implicated in susceptibility to lung cancer through genome-wide association studies (GWAS); however, subsequent replication studies yielded controversial results.

METHODOLOGY AND FINDINGS

A hospital-based case-control study in a Chinese population was conducted to replicate the association, and then a meta-analysis combining our non-overlapping new data and previously published data was performed to clearly discern the real effect of lung cancer susceptibility. In our study with 611 cases and 1062 controls, the minor allele T carrier (TT plus CT) group conferred an OR of 0.801 (95% CI = 0.654-0.981) under the dominant model. The meta-analysis comprising 9111 cases and 11424 controls further confirmed the significant association in the dominant model (OR = 0.842, 95% CI = 0.795-0.891). By stratified analysis, we revealed that ethnicity and study design might constitute the source of between-study heterogeneity. Besides, the sensitivity and cumulative analyses indicated the high stability of the results.

CONCLUSION

The results from our case-control study and meta-analysis provide convincing evidence that rs401681 is significantly associated with lung cancer risk.

摘要

背景

全基因组关联研究(GWAS)表明,5p15.33 染色体上常见的遗传多态性,包括唇裂和腭裂跨膜 1 样基因(CLPTM1L)上的 rs401681,与肺癌易感性有关;然而,随后的复制研究得出了有争议的结果。

方法和发现

在中国人群中进行了一项基于医院的病例对照研究,以复制这种关联,然后进行了一项荟萃分析,将我们非重叠的新数据和以前发表的数据结合起来,以明确区分肺癌易感性的真实影响。在我们的研究中,有 611 例病例和 1062 例对照,在显性模型下,携带次要等位基因 T(TT 加 CT)的个体的比值比(OR)为 0.801(95%可信区间[CI] = 0.654-0.981)。包含 9111 例病例和 11424 例对照的荟萃分析进一步证实了显性模型中的显著关联(OR = 0.842,95%CI = 0.795-0.891)。通过分层分析,我们揭示了种族和研究设计可能是研究间异质性的来源。此外,敏感性和累积分析表明结果具有高度稳定性。

结论

我们的病例对照研究和荟萃分析的结果提供了令人信服的证据,表明 rs401681 与肺癌风险显著相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d22e/3641186/a16557db194c/pone.0062485.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验