Wang Yin-Ping, Zhang Jie, Zhu Hong-Yi, Qian Chang-Ling, Liu Hua, Ji Fu, Shen Zhi-Yong
Department of General Surgery, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, 1630 Dongfang Road, Shanghai, 200127, People's Republic of China.
Tumour Biol. 2014 May;35(5):4067-75. doi: 10.1007/s13277-013-1532-2. Epub 2013 Dec 28.
Genome-wide association studies have identified 8q24.21-rs6983267 as a new colorectal cancer (CRC) and colorectal adenoma (CRA) susceptibility locus in populations of European descent. Since then, the relationship between 8q24.21-rs6983267 and CRC/CRA has been reported in various ethnic groups; however, these studies have yielded inconsistent results. To investigate this inconsistency and derive a more precise estimation of the relationship, we conducted a meta-analysis of 31 studies, including 51,293 cases and 58,962 controls for CRC, and 8,148 cases and 17,065 controls for CRA. Potential sources of heterogeneity and publication bias were also systematically explored. Overall, the summary odds ratio of G variant for CRC was 1.18 (95% CI, 1.16-1.21; P < 10(-5)) and 1.17 (95% CI, 1.11-1.23; P < 10(-5)) for CRA. Significant results were observed using dominant or recessive genetic model for the polymorphism. In the subgroup analysis by ethnicity, significantly increased risks were found in East Asians and Caucasian populations; while no significant associations were detected among African Americans. After stratifying by sample size and control source, significant associations were also obtained. This meta-analysis suggests that the 8q24.21-rs6983267 polymorphism is associated with CRC/CRA susceptibility, but these associations vary in different ethnic populations.
全基因组关联研究已将8q24.21-rs6983267确定为欧洲血统人群中一个新的结直肠癌(CRC)和结直肠腺瘤(CRA)易感基因座。自那时以来,8q24.21-rs6983267与CRC/CRA之间的关系已在不同种族群体中得到报道;然而,这些研究结果并不一致。为了调查这种不一致性并更精确地估计两者之间的关系,我们对31项研究进行了荟萃分析,其中包括51293例CRC病例和58962例对照,以及8148例CRA病例和17065例对照。我们还系统地探讨了异质性和发表偏倚的潜在来源。总体而言,CRC中G变体的汇总比值比为1.18(95%可信区间,1.16-1.21;P<10^(-5)),CRA为1.17(95%可信区间,1.11-1.23;P<1)0^(-5))。对于该多态性,使用显性或隐性遗传模型观察到显著结果。在按种族进行的亚组分析中,东亚人和白种人群体的风险显著增加;而在非裔美国人中未检测到显著关联。按样本量和对照来源分层后,也获得了显著关联。这项荟萃分析表明,8q24.21-rs6983267多态性与CRC/CRA易感性相关,但这些关联在不同种族人群中有所不同。