Department of Biostatistics, School of Public Health, Peking University, Beijing, China; Ningbo Municipal Center for Disease Control and Prevention, Ningbo, Zhejiang, China.
Department of Biostatistics, School of Public Health, Peking University, Beijing, China.
Arch Oral Biol. 2022 Apr;136:105384. doi: 10.1016/j.archoralbio.2022.105384. Epub 2022 Feb 18.
To study the association between the seven cell-cell adherens junctions (AJs) -related genes (CDH1, CTNND1, CTNNA1, ESRP1, ESRP2, PLEKHA5, and PLEKHA7) and non-syndromic cleft lip with or without cleft palate (NSCL/P) in the Asian population.
The study included 895 NSCL/P case-parent trios of Asian ethnicity drawn from an international consortium established for a genome-wide association study. We performed association analysis by applying the genotypic transmission disequilibrium test for each of the 144 single nucleotide polymorphisms (SNPs), the versatile gene-based association study for the combined effects of all SNPs, all in or around the seven target genes, and the versatile pathway-based approach for the combined effects of these seven target genes, consecutively.
In our analysis, we found neither a significant SNP-based nor gene-based association with NSCL/P for any of the 144 relevant SNPs or the seven target genes. However, novel evidence of a significant association (P = 6.00 × 10) with NSCL/P was observed in the combined effects of these seven target genes in the versatile pathway-based analysis.
Our results were consistent with the findings of previously published human sequencing studies and reinforced the role of these cell-cell AJs-related genes in the pathogenesis of NSCL/P that may be replicated using data from other genome-wide association studies. This pathway approach better reflects our current understanding of the biological mechanisms underlying the aetiology of NSCL/P.
研究 7 种细胞间黏附连接(AJs)相关基因(CDH1、CTNND1、CTNNA1、ESRP1、ESRP2、PLEKHA5 和 PLEKHA7)与亚洲人群中非综合征性唇裂伴或不伴腭裂(NSCL/P)的关联。
该研究纳入了来自一个国际联盟的 895 个亚洲 NSCL/P 病例-父母三体型,该联盟是为全基因组关联研究而建立的。我们通过对 144 个单核苷酸多态性(SNPs)中的每一个进行基因型传递不平衡检验、对所有 SNPs 的联合效应进行通用基因关联研究、对所有 SNPs 或围绕这 7 个目标基因进行通用途径分析,以及对这 7 个目标基因的联合效应进行通用途径分析,连续应用上述方法进行关联分析。
在我们的分析中,我们没有发现任何与 NSCL/P 相关的 SNP 或基因的显著关联,无论是在 144 个相关 SNPs 中,还是在这 7 个目标基因中。然而,在通用途径分析中,对这 7 个目标基因的联合效应的分析发现了一个与 NSCL/P 有显著关联的新证据(P=6.00×10)。
我们的结果与先前发表的人类测序研究结果一致,强化了这些细胞间 AJs 相关基因在 NSCL/P 发病机制中的作用,使用来自其他全基因组关联研究的数据可以对其进行复制。这种途径方法更好地反映了我们目前对 NSCL/P 病因学的生物学机制的理解。