Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.
Hum Mol Genet. 2012 Jan 15;21(2):437-45. doi: 10.1093/hmg/ddr463. Epub 2011 Oct 7.
Central corneal thickness (CCT) is a highly heritable trait. Genes that significantly influence CCT can be candidate genes for common disorders in which CCT has been implicated, such as primary open-angle glaucoma (POAG) and keratoconus. Because the genetic factors controlling CCT in different Asian populations are unclear, we have built on previous work conducted on Singaporean Indians and Malays and extended our hypothesis to individuals of Chinese descent. We have followed up on all suggestive signals of association with CCT (P < 10(-4)) from the previously reported meta-analysis comprising Indians and Malays in a sample of Chinese individuals (n= 2681). In the combined sample (n= 7711), strong evidence of association was observed at four novel loci: IBTK on chromosome 6q14.1; CHSY1 on chromosome 15q26.3; and intergenic regions on chromosomes 7q11.2 and 9p23 (8.01 × 10(-11) < λ(GC) corrected P(meta) < 8.72 × 10(-8)). These four new loci explain an additional 4.3% of the total CCT variance across the sample cohorts over and above that of previously identified loci. We also extend on a previous finding at a fifth locus (AKAP13) where a new single-nucleotide polymorphism (rs1821481, P(meta) = 9.99 × 10(-9)) was found to be significantly more informative compared with the previously reported rs6496932 (P(meta) = 3.64 × 10(-5)). Performing association analysis in Asians may lead to the discovery of ethnic-specific genes that control CCT, offering further mechanistic insights into the regulation of CCT. In addition, it may also provide several candidate genes for interrogation for POAG, keratoconus and possible racial/ethnic variations.
中央角膜厚度(CCT)是一个高度遗传的特征。对 CCT 有显著影响的基因可能是与 CCT 相关的常见疾病的候选基因,例如原发性开角型青光眼(POAG)和圆锥角膜。由于控制不同亚洲人群 CCT 的遗传因素尚不清楚,我们在之前对新加坡印度人和马来人的研究基础上,将我们的假设扩展到中国血统的个体。我们对之前的印度人和马来人元分析报告中与 CCT 有提示意义的关联信号(P<10(-4))进行了随访,该元分析包含了中国个体样本(n=2681)。在合并样本(n=7711)中,在四个新的位点观察到了强烈的关联证据:染色体 6q14.1 上的 IBTK;染色体 15q26.3 上的 CHSY1;以及染色体 7q11.2 和 9p23 上的基因间区域(8.01×10(-11)<λ(GC)校正后的 meta 分析 P 值<8.72×10(-8))。这四个新的位点在样本队列中,除了以前确定的位点外,额外解释了 CCT 总方差的 4.3%。我们还扩展了以前在第五个位点(AKAP13)的发现,在该位点发现了一个新的单核苷酸多态性(rs1821481,meta 分析 P 值=9.99×10(-9)),与之前报道的 rs6496932(meta 分析 P 值=3.64×10(-5))相比,该多态性更具信息性。在亚洲人群中进行关联分析可能会发现控制 CCT 的种族特异性基因,为 CCT 调节提供进一步的机制见解。此外,它还可能为原发性开角型青光眼、圆锥角膜和可能的种族/民族差异提供几个候选基因进行研究。