Blanton Susan H, Burt Amber, Stal Samuel, Mulliken John B, Garcia Elizabeth, Hecht Jacqueline T
University of Miami, Miller School of Medicine, Miami, FL, USA.
Birth Defects Res A Clin Mol Teratol. 2010 Apr;88(4):256-9. doi: 10.1002/bdra.20659.
Nonsyndromic cleft lip with or without cleft palate is a common birth defect. Although a number of susceptibility loci have been reported, replication has often been lacking. This is likely due, in part, to the heterogeneity of datasets and methodologies. Two independent genome-wide association studies of individuals of largely western European extraction have identified a possible susceptibility locus on 8q24.21.
To determine the overall effect of this locus, we genotyped six of the previously associated single nucleotide polymorphisms in our Hispanic and non-Hispanic white family-based datasets and evaluated them for linkage and association. In addition, we genotyped a large African American family with nonsyndromic cleft lip with or without cleft palate that we had previously mapped to the 8q21.3-24.12 region to test for linkage.
There was no evidence for linkage to this region in any of the three ethnic groups. Nevertheless, strong evidence for association was noted in the non-Hispanic white group, whereas none was detected in the Hispanic dataset.
These results confirm the previously reported association and provide evidence suggesting that there is ethnically based heterogeneity for this locus.
非综合征性唇裂伴或不伴腭裂是一种常见的出生缺陷。尽管已经报道了多个易感基因座,但常常缺乏重复性研究。这可能部分归因于数据集和方法的异质性。两项针对主要为西欧血统个体的独立全基因组关联研究在8q24.21上确定了一个可能的易感基因座。
为了确定该基因座的总体影响,我们在西班牙裔和非西班牙裔白人基于家系的数据集中对先前相关的六个单核苷酸多态性进行了基因分型,并评估它们的连锁和关联情况。此外,我们对一个患有非综合征性唇裂伴或不伴腭裂的大型非裔美国家系进行了基因分型,该家系先前已定位到8q21.3 - 24.12区域以检测连锁情况。
在这三个种族群体中均未发现与该区域存在连锁的证据。然而,在非西班牙裔白人组中发现了强烈的关联证据,而在西班牙裔数据集中未检测到关联。
这些结果证实了先前报道的关联,并提供了证据表明该基因座存在基于种族的异质性。