Vieira A R, Orioli I M, Castilla E E, Cooper M E, Marazita M L, Murray J C
Departments of Pediatrics, 2613 JCP, University of Iowa, Iowa City, 52242-1083, USA.
J Dent Res. 2003 Apr;82(4):289-92. doi: 10.1177/154405910308200409.
MSX1 and TGFB3 have been proposed as genes in which mutations may contribute to non-syndromic forms of oral clefts; however, an interaction between these genes has not been described. The present study attempts to detect transmission distortion of MSX1 and TGFB3 in 217 South American children from their respective mothers. With transmission disequilibrium test analysis, cleft lip with/without cleft palate, cleft lip with palate plus cleft palate only, and all datasets combined showed evidence of association with MSX1 (p = 0.004, p = 0.037, and p = 0.001, respectively). With likelihood ratio test analysis, "cleft lip only" showed association with MSX1 (p = 0.04) and "cleft palate only" with TGFB3 (p = 0.02). A joint analysis of MSX1 and TGFB3 suggested that there may be an interaction between these two loci to increase cleft susceptibility. These results suggest that MSX1 and TGFB3 mutations make a contribution to clefts in South American populations.
MSX1和TGFB3被认为是其突变可能导致非综合征性口腔裂隙的基因;然而,尚未有关于这些基因之间相互作用的描述。本研究试图检测217名南美儿童中MSX1和TGFB3从各自母亲处的传递畸变。通过传递不平衡检验分析,唇裂伴/不伴腭裂、唇裂伴腭裂加单纯腭裂以及所有数据集合并后均显示与MSX1存在关联证据(分别为p = 0.004、p = 0.037和p = 0.001)。通过似然比检验分析,“单纯唇裂”显示与MSX1存在关联(p = 0.04),“单纯腭裂”与TGFB3存在关联(p = 0.02)。MSX1和TGFB3的联合分析表明这两个基因座之间可能存在相互作用以增加裂隙易感性。这些结果表明MSX1和TGFB3突变对南美人群的裂隙形成有影响。