Zhang W, Qu H C, Zhang Y
Department of Orthodontics, Hospital of Stomatology, China Medical University, Shenyang, Liaoning, China.
Department of Orthodontics, Hospital of Stomatology, China Medical University, Shenyang, Liaoning, China
Genet Mol Res. 2014 Nov 28;13(4):10007-16. doi: 10.4238/2014.November.28.5.
We conducted a comprehensive meta-analysis of 4 case-control studies to explore the association between polymorphisms of Msh homeobox 1 (MSX1) and transforming growth factor-β1 (TGF-β1) genes and hypodontia. A total of 643 tooth agenesis cases and 733 healthy controls were included in this study. The meta-analysis results showed that the T allele and T carrier (CT + TT) of rs1095 in the MSX1 gene were positively associated with hypodontia susceptibility. However, the T allele and T carrier (TC + CC) of rs12532 and rs8670 showed no association with cancer susceptibility. In addition, there were no strong associations between the T allele and T carrier (CT + TT) of C509T and the A allele and A carrier (AG + AA) of G800A in the TGF-β1 gene polymorphisms between patients with tooth agenesis and healthy subjects. In conclusion, these meta-analysis results demonstrated that polymorphisms in the rs1095 region of the MSX1 gene may influence the transcriptional activity of this gene and are associated with hypodontia in humans. However, the association between the TGF-β1 gene and sporadic tooth agenesis is not well understood, and further studies are required to explore the correlation between the TGF-β1 gene and hypodontia.
我们对4项病例对照研究进行了全面的荟萃分析,以探讨Msh同源盒1(MSX1)基因和转化生长因子-β1(TGF-β1)基因多态性与缺牙症之间的关联。本研究共纳入643例牙发育不全病例和733例健康对照。荟萃分析结果显示,MSX1基因中rs1095的T等位基因和T携带者(CT + TT)与缺牙症易感性呈正相关。然而,rs12532和rs8670的T等位基因和T携带者(TC + CC)与癌症易感性无关。此外,在牙发育不全患者和健康受试者之间,TGF-β1基因多态性中C509T的T等位基因和T携带者(CT + TT)以及G800A的A等位基因和A携带者(AG + AA)之间没有强关联。总之,这些荟萃分析结果表明,MSX1基因rs1095区域的多态性可能影响该基因的转录活性,并与人类缺牙症相关。然而,TGF-β1基因与散发性牙发育不全之间的关联尚不清楚,需要进一步研究以探索TGF-β1基因与缺牙症之间的相关性。