Association of MEOX2 polymorphism with nonsyndromic cleft palate only in a Vietnamese population
Association of MEOX2 polymorphism with nonsyndromic cleft palate only in a Vietnamese population
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MEOX2 多态性仅在越南人群中与非综合征性腭裂相关
DOI:
10.1111/cga.12259
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发表时间:
2017
影响因子:
1.3
通讯作者:
Natsume Nagato
中科院分区:
文献类型:
--
作者:
Tran Duy L.;Imura Hideto;Mori Akihiro;Suzuki Satoshi;Niimi Teruyuki;Ono Maya;Sakuma Chisato;Nakahara Shinichi;Nguyen Tham T.H.;Pham Phuong T.;Hoang Viet;Tran Van T.T.;Nguyen Minh D.;Natsume Nagato
To evaluate the association between the single nucleotide polymorphism (SNP) rs227493 in theMEOX2gene and nonsyndromic cleft palate only, this research was conducted as a case–control study by comparing a nonsyndromic cleft palate only group with an independent, healthy, and unaffected control group who were both examined by specialists. Based on clinical examination and medical records, we analyzed a total of 570 DNA samples, including 277 cases and 293 controls, which were extracted from dry blood spot samples collected from both the Odonto and Maxillofacial Hospital in Ho Chi Minh City and Nguyen Dinh Chieu Hospital in Ben Tre province, respectively. The standard procedures of genotyping the specific SNP (rs2237493) forMEOX2were performed on a StepOne Realtime PCR system with TaqMan SNP Genotyping Assays. Significant statistical differences were observed in allelic frequencies (allele T and allele G) between the non‐syndromic cleft palate only and control groups in female subjects, with an allelic odds ratio of 1.455 (95% confidence interval: 1.026–2.064) andP< 0.05. These study findings suggest that nonsyndromic isolated cleft palate might be influenced by variation ofMEOX2, especially SNP rs2237493 in Vietnamese females.