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声带白斑复发与MDM2 - 309变异在两年内的关联:一项前瞻性研究。

Association of the recurrence of vocal leukoplakia with MDM2-309 variants over a 2-year period: a prospective study.

作者信息

Zhou Jian, Yang Yue, Zhang Duo, Zhou Liang, Liu Fei, Tao Lei, Lu Li-Ming

机构信息

a Department of Otolaryngology , Eye Ear Nose & Throat Hospital, Fudan University , Shanghai , PR China .

b Shanghai Institute of Immunology, Shanghai Jiaotong University School of Medicine , Shanghai , PR China and.

出版信息

Acta Otolaryngol. 2016;136(1):95-9. doi: 10.3109/00016489.2015.1082194. Epub 2015 Sep 15.

Abstract

CONCLUSION

MDM2-309 polymorphism variant genotypes decrease the risk of recurrence in vocal leukoplakia.

OBJECTIVE

The results of a previous study 2 years ago showed the effect of mouse double minute 2 homolog (MDM2) SNP309 polymorphisms in people with laryngeal carcinoma and vocal leukoplakia (a pre-cancerous laryngeal carcinoma lesion). This prospective, clinical trial was performed to assess the relationship between MDM2-309 polymorphism variants and recurrence/cancerization rates in people with vocal leukoplakia over a 2-year period.

PARTICIPANTS AND METHOD

A total of 61 post-operative patients with vocal leukoplakia participated in this prospective, observational, 2-year, follow-up study, and were genotyped for the MDM2-309 gene using pyrosequencing. Recurrence and cancerization rates were used to assess the relationship between the clinical outcome and the genotype variants.

RESULTS

The recurrence rate in the GT genotypes group was lower than that in the normal TT genotype group (17.2% vs 50%, p = 0.05) and there was a significantly lower recurrence rate in the GG genotype group than in the normal TT genotype group (10% vs 50%, p = 0.03). However, there was no statistically significant difference in the cancerization rate between the MDM2-309 variant (GT + GG) genotypes group and the normal TT genotype group (12.2% vs 8.3%, p > 0.05) over the 2-year follow-up period.

摘要

结论

MDM2 - 309基因多态性变异基因型可降低声带白斑的复发风险。

目的

两年前一项研究的结果显示了小鼠双微体2同源物(MDM2)SNP309基因多态性在喉癌和声带白斑(一种喉癌前病变)患者中的作用。本前瞻性临床试验旨在评估MDM2 - 309基因多态性变异与声带白斑患者两年内复发/癌变率之间的关系。

参与者与方法

共有61例声带白斑术后患者参与了这项前瞻性、观察性、为期两年的随访研究,并采用焦磷酸测序法对MDM2 - 309基因进行基因分型。复发率和癌变率用于评估临床结果与基因型变异之间的关系。

结果

GT基因型组的复发率低于正常TT基因型组(17.2%对50%,p = 0.05),GG基因型组的复发率显著低于正常TT基因型组(10%对50%,p = 0.03)。然而在两年的随访期内,MDM2 - 309变异(GT + GG)基因型组与正常TT基因型组之间的癌变率无统计学显著差异(12.2%对8.3%,p>0.05)。

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