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DNA非整倍体与口腔潜在恶性疾病特征的关系:748例细胞学分析

Relationship of DNA aneuploidy with distinctive features of oral potentially malignant disorders: A cytological analysis of 748 cases.

作者信息

Tang Yanyi, Liu Lijun, Li Chenxi, Liu Wei, Shi Linjun

机构信息

Department of General Dentistry, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

College of Stomatology, Shanghai Jiao Tong University, National Center for Stomatology, National Clinical Research Center for Oral Diseases, Shanghai Key Laboratory of Stomatology, Shanghai, China.

出版信息

J Dent Sci. 2022 Apr;17(2):1035-1038. doi: 10.1016/j.jds.2021.10.010. Epub 2021 Oct 26.

Abstract

Our previous study reported that clinical features, including the lateral/ventral tongue and non-homogeneous lesions, were associated with increased risk of malignant changes in cytological samples from oral potentially malignant disorders (OPMDs). This cross-sectional study aimed to evaluate the frequency and risk of DNA aneuploidy in the series of 748 patients with OPMD. The cut-off value of aneuploidy was defined as DNA index ≥3.5. We found that the frequency of DNA aneuploidy was higher in OPMD patients >60 years old, and in those with lateral/ventral tongue sites, non-homogeneous lesions, and high-grade dysplasia, than in control group ( < 0.01). Consistently, the risk of aneuploidy occurrence was higher in patients >60 years old (1.69-fold;  = 0.022), in those with lateral/ventral tongue sites (2.35-fold;  < 0.001), and in those with high-grade dysplasia (3.19-fold;  < 0.001). Collectively, increased frequency and risk of DNA aneuploidy occurred in OPMD patients aged over 60 years with high-grade dysplasia located at the lateral/ventral tongue. These patients should be required to intensive management and follow-up.

摘要

我们之前的研究报告称,临床特征,包括舌外侧/腹侧以及病变不均一性,与口腔潜在恶性病变(OPMD)细胞学样本中恶性变化风险增加相关。这项横断面研究旨在评估748例OPMD患者中DNA非整倍体的频率及风险。非整倍体的临界值定义为DNA指数≥3.5。我们发现,年龄>60岁的OPMD患者、舌外侧/腹侧部位患者、病变不均一性患者以及高级别发育异常患者的DNA非整倍体频率高于对照组(<0.01)。同样,年龄>60岁的患者(1.69倍;=0.022)、舌外侧/腹侧部位患者(2.35倍;<0.001)以及高级别发育异常患者(3.19倍;<0.001)发生非整倍体的风险更高。总体而言,年龄超过60岁、高级别发育异常位于舌外侧/腹侧的OPMD患者中,DNA非整倍体的频率和风险增加。这些患者应接受强化管理和随访。

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