1 Department of Dentistry, Master's Degree Program in Dentistry, Federal University of Sergipe, UFS, Aracaju, Brazil.
2 Department of Dentistry, Discipline of Radiology and Dental Imaging, Federal University of Sergipe, UFS Aracaju, Brazil.
Dentomaxillofac Radiol. 2018 Feb;47(2):20170160. doi: 10.1259/dmfr.20170160. Epub 2017 Nov 13.
To assess cytological evidence of genotoxicity and cytotoxicity of X-rays in oral exfoliated cells of adults subjected to partial and total cone beam CT (CBCT) (stitching module) by means of micronuclei frequency, associated with counting of degenerative nuclear alterations (pyknosis, karyolysis, karyorrhexis, buds and broken eggs), besides comparing the partial and total CBCT (stitching module) in search of possible differences in the nature and/or intensity of the effects.
29 adults who were referred to total or partial CBCT were selected. All CBCT were performed with a Carestream CS 9000 3D scanner (Carestream Health Inc., Rochester, NY). Material collection was done immediately before CBCT and 10 days later, by scraping the left and right cheek mucosa with a plastic spatula. Statistical analysis was performed using the Wilcoxon test (paired data), at a significance level of 5%.
The statistically significant difference was noted in the frequency of micronucleated cells for both partial and total acquisition (p = 0.008 and p < 0.001, respectively). Regarding to cytotoxicity, there was a statistically significant difference for both partial and total acquisition (p < 0.001 and p < 0.001, respectively).
The partial and total CBCT seems to offer risks of inducing genetic damage. In addition both forms of CBCT acquisition have promoted the induction of cytotoxic nuclear alterations.
通过微核频率评估部分和全锥形束 CT(CBCT)(拼接模块)对成人口腔脱落细胞的遗传毒性和细胞毒性,同时对核退行性改变(核固缩、核溶解、核碎裂、芽和破碎卵)进行计数,此外还比较了部分和全 CBCT(拼接模块),以寻找可能存在的效应性质和/或强度差异。
选择了 29 名接受全口或部分 CBCT 的成年人。所有 CBCT 均使用 Carestream CS 9000 3D 扫描仪(Carestream Health Inc.,Rochester,NY)进行。在进行 CBCT 之前和 10 天后,使用塑料刮板刮取左右颊黏膜进行材料采集。使用 Wilcoxon 检验(配对数据)进行统计分析,显著性水平为 5%。
部分和全采集时的微核细胞频率均有统计学显著差异(p=0.008 和 p<0.001)。对于细胞毒性,两种采集方式均有统计学显著差异(p<0.001 和 p<0.001)。
部分和全 CBCT 似乎会带来遗传损伤的风险。此外,两种 CBCT 采集方式都促进了细胞毒性核退行性改变的诱导。