Angle Orthod. 2018 Sep;88(5):590-595. doi: 10.2319/101117-687.1. Epub 2018 May 15.
To evaluate the genotoxic and cytotoxic effects of Haas appliances through micronuclei test and cytogenetic damage analysis in buccal mucosa epithelial cells of patients undergoing orthodontic treatment.
Twenty-eight patients, 6-12 years of age and of both genders, who required a Haas appliance for the correction of a posterior crossbite were included. Epithelial cells from the mucosa were collected by gently scraping the inside of both the right and left cheeks. The cells were collected before the insertion of the appliance (T0), 1 month after the device was installed (T1), and again 3 months after the appliance was immobilized (T2). The cells were processed to obtain slides. Feulgen/Fast Green was used as the staining method, and the number of normal, karyolytic, pyknotic, nuclear buds, bi/trinucleated, and micronucleus cells were counted under light microscopy. Cellular abnormalities were evaluated with parametric and nonparametric tests for comparison of the means by analysis of variance testing, Tukey posttest, or the Kruskal-Wallis test and then by Dunn's posttest. The significance level was 5%.
There were no statistically significant changes in the micronuclei in the evaluated periods ( P > .05). Nuclear buds increased at T1 ( P < .05), returning to baseline levels at T2. Other abnormalities (cariolytic, pyknotic, and bi/trinucleated cells) showed a significant increase at T1 and T2 ( P < .0001).
The Haas appliance did not cause an increase in micronuclei in cells of the buccal mucosa. However, statistically significant increases in cariolytic, pyknotic, and bi/trinucleated cells were observed during treatment, suggesting possible DNA damage.
通过颊黏膜上皮细胞微核试验和细胞遗传学损伤分析,评估 Haas 矫治器的遗传毒性和细胞毒性作用。
共纳入 28 名 6-12 岁的患者,他们需要 Haas 矫治器来纠正后牙反颌。通过轻轻刮取双侧脸颊内侧来收集黏膜上皮细胞。在装置插入前(T0)、安装后 1 个月(T1)和装置固定后 3 个月(T2)时采集细胞。处理细胞以获得载玻片。使用 Feulgen/Fast Green 作为染色方法,在光学显微镜下计数正常、核溶解、固缩、核芽、双核/三核和微核细胞的数量。使用方差分析检验、Tukey 后检验或 Kruskal-Wallis 检验和 Dunn 后检验进行参数和非参数检验,比较均值以评估细胞异常。显著性水平为 5%。
在评估期间,微核没有统计学上的显著变化(P>.05)。核芽在 T1 时增加(P<.05),在 T2 时恢复到基线水平。其他异常(核溶解、固缩和双核/三核细胞)在 T1 和 T2 时显著增加(P<.0001)。
Haas 矫治器不会导致颊黏膜细胞微核增加。然而,在治疗过程中观察到核溶解、固缩和双核/三核细胞的统计学显著增加,表明可能存在 DNA 损伤。