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RANK RANK / RANKL RANKL / OPG OPG gene polymorphisms and loss of orthodontic mini‐implants

机译:排名等级/ RANKL RANKL / OPG OPG基因多态性和畸形迷你植入物的丧失

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Abstract Objective To investigate the association of genetic polymorphisms ( tag SNPs type) of RANK/RANKL/OPG genes with the loss of orthodontic mini‐implants (MIs). Setting and sample population One hundred and thirty‐five patients of both sexes, with mean age of 48.7?±?10 (20‐76?years), were studied. The control group was composed of 104 patients, with no MI lost and functioning for at least 6?months and the case group, of 31 patients with at least one MI lost. Materials and methods Cells were obtained by mouthwash with 3% glucose solution for 1?minute and scraping the buccal mucosa with sterilized spatula. DNA was extracted from buccal epithelial cells with 10?M ammonium acetate and 1?mM EDTA. Genotyping was performed by the real‐time polymerase chain reaction (PCR) technique. Univariate and multivariate analyses were performed ( P ??.05). Results No markers were associated with MI loss after Benjamini and Hochberg false discovery rate correction of Univariate tests. In the multivariate analysis, the variables that associated with MI loss were the number of MIs installed ( P ??.000) and the polymorphism rs8086340 in the RANK gene ( P ?=?.018). Conclusion A higher number of MIs installed ( P ??.000) and polymorphism rs8086340 in the RANK gene ( P ?=?.018) were associated with loss of orthodontic MIs after multivariate analysis.
机译:摘要目的探讨遗传多态性(标签SNPS型)的遗传多态性(标签SNPS型)与畸形迷你植入物(MIS)的丧失丧失。设定和样本人口百年和三十五名的两性患者,平均年龄为48.7?±10(20-76岁),研究。对照组由104名患者组成,没有MI损失和运作至少6?几个月和案例组,其中31例患者丢失了至少一只MI。材料和方法通过用3%葡萄糖溶液漱口地获得1℃,并用灭菌的刮刀刮擦口腔粘膜。从颊上皮细胞中萃取DNA,其中乙酸钠和1μmEDTA。基因分型由实时聚合酶链反应(PCR)技术进行。进行单变量和多变量分析(p≤≤05)。结果本杰明尼和Hochberg在单变量试验的假冒发现率校正后没有标记与MI损失有关。在多变量分析中,与MI损耗相关的变量是在等级基因中安装的MIS数(P?+。000)和多态性RS8086340(P?= 018)。结论在多变量分析后,在等级基因中安装了更高数量的MIS(P?& 000)和多态性RS8086340和多变量分析后的正畸MIS的损失相关。

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