Department of Orthodontics, Faculty of Dental Sciences, SGT University, Gurugram, Haryana, India, Phone: +91 9443455987, e-mail:
Department of Orthodontics, Faculty of Dental Sciences, SGT University, Gurugram, Haryana, India.
J Contemp Dent Pract. 2020 Sep 1;21(9):1008-1011.
To assess correlation among craniofacial proportions and genetic indicators using estrogen receptors (ESR1 and ESR2).
A total of 128 patients undergoing orthodontic treatment with age range 12-18 years of both genders were included. Lateral cephalogram of all subjects were taken. Vertical and sagittal parameters were studied on these cephalogram. Saliva was used for DNA extraction. Real-time polymerase chain reaction was performed for assessment of genetic indicators in ESR1 (rs9340799 and rs2234693) and in ESR2 (rs4986938 and rs1256049).
The mean SN cranial base was 68.4 mm, ANB (sagittal jaw relationship) was 2.8°, Ptm-A maxillary length was 46.2 mm, Go-Pg (mandibular body length) was 68.2 mm, Co-Gn (total mandibular length) was 112.8 mm, lower anterior facial height (ANS-Me) was 58.4 mm, N-Me (total anterior facial height) was 108.4 mm, lower posterior facial height (Co-Go) was 58.7 mm, and S-Go (total posterior facial height) was 72.4 mm. It was found that rs4986938 in ESR2 was linked with S-N dimension, with patients having CC genotype possessing negative correlation values ( value 0.05). Similarly, CC genotype possessed minimum mandibular body dimension, and it was found that rs4986938 in ESR2 was also linked with Go-Pg dimension ( value = 0.02). We found reduction in the ANS-Me values in patients with CC genotype in ESR1 rs2234693 ( value = 0.02), whereas there was no correlation of rest genotype with other craniofacial measurements ( value > 0.05).
Evaluation of ESR1 and ESR2 may show role of genetic markers in disparity of craniofacial dimensions in individuals.
This study provides an outlay and supports the concept of possible correlation between genetic markers and craniofacial measurements.
使用雌激素受体(ESR1 和 ESR2)评估颅面比例和遗传指标之间的相关性。
共纳入 128 名年龄在 12-18 岁之间的接受正畸治疗的男女患者。对所有受试者进行侧颅面摄影。在这些头颅侧位片上研究垂直和矢状参数。使用唾液提取 DNA。进行实时聚合酶链反应以评估 ESR1(rs9340799 和 rs2234693)和 ESR2(rs4986938 和 rs1256049)中的遗传指标。
颅底 SN 的平均值为 68.4mm,ANB(矢状颌关系)为 2.8°,Ptm-A 上颌长度为 46.2mm,Go-Pg(下颌体长)为 68.2mm,Co-Gn(总下颌长度)为 112.8mm,下前面高(ANS-Me)为 58.4mm,N-Me(总前面高)为 108.4mm,下后面高(Co-Go)为 58.7mm,S-Go(总后面高)为 72.4mm。发现 ESR2 中的 rs4986938 与 S-N 维度相关,具有 CC 基因型的患者具有负相关值( 值 0.05)。同样,CC 基因型具有最小的下颌体长,并且发现 ESR2 中的 rs4986938 也与 Go-Pg 维度相关( 值 = 0.02)。我们发现 ESR1 rs2234693 中 CC 基因型患者的 ANS-Me 值降低( 值 = 0.02),而其他基因型与其他颅面测量值没有相关性( 值>0.05)。
ESR1 和 ESR2 的评估可能显示遗传标记在个体颅面尺寸差异中的作用。
本研究提供了一个基础,并支持遗传标记与颅面测量值之间可能存在相关性的概念。