Department of Orthodontics, Albaha Dental Centre, Al Bahah, Kingdom of Saudi Arabia.
Department of Orthodontics and Dentofacial Orthopedics, Dr HSRSM Dental College, Hingoli, Maharashtra, India, e-mail:
J Contemp Dent Pract. 2021 Mar 1;22(3):248-252.
This study is conducted to find the association of BMP2 (bone morphogenic protein 2) gene variant rs1005464 and rs15705 with skeletal class I crowding cases.
Blood samples from 60 subjects who visited the Department of Orthodontics and Dentofacial Orthopaedics, D.A.P.M.R.V. Dental College, Bengaluru, were taken after written informed consent. These were divided into two groups: group A with 30 subjects having skeletal class I bases with crowding and group B with 30 subjects having skeletal class I bases without visible crowding or spacing (±2 mm). Around 2 mL of venous blood sample was procured from cases and controls after careful examination. All the samples were then subjected to polymerase chain reaction followed by DNA sequencing and capillary electrophoresis. BMP2 rs1005464 and rs15705 gene variants were assessed and Z-Test was used for statistical analysis.
GG ( = 0.001) and CC ( = 0.0024) genotype of BMP2 gene variant rs1005464 and rs15705, respectively, are significantly associated with skeletal class I crowding cases.
This study concludes that BMP2 variants rs1005464 and rs15705 can be used as genetic markers for skeletal class I bases having crowding.
Predisposing genetic markers BMP2 can be identified prior and this would help in predicting the probability of potential crowding in the future and this would help in early prevention and intervention of crowding.
本研究旨在寻找 BMP2(骨形态发生蛋白 2)基因变体 rs1005464 和 rs15705 与骨骼 I 类拥挤病例的关联。
从 60 名前往班加罗尔 D.A.P.M.R.V.牙科学院正畸和正牙科系就诊的受试者中采集血样,在获得书面知情同意后进行。这些被分为两组:A 组 30 名受试者具有骨骼 I 类基础伴有拥挤,B 组 30 名受试者具有骨骼 I 类基础无明显拥挤或间隙(±2mm)。在仔细检查后,从病例和对照组中采集约 2 毫升静脉血样。所有样本均经过聚合酶链反应、DNA 测序和毛细管电泳。评估 BMP2 rs1005464 和 rs15705 基因变体,并使用 Z 检验进行统计分析。
BMP2 基因变体 rs1005464 的 GG(=0.001)和 rs15705 的 CC(=0.0024)基因型与骨骼 I 类拥挤病例显著相关。
本研究得出结论,BMP2 变体 rs1005464 和 rs15705 可作为具有拥挤的骨骼 I 类基础的遗传标记物。
可以在之前识别出易感性遗传标记物 BMP2,这有助于预测未来潜在拥挤的可能性,并有助于早期预防和干预拥挤。