Garcete Delvalle Clara Sandibel, De Nova García M Joaquín, Mourelle Martínez María Rosa
Faculty of Dentistry, Complutense University of Madrid, Madrid, Spain.
Calcif Tissue Int. 2025 Feb 7;116(1):37. doi: 10.1007/s00223-025-01345-1.
Osteogenesis imperfecta (OI) is a hereditary disorder characterized by bone fragility and skeletal abnormalities. The administration of bisphosphonates (BPs) in children with OI increases bone density. This antiresorptive inhibits osteoclast action, thus altering physiological processes, in which osteoclasts play important roles, such as the eruptive process. The aim of this investigation was to study the eruptive process (dental development of permanent dentition, resorption of temporary dentition, and alveolar eruption of the first permanent molar) in children with OI medicated with BPs and to compare the results with those of a control group. In total, 34 panoramic radiographs of children with OI [mean chronological age of 8.43 (± 1.77)] who were medicated with BPs for a period of one year or more were studied and 367 panoramic radiographs of healthy children [mean chronological age of 9.19 (± 1.62)] were used as controls. The Demirjian method was used to study the dental development of the seven permanent teeth in the third quadrant. Alveolar eruption of the first permanent molar was considered when perforation of the alveolar bone was produced. The Haavikko method was used to study the root resorption of the five primary teeth in the third quadrant, and software (PixelStick®) was used to measure the lengths of the mesial and distal roots of the primary molars. The cumulative dose of BPs was obtained by mathematically calculating the total dosage received (mg)/weight (kg) and multiplying the relative potency of the medication. The Mann‒Whitney U test was used for comparisons, and p < 0.05 indicated statistical significance. A delay of 0.95 points in dental development and delayed exfoliation of primary dentition between 1.31 and 1.66 years were described in the study group. A root resorption delay of 11.8% was described among the 5 primary teeth of 23.3% among the single-rooted teeth and of 5.6% among the two-rooted teeth in children with OI medicated with BFs (p < 0.05). Delayed alveolar eruption of the first permanent molar at 0.31 years of age was found in children with OI medicated with BFs. We detected delayed tooth development at one stage of maturation in the study group, which was clinically imperceptible. The dental age (≤ 0.55 years) was greater than the chronological age in both groups. We also reported delayed exfoliation of the primary dentition (from 1.31 to 1.66 years), delayed root resorption of the primary dentition (11.8%), and delayed (from 1 mm to 1.25 mm) root resorption of the primary molars in the study group. Although the degree of dental development of the first permanent molar was similar between the two groups, we found delayed (0.31 years) alveolar eruption in the study group and a greater delay (0.44 years) in children whose cumulative dose of bisphosphonates exceeded 2000.
成骨不全症(OI)是一种遗传性疾病,其特征为骨骼脆弱和骨骼异常。给患有OI的儿童使用双膦酸盐(BPs)可增加骨密度。这种抗吸收药物会抑制破骨细胞的作用,从而改变破骨细胞发挥重要作用的生理过程,如萌出过程。本研究的目的是研究接受BPs治疗的OI患儿的萌出过程(恒牙列的牙齿发育、乳牙列的吸收以及第一恒磨牙的牙槽萌出),并将结果与对照组进行比较。总共研究了34例接受BPs治疗一年或更长时间的OI患儿的全景X线片[平均实际年龄为8.43(±1.77)岁],并将367例健康儿童的全景X线片[平均实际年龄为9.19(±1.62)岁]用作对照。采用德米尔坚方法研究第三象限中七颗恒牙的牙齿发育情况。当牙槽骨穿孔时,视为第一恒磨牙的牙槽萌出。采用哈维科方法研究第三象限中五颗乳牙的牙根吸收情况,并使用软件(PixelStick®)测量乳磨牙近中根和远中根的长度。通过数学计算所接受的总剂量(mg)/体重(kg)并乘以药物的相对效力,得出BPs的累积剂量。采用曼-惠特尼U检验进行比较,p<0.05表示具有统计学意义。研究组中描述了牙齿发育延迟0.95分以及乳牙列脱落延迟1.31至1.66年。在接受BFs治疗的OI患儿中,5颗乳牙中有11.8%出现牙根吸收延迟,单根牙中有23.3%出现牙根吸收延迟,双根牙中有5.6%出现牙根吸收延迟(p<0.05)。在接受BFs治疗的OI患儿中,发现第一恒磨牙牙槽萌出延迟0.31岁。我们在研究组中检测到牙齿发育在一个成熟阶段出现延迟,这在临床上不易察觉。两组的牙龄(≤0.55岁)均大于实际年龄。我们还报告了研究组中乳牙列脱落延迟(1.31至1.66年)、乳牙列牙根吸收延迟(11.8%)以及乳磨牙牙根吸收延迟(从1mm至1.25mm)。尽管两组中第一恒磨牙的牙齿发育程度相似,但我们发现研究组中牙槽萌出延迟(0.31岁),并且双膦酸盐累积剂量超过2000的儿童延迟更为明显(0.44岁)。