Montreal Children's Hospital-McGill University, Montreal, Quebec, Canada.
Am J Orthod Dentofacial Orthop. 2013 Mar;143(3):336-41. doi: 10.1016/j.ajodo.2012.10.016.
Osteogenesis imperfecta is a heritable disorder affecting bone and tooth development. Malocclusion is frequent in those affected by osteogenesis imperfecta, but this has not been studied in detail. The purpose of this study was to describe and quantify the severity of malocclusions in patients with osteogenesis imperfecta.
Articulated dental casts were obtained from 49 patients diagnosed with osteogenesis imperfecta (ages 5-19 years; 28 female) and 49 age- and sex-matched control subjects who did not have osteogenesis imperfecta. Both groups were seeking orthodontic treatment. Malocclusions were scored by using the peer assessment rating (PAR) and the discrepancy index (DI).
The average United Kingdom weighted PAR scores were 31.1 (SD, 14.5) for the osteogenesis imperfecta group and 22.7 (SD, 10.7) for the control group (P <0.05). The mean United States weighted PAR scores were 32.2 (SD, 15.0) for patients with osteogenesis imperfecta and 21.6 (SD, 9.6) for the controls (P <0.05). The average modified DI scores were 29.8 (SD, 20.2) for the osteogenesis imperfecta group and 12.4 (SD, 6.8) for the control group (P <0.05). Group differences were greatest for lateral open bite (osteogenesis imperfecta group, 7.1; control group, 0.3) for the DI parameters and anterior crossbite (osteogenesis imperfecta group, 13.0; control group, 3.8 [United Kingdom]) for the PAR.
Both the PAR and the DI showed that malocclusions were significantly more severe in patients with osteogenesis imperfecta than in the control group. There was a higher incidence of Class III malocclusion associated with anterior and lateral open bites in patients affected by osteogenesis imperfecta.
成骨不全症是一种遗传性疾病,影响骨骼和牙齿的发育。错颌畸形在成骨不全症患者中很常见,但尚未对此进行详细研究。本研究旨在描述和量化成骨不全症患者的错颌畸形严重程度。
从 49 名被诊断为成骨不全症(年龄 5-19 岁;28 名女性)的患者和 49 名年龄和性别匹配的无成骨不全症对照组患者中获得可摘戴的牙颌模型。两组患者均寻求正畸治疗。使用同伴评估等级(PAR)和差异指数(DI)对错颌畸形进行评分。
成骨不全症组的平均英国加权 PAR 得分为 31.1(SD,14.5),对照组为 22.7(SD,10.7)(P<0.05)。成骨不全症组患者的平均美国加权 PAR 得分为 32.2(SD,15.0),对照组为 21.6(SD,9.6)(P<0.05)。成骨不全症组的平均改良 DI 得分为 29.8(SD,20.2),对照组为 12.4(SD,6.8)(P<0.05)。在 DI 参数中,侧向开颌(成骨不全症组,7.1;对照组,0.3)和 PAR 中的前牙反颌(成骨不全症组,13.0;对照组,3.8[英国])的组间差异最大。
PAR 和 DI 均表明成骨不全症患者的错颌畸形明显比对照组严重。成骨不全症患者更易发生 III 类错颌畸形,伴前牙和侧向开颌。