Department of Clinical Sciences and Translational Medicine, University of Rome Tor Vergata, via Montpellier 1, 00133, Rome, Italy.
Department of Cardiac Surgery Unit, Centre for Rare Diseases for Marfan Syndrome and Related Disorders, University of Tor Vergata General Hospital, Rome, Italy.
Prog Orthod. 2019 Mar 18;20(1):12. doi: 10.1186/s40510-019-0264-2.
Marfan syndrome is a rare autosomal dominant inherited disease of the connective tissue associated with various craniofacial abnormalities. Aim of the present study was to assess the variability of palatal shape in a sample of 31 Marfan patients compared to a control group of no syndromic subjects, in two stages of dentition, by using 3D geometric morphometric analysis.
Thirty one growing subjects with Marfan syndrome were selected and divided into two subgroups: MG1 with mixed dentition (10 M, 6F, mean age 7+/- 0.7 years), MG2 with permanent dentition (8 M, 7F, mean age 13+/- 0,5 years). Each subgroup was compared to a control group (CG1 mixed dentition, 9 M, 7F, mean age 7.6+/- 0.5 years; CG2 permanent dentition, 9 M, 6F, mean age 12.8+/- 0.7 years) matched on age, sex distribution, stage of dentition and skeletal maturation. Then the two subgroups were compared one to each other. For each patient maxillary dental casts were taken, scanned and digitized. 3D geometric morphometric methods were applied. Procrustes analysis was used and principal component analysis was performed to reveal the main patterns of palatal shape variation.
Both Marfan subgroups showed important reductions in the transversal plane associated with a deep palatal vault when compared to the control groups (MG1 vs CG1 P = 0,003; MG2 vs CG2 P = 0,07). Moreover a statistically significant difference between the palatal shape of MG1 and MG2 was found (P = 0.017) showing a significant worsening of palatal depth and constriction from mixed to permanent dentition in Marfan subjects.
Marfan subjects showed a specific palatal morphology with maxillary constriction and deeper palatal vault when compared to a control group of healthy subjects. The constriction and the depth of the palatal vault in Marfan patients worsen from mixed dentition to permanent dentition more then in no syndromic subjects.
马凡综合征是一种罕见的常染色体显性遗传性结缔组织疾病,与各种颅面异常有关。本研究的目的是通过三维几何形态测量分析,在替牙期和恒牙期两个阶段,比较 31 例马凡综合征患者样本和无综合征对照组的腭部形态差异。
选择 31 名患有马凡综合征的生长中的受试者,并将其分为两个亚组:MG1 混合牙列(10 名男性,6 名女性,平均年龄 7±0.7 岁)和 MG2 恒牙列(8 名男性,7 名女性,平均年龄 13±0.5 岁)。每个亚组均与对照组(CG1 混合牙列,9 名男性,7 名女性,平均年龄 7.6±0.5 岁;CG2 恒牙列,9 名男性,6 名女性,平均年龄 12.8±0.7 岁)进行比较,对照组在年龄、性别分布、牙列阶段和骨骼成熟度方面匹配。然后将两个亚组相互比较。为每位患者取上颌牙列模型,扫描并数字化。应用三维几何形态测量方法。进行 Procrustes 分析和主成分分析,以揭示腭部形态变化的主要模式。
与对照组相比,两个马凡综合征亚组在横向上均表现出重要的减小,伴有腭穹窿变深(MG1 与 CG1 相比,P=0.003;MG2 与 CG2 相比,P=0.07)。此外,还发现 MG1 和 MG2 之间的腭部形状存在统计学显著差异(P=0.017),表明马凡综合征患者从混合牙列到恒牙列时,腭部深度和狭窄程度明显恶化。
与健康对照组相比,马凡综合征患者的腭部形态具有上颌狭窄和腭穹窿变深的特点。与无综合征对照组相比,马凡综合征患者从混合牙列到恒牙列时,腭部狭窄和腭穹窿深度的恶化程度更大。