摘要

目的:本研究分析了3162张CBCT图像,以探索腭中缝(MPS)成熟分期中的年龄和性别特征,并确定MPS骨化的统计学显著年龄阈值。方法:根据Angelieri标准将3162名参与者(1690名女性,1472名男性,年龄3-90岁)的轴向CBCT切片分为六个MPS成熟阶段(A、B、C、D1、D2、E)。Youden指数定义了MPS成熟的诊断年龄阈值;卡方检验评估了年龄、性别与阶段之间的相关性。Kolmogorov-Smirnov检验、t检验和Wilcoxon检验分析了亚组数据分布的相似性,统计显著性设定为p < 0.05。结果:区分MPS阶段A、B、C和D的最佳年龄阈值为11.2岁(男性:11.2岁,女性:10.75岁),具有较高的诊断敏感性和特异性。年龄与MPS成熟显著相关(p < 2.2e-16)。D2阶段在形态上介于D1和E之间但 distinct,其年龄分布与两者均有显著差异(p < 0.05),值得单独分期。青少年(0-20岁)显示出显著的性别差异(p < 0.05),女性成熟较早。结论:关键的MPS骨化年龄阈值为11.2岁,支持减少年轻患者的不必要放射学检查。MPS成熟随年龄进展,且在女性中较早,特别是在0-20岁期间。

原文摘要

OBJECTIVE: This study analyzed 3162 CBCT images to explore age and gender features in midpalatal suture (MPS) maturation staging, and identify the statistically significant age threshold for MPS ossification.

METHODS: Axial CBCT sections of 3162 participants (1690 females, 1472 males, aged 3-90 years) were classified into six MPS maturation stages (A, B, C, D1, D2, E) based on Angelieri's criteria. The Youden index defined the diagnostic age threshold for MPS maturation; chi-squared tests assessed correlations between age, gender and stages. Kolmogorov-Smirnov, t-test and Wilcoxon test analyzed subgroup data distribution similarity, with statistical significance set at p < 0.05.

RESULTS: The optimal age threshold for distinguishing MPS stages A, B, C and D was 11.2 years (males:11.2 years, females:10.75 years), with high diagnostic sensitivity and specificity. Age correlated significantly with MPS maturation (p < 2.2e-16). D2 stage, morphologically intermediate between D1 and E yet distinct, had a significantly different age distribution from both (p < 0.05), warranting independent staging. Adolescents (0-20 years) showed significant gender differences (p < 0.05), with females maturing earlier.

CONCLUSION: The critical MPS ossification age threshold is 11.2 years, supporting reduced unnecessary radiological examinations in younger patients. MPS maturation advances with age and is earlier in females, especially in 0-20 years.

出处

Clinical oral investigations 2026;30(9). DOI: 10.1007/s00784-026-07093-2.

PubMed 原文链接(PMID 42663730)

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