Department of Pediatric Dentistry, University of Leipzig, Leipzig, Germany.
LIFE Leipzig Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany.
Int Dent J. 2020 Aug;70(4):303-307. doi: 10.1111/idj.12550. Epub 2020 Feb 11.
The aetiology of deciduous molar hypomineralisation (DMH) is still largely unknown.
The aim of the study was to elucidate the occurrence of DMH as a function of the parameters of bone metabolism, as it is suspected that abnormalities in these parameters may affect the mineralisation of teeth.
In a prospective cohort study, 958 children aged 1-6 years were examined. The inclusion criteria were: a blood sample to determine the parameters of bone metabolism; and documentation of enamel mineralisation using the European Academy of Paediatric Dentistry (EAPD) criteria. Multivariable methods were applied to analyse the incidence of DMH relative to the concentrations of serum calcium, phosphate, vitamin D, vitamin B12 and alkaline phosphatase, taking into account the effects of age, gender and height.
The proportion of children diagnosed with DMH was 4.0% (38 of 958). A significant difference between DMH-affected and non-DMH-affected children was found only in the serum concentration of calcium (2.47 ± 0.08 mmol/l vs. 2.52 ± 0.10 mmol/l, respectively, P = 0.004). The risk of DMH significantly increased, by 1.63-fold (95% CI: 1.03-2.57), if the calcium level dropped by 0.1 mmol/l, regardless of age, gender or adjusted height. During the follow-up examination of 17 DMH-affected subjects, the calcium level remained consistently low 1 year later (t-test, P > 0.05).
Children with DMH showed consistently subclinically lower serum calcium levels. No associations were found for other parameters.
乳磨牙矿化不全(DMH)的病因仍知之甚少。
本研究旨在阐明 DMH 的发生与骨代谢参数的关系,因为怀疑这些参数的异常可能会影响牙齿的矿化。
在一项前瞻性队列研究中,检查了 958 名 1-6 岁的儿童。纳入标准为:采集血样以确定骨代谢参数;并使用欧洲儿童牙科学会(EAPD)标准记录牙釉质矿化情况。应用多变量方法分析血清钙、磷、维生素 D、维生素 B12 和碱性磷酸酶浓度与 DMH 发生率的关系,同时考虑年龄、性别和身高的影响。
被诊断为 DMH 的儿童比例为 4.0%(958 例中的 38 例)。仅在血清钙浓度方面发现 DMH 患儿与非 DMH 患儿之间存在显著差异(分别为 2.47±0.08mmol/l 和 2.52±0.10mmol/l,P=0.004)。如果钙水平下降 0.1mmol/l,DMH 的风险显著增加 1.63 倍(95%CI:1.03-2.57),无论年龄、性别或调整后的身高如何。在 17 名 DMH 患儿的随访检查中,1 年后钙水平仍持续较低(t 检验,P>0.05)。
患有 DMH 的儿童血清钙水平持续偏低,但未发现其他参数与之相关。