组织学和超微结构特征对低矿化釉质的化学和机械特性的影响以及临床后果。

Monographs in oral science Pub Date : 2024-01-01 Epub Date: 2024-07-01 DOI:10.1159/000538865
Juliana de Lima Gonçalves, Fabrício Kitazono de Carvalho, Alexandra Mussolino de Queiroz, Francisco Wanderley Garcia de Paula-Silva
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引用次数: 0

摘要

磨牙切牙低矿化(MIH)是釉质缺陷的一种定性类型,是由于釉质有机基质在釉质形成过程中的生物矿化过程失败而导致的。受MIH影响的牙釉质在化学、结构和机械性能方面都会发生变化,从而导致不同的临床反应。MIH翳的颜色从不透光的白色到黄色/棕色不等,这些病变的元素分析显示钙和磷酸盐含量较低,而这些矿物质在健全的牙釉质中含量较高。此外,釉质中还加入了其他分子,如碳酸盐,这种成分具有更高的溶解度,因此低矿化釉质更容易发生后天性断裂。在结构层面上,羟基磷灰石晶体层似乎是无序的,形态发生了变化,这意味着结构中的孔隙度增加。结构孔隙率的增加可能与牙科过敏症有关,而牙科过敏症是 MIH 患者常见的临床反应。在机械性能方面,硬度和弹性模量会降低,这也会使釉质变得更加脆弱。生物矿化不足的原因可能是釉母细胞的功能发生变化,也可能是细胞间连接失效导致蛋白酶(如 MMP-20 和 KLK4)的活性降低。釉质有机基质中蛋白质的增加会影响羟基磷灰石晶体中矿物质的生长和结合,从而使釉质矿化度降低,有机物含量增加,从而影响其特性。MIH患者珐琅质中的这些变化有助于解释这种情况造成的临床影响。
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Implications of Histological and Ultrastructural Characteristics on the Chemical and Mechanical Properties of Hypomineralised Enamel and Clinical Consequences.

Molar incisor hypomineralisation (MIH) is a qualitative type of enamel defect, which occurs due to a failure in the biomineralisation process of the enamel organic matrix during amelogenesis. The tooth enamel affected by MIH shows changes in its chemical, structural, and mechanical properties, leading to different clinical repercussions. The color of MIH opacities varies from opaque white to yellow/brown, and elemental analyses of these lesions show a lower calcium and phosphate content, minerals that are more abundant in sound enamel. Furthermore, the incorporation of other molecules occurs, such as carbonate, a component that provides a greater degree of solubility, thus making hypomineralised enamel more susceptible to posteruptive fractures. At a structural level, the layer of hydroxyapatite crystals appears to be disorganized, with morphological changes, implying a greater degree of porosity in the structure. The increase in porosity of the structure may be associated with dental hypersensitivity, a common clinical repercussion among patients with MIH. Among the mechanical properties, a decrease in hardness and modulus of elasticity occurs, and this also makes the enamel more fragile. Deficiency in biomineralisation can be caused by changes in the function of ameloblasts or by failures at the intercellular junction that result in lower activity of proteases such as MMP-20 and KLK4. The increase in proteins in the organic matrix of enamel impairs the growth and incorporation of minerals into the hydroxyapatite crystals, so that the enamel becomes hypomineralised and has larger organic content, thus having an impact on its properties. These changes present in the enamel with MIH help to explain the clinical repercussions caused by this condition.

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Challenges of Using Scoring Systems for the Assessment of Molar Incisor Hypomineralisation. Clinical Characteristics and Differential Diagnosis of Hypomineralised Second Primary Molars and Molar Incisor Hypomineralisation. Cost-Effectiveness of Managing MIH Teeth. Deciduous Teeth Hypomineralisation and Perinatal Risk Factors. Developmental Defects of Enamel.
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