牙齿上的粉笔状损伤。Molaris Incisivus低矿化的发现历史、预防和再矿化方法的发展

Éva Mlinkó
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引用次数: 0

摘要

磨牙低矿化(MIH)是一种源自外胚层的牙釉质发育障碍。从希波克拉底开始,人们就一直在研究牙齿的结构。Fauchard在1728年首次写了关于硬组织发育障碍的文章。那时他们发现了发育不全对全身性疾病的影响。后来,Busch(1884)和Turner(1909)分别发现恒牙局部发育不良是乳牙炎症的根本原因。1970年,Suckling创建了DDE指数,该指数确定了摩尔低矿化的特征。2001年,MIH一词在EAPD大会上被引入。它的患病率很高,是儿童龋齿的主要危险因素。再矿化对白斑和低矿化牙齿至关重要。1874年,埃尔哈特发现氟化物改变了牙釉质表面,并开始研究氟化物的抗氧作用。系统的氟化实验开始于自来水(1945)、盐(1955)、牛奶和药片。1970年,人们首次认识到局部氟化物摄入也会提高龋齿损伤处的氟化物含量。1977年,费耶斯科夫认识到,高摄入量可能对淀粉性发育有害。其他再矿化方法开始发展,如Schweigert于1946年发现酪蛋白,Reynolds于1987年发现酪蛋白-磷脂,Kleinberg于1979年发现精氨酸,Heinch于2006年发现生物玻璃。需要进一步的实验来开发更有效的预防和/或再矿化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Krétaszerű elváltozások a fogakon. A Molaris Incisivus Hypomineralisatio felfedezésének története, prevenciós és remineralizációs módszerek fejlődése
Molar Incisor Hypomineralisation (MIH) is a developmental disfunction of the enamel of ectodermal origin. Since Hippocrates, the dental structure was studied continously. Fauchard wrote in 1728 first about hard tissue developmental disturbances. At that time they discovered the impact of hypoplasia on systemic diseases. Later Busch in 1884 and Turner in 1909 detected localised hypoplasia on the permanent teeth as the underlying cause of deciduous dental inflammation. 1970 Suckling created the DDE index, which determined the characteristics of molar hypomineralisation. In 2001 the term MIH was introduced at the EAPD congress. Its prevalence is high and it is a primary risk factor of caries in childhood. Remineralisation is crucial at white spots and hypomineralised teeth. In 1874 Erhardt discovered that fluoride changed the enamel surface, and started research to examine its anticariogen effect. Systematic fluoridation experiments where initiated by tap water (1945), salt (1955) milk and pills. It was recognised first in 1970 that topical fluoride intake raised fluoride content in the carious lesions as well. In 1977 Fejerskov recognised that the high intake can be toxic to amelogenesis. Other remineralisation methods started to develop, as casein recognised by Schweigert in 1946, casein-phosphopeptid by Reynolds 1987, arginine by Kleinberg 1979, Bioglass by Heinch 2006. Future experiments are needed to develop more effective prevention and/or remineralisation.
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