Goodman A H, Allen L H, Hernandez G P, Amador A, Arriola L V, Chávez A, Pelto G H
Am J Phys Anthropol. 1987 Jan;72(1):7-19. doi: 10.1002/ajpa.1330720103.
Enamel hypoplasias, deficiencies in enamel thickness resulting from disturbances during the secretory phase of enamel development, are generally believed to result from nonspecific metabolic and nutritional disruptions. However, data are scare on the prevalence and chronological distributions. of hypoplasias in populations experiencing mild to moderate malnutrition. The purpose of this article is to present baseline data on the prevalences and chronological distributions of enamel hypoplasias, by sex and for all deciduous and permanent anterior teeth, in 300 5 to 15-year-old rural Mexican children. Identification of hypoplasias was aided by comparison to a published standard (Federation Dentaire Internationale: Int. Dent. J. 32(2):159-167, 1982). The location of defects, by transverse sixths of tooth crowns, was used to construct distributions of defects by age at development. One or more hypoplasias were detected in 46.7% (95% CI = 40.9-52.5%) of children. Among the unworn and completely erupted teeth, the highest prevalence of defects was found on the permanent maxillary central incisors (44.4% with one or more hypoplasias), followed by the permanent maxillary canine (28.0%) and the remaining permanent teeth (26.2 to 22.2%) Only 6.1% of the completely erupted and unworn deciduous teeth were hypoplastic. The prevalence of enamel defects on the permanent teeth was up to tenfold greater than that found in studies of less marginal populations that used the FDI method. The prevalence of defects in transverse zones suggests a peak frequency of hypoplasias during the second and third years for the permanent teeth, corresponding to the age at weaning in this group. In the deciduous teeth, a smaller peak occurs between 30 and 40 weeks post gestation. The frequency of defects after three years of age is slightly higher in females than males, suggesting a sex difference in access to critical resources.
釉质发育不全是指在釉质发育的分泌阶段受到干扰导致釉质厚度不足,一般认为是由非特异性代谢和营养紊乱引起的。然而,关于经历轻度至中度营养不良人群中釉质发育不全的患病率和时间分布的数据却很稀少。本文的目的是呈现300名5至15岁墨西哥农村儿童中按性别以及所有乳牙和恒牙前牙划分的釉质发育不全的患病率和时间分布的基线数据。通过与已发表的标准(国际牙科联合会:《国际牙科杂志》32(2):159 - 167, 1982)进行比较来辅助识别发育不全。根据牙冠的横向六分之一来确定缺陷位置,以此构建发育时年龄的缺陷分布。46.7%(95%置信区间 = 40.9 - 52.5%)的儿童检测到一个或多个发育不全。在未磨损且完全萌出的牙齿中,缺陷患病率最高的是恒牙上颌中切牙(44.4%有一个或多个发育不全),其次是恒牙上颌尖牙(28.0%)和其余恒牙(26.2%至22.2%)。只有6.1%完全萌出且未磨损的乳牙存在发育不全。恒牙上釉质缺陷的患病率比使用国际牙科联合会方法对边缘性较低人群进行研究时发现的患病率高出多达十倍。横向区域的缺陷患病率表明恒牙在第二和第三年发育不全的频率最高,这与该组儿童断奶的年龄相对应。在乳牙中,较小的峰值出现在妊娠后30至40周之间。三岁以后,女性的缺陷频率略高于男性,这表明在获取关键资源方面存在性别差异。