Pitiphat Waranuch, Luangchaichaweng Sarunporn, Pungchanchaikul Patimaporn, Angwaravong Onauma, Chansamak Nusara
Department of Community Dentistry, Khon Kaen University, Khon Kaen, Thailand; Chronic Inflammatory and Systemic Diseases Associated with Oral Health Research Group, Khon Kaen University, Khon Kaen, Thailand.
Eur J Oral Sci. 2014 Aug;122(4):265-70. doi: 10.1111/eos.12136. Epub 2014 Jun 12.
Molar incisor hypomineralization (MIH) is a qualitative developmental enamel defect that affects one to four permanent first molars, with or without involvement of permanent incisors. Its etiology is of systemic origin, but is not well understood. Therefore, we conducted this cross-sectional study to examine pre-, peri-, and postnatal risk factors for MIH among children, 7-8 yr of age, in urban areas of Khon Kaen, Thailand. Molar incisor hypomineralization defects were diagnosed using the European Academy of Pediatric Dentistry criteria. Mothers or primary caregivers were interviewed on maternal medical history and habits during pregnancy, pregnancy and delivery complications, and the child's medical history. Molar incisor hypomineralization defects were observed in 78 (27.7%) of 282 children. Multiple logistic regression analysis showed a statistically significant association between the development of MIH and Cesarean section (adjusted OR = 2.0, 95% CI = 1.1-3.7), complications during vaginal delivery (adjusted OR = 4.5, 95% CI = 1.9-11.0), and severe/chronic illness when under 3 yr of age (adjusted OR = 2.9, 95% CI = 1.6-5.0). There was no association of preterm birth and low birth weight with MIH. The results suggest that Cesarean section, complications during vaginal delivery, and poor health during the first 3 yr of life are independent risk factors for MIH.
磨牙切牙矿化不全(MIH)是一种牙釉质发育质性缺陷,可累及一至四颗恒牙第一磨牙,可伴有或不伴有恒牙切牙受累。其病因源于全身,但目前尚未完全明确。因此,我们开展了这项横断面研究,以调查泰国孔敬市城区7至8岁儿童中MIH的产前、围产期和产后危险因素。采用欧洲儿童牙科学会的标准诊断磨牙切牙矿化不全缺陷。对母亲或主要照料者就孕期母亲的病史和习惯、妊娠及分娩并发症以及孩子的病史进行了访谈。在282名儿童中,有78名(27.7%)观察到磨牙切牙矿化不全缺陷。多因素logistic回归分析显示,MIH的发生与剖宫产(校正比值比=2.0,95%可信区间=1.1 - 3.7)、阴道分娩期间的并发症(校正比值比=4.5,95%可信区间=1.9 - 11.0)以及3岁前的严重/慢性疾病(校正比值比=2.9,95%可信区间=1.6 - 5.0)之间存在统计学显著关联。早产和低出生体重与MIH无关联。结果表明,剖宫产、阴道分娩期间的并发症以及生命最初3年的健康状况不佳是MIH的独立危险因素。