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Replication of GWAS significant loci in a sub-Saharan African Cohort with early childhood caries: a pilot study

机译:在撒哈拉非洲队列中的GWAS重要基点复制幼儿龋:试点研究

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Early childhood caries (ECC) is a rapidly progressing form of dental infection and a significant public health problem, especially among socially and economically disadvantaged populations. This study aimed to assess the risk factors for ECC among a cohort of Sub-Saharan African children and to determine the role of genetics in the etiology of ECC. A sample of 691 children (338 with ECC, 353 without ECC, age??6?years) was recruited from schools in Lagos, Nigeria. Socio-demographic, dental services utilization and infant dietary data were obtained with interviewer-administered questionnaire. Oral examination was conducted using the WHO oral health diagnostic criteria. Saliva samples were collected from the children for genetic analysis. Single nucleotide polymorphisms were selected from previous study for genotyping. Genetic association analyses to investigate the role of genetics in the etiology of ECC was done. Bivariate comparisons and Multivariate logistic regression analyses were conducted to assess associations between ECC and predictor variables, p??0.05. Of the 338 children with ECC, 64 (18.9%) had Severe-Early Childhood Caries (S-ECC). Children aged 48–59?months comprised the highest proportion of subjects with ECC (165; 48.8%) and S-ECC (24; 37.5%) while female subjects had higher dt (3.13?±?2.56) and dmft values 3.27?±?2.64. ECC was significantly more prevalent among children who were breastfed at night?≥?12?months (OR 3.30; CI 0.39, 4.75), those with no previous dental visit (OR 1.71; CI 0.24, 2.77),?those who used sweetened pacifiers (OR 1.85; CI 0.91, 3.79) and those who daily consumed sugar-sweetened drinks/snacks (OR 1.35; CI?0.09, 18.51). A suggestive increased risk for ECC (OR?1.26, p?=?0. 0.0397) was observed for the genetic variant rs11239282 on chromosome 10. We also observed a suggestive reduced risk for ECC (OR?0.80, p?=?0.03) for the rs131777 on chromosome 22. None of the genetic variants were significant after correction for multiple testing (Bonferroni p value p?=?0.004). Prolonged night-time breastfeeding, poor utilization of dental services and daily consumption of sugar were risk factors for ECC. Larger sample size is needed to confirm the results of the genetic analysis and to conduct genome wide studies in order to discover new risk loci for ECC.
机译:儿童早期龋齿(ECC)是一种迅速进展的牙科感染形式,以及具有重要的公共卫生问题,特别是在社会和经济上处于弱势群体中。本研究旨在评估亚撒哈拉非洲儿童队列中ECC的危险因素,并确定遗传学在ECC的病因中的作用。 691名儿童的样本(338名与ECC,353号没有ECC,年龄?使用面试官管理的问卷获得社会人群,牙科服务利用和婴儿饮食数据。使用WHO口腔健康诊断标准进行口头审查。从儿童中收集唾液样品以进行遗传分析。单核苷酸多态性选自以前的基因分型研究。遗传关联分析调查遗传学在ECC的病因中的作用。进行了双变量比较和多变量逻辑回归分析,以评估ECC和预测变量的关联,P≤0.05。在338名患有ECC的儿童中,64名(18.9%)有严重的儿童龋病(S-ECC)。 48-59岁的儿童?月份包括ECC(165; 48.8%)和S-ECC(24; 37.5%)的最高比例,而女性受试者具有较高的DT(3.13?±2.5​​6)和DMFT值3.27?± ?2.64。 ECC在夜间母乳喂养的儿童中显着普遍存在以下?≥?12?月(或3.30; CI 0.39,4.75),没有先前牙科访问的人(或1.71; CI 0.24,2.77),?使用甜味的奶嘴的人(或1.85; CI 0.91,3.79)和每日消耗糖加饮料/小吃的人(或1.35; CI?0.09,18.51)。在染色体上的遗传变异RS11239282观察到ECC(或α1.26,P≤0.0397)的暗示性增加。我们还观察到ECC的暗示性降低(或?0.80,P?= 0.03)对于染色体22的RS131777。校正多种测试后,遗传变异都没有显着(Bonferroni P值P?= 0.004)。长时间夜间母乳喂养,利用贫困性和每日糖的日常消费都是ECC的危险因素。需要更大的样品大小来确认遗传分析的结果并进行基因组的研究,以便发现ECC的新风险基因座。

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