首页> 外文期刊>International journal of paediatric dentistry >Implications of gluten exposure period, CD clinical forms, and HLA typing in the association between celiac disease and dental enamel defects in children. A case-control study.
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Implications of gluten exposure period, CD clinical forms, and HLA typing in the association between celiac disease and dental enamel defects in children. A case-control study.

机译:麸质暴露时间,CD临床形式和HLA分型与儿童乳糜泻和儿童牙釉质缺陷之间的关系。病例对照研究。

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BACKGROUND: The association between coeliac disease (CD) and dental enamel defects (DED) is well known. AIM: The aim of this study was to investigate the prevalence of DED in children with CD and to specifically find the association of DED and gluten exposure period, CD clinical forms, HLA class II haplotype. DESIGN: This study was designed as a matched case-control study: 250 children were enrolled (125 coeliac children - 79 female and 46 male, 7.2 +/- 2.8 years and 125 healthy children). Data about age at CD diagnosis, CD clinical form, and HLA haplotype were recorded. RESULTS: Dental enamel defects were detected in 58 coeliac subjects (46.4%) against seven (5.6%) controls (P < 0.005). We found an association between DED and gluten exposure period, as among CD subjects the mean age at CD diagnosis was significantly (P = 0.0004) higher in the group with DED (3.41 +/- 1.27) than without DED (1.26 +/- 0.7). DED resulted more frequent (100%) in atypical and silent CD forms than in the typical one (30.93%). The presence of HLA DR 52-53 and DQ7antigens significantly increased the risk of DED (P = 0.0017) in coeliac children. CONCLUSIONS: Our results confirmed a possible correlation between HLA antigens and DED.
机译:背景:乳糜泻(CD)与牙釉质缺损(DED)之间的关联是众所周知的。目的:本研究的目的是调查患有CD的儿童中DED的患病率,并特别发现DED与面筋暴露时间,CD临床形式,HLA II类单倍型的关系。设计:该研究被设计为匹配的病例对照研究:招募了250名儿童(125名腹腔儿童-79名女性和46名男性,7.2 +/- 2.8岁和125名健康儿童)。记录有关CD诊断时的年龄,CD临床形式和HLA单倍型的数据。结果:58名腹腔受试者(46.4%)中有7名(5.6%)对照组发现牙釉质缺损(P <0.005)。我们发现DED与面筋暴露时间之间存在关联,因为CD受试者中CD诊断的平均年龄显着(P = 0.0004)在有DED的组(3.41 +/- 1.27)中比没有DED的组(1.26 +/- 0.7)高)。 DED产生的非典型和无声CD形式比典型形式(30.93%)更为频繁(100%)。 HLA DR 52-53和DQ7抗原的存在显着增加了腹腔儿童DED的风险(P = 0.0017)。结论:我们的结果证实了HLA抗原和DED之间可能存在相关性。

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