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European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry · 2025

Cleft lip and palate are associated with a higher prevalence of molar-incisor hypomineralisation: a cross-sectional study with a comparison group.

СтатьяСравнительное исследованиеНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Fonseca-Souza Gabriela, Tessari Vitória, Rolim Tatiane, Gomes-Souza Luíse, Feltrin-Souza Juliana

Аннотация

PURPOSE: To assess the association between non-syndromic cleft lip and/or palate (NSCL/P) and developmental defects of enamel (DDE), including the DDE subtypes, such as molar-incisor hypomineralisation (MIH) and hypomineralised second primary molars (HSPM).

METHODS: This cross-sectional study with a comparison group included individuals with and without NSCL/P ("NSCL/P group" and "control group," respectively). The NSCL/P group was recruited from a specialised craniofacial centre, and the control group was randomly selected from a population-based sample of schoolchildren, in a 1:2 ratio. DDEs were assessed by calibrated examiners through clinical examination. Associations between NSCL/P and DDE were analysed using univariate Poisson regression with robust variance (α = 5%), and comparisons between subtypes included Bonferroni-adjusted p values to account for multiple testing.

RESULTS: The sample included 164 children with NSCL/P and 328 controls (mean age = 8.09 ± 1.39 years). DDEs were more prevalent in the NSCL/P group (76.8%) than in controls (66.2%) (p < 0.01). Hypoplasia, demarcated opacities, and MIH/HSPM were significantly more frequent in the NSCL/P group (p < 0.01). Fluorosis was significantly more prevalent in the control group (p < 0.01). MIH was the most frequent DDE in the NSCL/P group (29.3%). DDEs in the anterior teeth were significantly associated with cleft laterality, being most frequent in bilateral clefts (p < 0.01).

CONCLUSION: Children with NSCL/P have a higher prevalence of DDE than those without clefts. MIH was the most prevalent defect observed in this population, highlighting its clinical relevance.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты