4.4 Article

Subgingival microbiota in adult Down syndrome periodontitis

期刊

JOURNAL OF PERIODONTAL RESEARCH
卷 47, 期 4, 页码 500-507

出版社

WILEY
DOI: 10.1111/j.1600-0765.2011.01459.x

关键词

Down syndrome; periodontal; periodontitis; subgingival microbiota

资金

  1. National Institute of Dental and Craniofacial Research, Bethesda, Maryland [R21 DE015012-02]

向作者/读者索取更多资源

Khocht A, Yaskell T, Janal M, Turner BF, Rams TE, Haffajee AD, Socransky SS. Subgingival microbiota in adult Down syndrome periodontitis. J Periodont Res 2012; 47: 500507. (c) 2012 John Wiley & Sons A/S Background and Objective: The subgingival microbiota in Down syndrome and non-Down syndrome adults receiving periodic dental care was examined for 40 bacterial species using checkerboard DNADNA hybridization and the results were related to clinical periodontal attachment loss. Material and Methods: A total of 44 Down syndrome, 66 non-Down syndrome mentally retarded and 83 mentally normal adults were clinically evaluated. This involved, for each subject, the removal of subgingival specimens from three interproximal sites on different teeth; all subgingival samples per subject were then pooled and assessed for the presence and levels of 40 bacterial species using species-specific whole-genomic DNA probes and checkerboard DNADNA hybridization. Significant group differences in species proportions averaged across subjects were evaluated using the KruskalWallis test, and associations between subgingival species and mean subject attachment loss within Down syndrome and non-Down syndrome subject groups were quantified using Pearson correlation and multiple linear regression analysis. Results: Down syndrome subjects exhibited greater attachment loss than non-Down syndrome subjects (p = 0.05). Most microbial species were present in Down syndrome subjects at levels similar to non-Down syndrome subjects, except for higher proportions of Selenomonas noxia, Propionibacterium acnes, Streptococcus gordonii, Streptococcus mitis and Streptococcus oralis in Down syndrome subjects compared with non-Down syndrome study subjects, higher proportions of Treponema socranskii in Down syndrome subjects compared with non-Down syndrome mentally retarded subjects, and higher proportions of Streptococcus constellatus in Down syndrome subjects compared with mentally normal subjects. Down syndrome adults classified with periodontitis revealed higher subgingival levels of T. socranskii than Down syndrome subjects with no periodontitis (p = 0.02). Higher subgingival proportions of S. constellatus, Fusobacterium nucleatum ssp. nucleatum, S. noxia and Prevotella nigrescens showed significant positive correlations (r = 0.350.42) and higher proportions of Actinomyces naeslundii II and Actinomyces odontolyticus showed negative correlations (r = -0.36 to -0.40), with increasing mean subject attachment loss in Down syndrome adults. Conclusion: Individuals with Down syndrome show higher levels of some subgingival bacterial species and specific associations between certain subgingival bacterial species and loss of periodontal attachment. These findings are consistent with the notion that certain subgingival bacteria may contribute to the increased level of periodontal disease seen in Down syndrome individuals and raise the question as to the reason for increased colonization in Down syndrome.

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