4.5 Article

Microbial profiles of peri-implant mucositis and peri-implantitis: Submucosal microbial dysbiosis correlates with disease severity

期刊

CLINICAL ORAL IMPLANTS RESEARCH
卷 33, 期 2, 页码 172-183

出版社

WILEY
DOI: 10.1111/clr.13880

关键词

dysbiosis; high-throughput nucleotide sequencing; microbiota; mucositis; peri-implantitis

资金

  1. National Natural Science Foundation of China [82170992, 81801024]

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The microbiome distribution in peri-implant mucositis and peri-implantitis sites was found to be similar, with significant differences at the genus and phylum levels. Microbial dysbiosis was significantly associated with an increase in marginal bone loss.
Objective To investigate the microbiome characteristics of peri-implant mucositis (PM) and peri-implantitis (PI), and to analyse the correlation between disease severity and submucosal microbial dysbiosis. Materials and Methods A cross-sectional study design was conducted. Submucosal biofilm samples from 27 PM sites and 37 PI sites from 64 patients were collected and analysed using 16S rRNA gene sequencing (Illumina). Differences in microbiological profiles between PM and PI were evaluated using the alpha-diversity, beta-diversity and linear discriminant analysis effect size (LEfSe) analysis. The relative abundances of the taxa at the phylum and genus levels were compared using the Wilcoxon rank test and logistic regression. The microbial dysbiosis index (MDI) was calculated, and its relationship with clinical measurements (probing depth, bleeding on probing and marginal bone loss, among others) was analysed using Pearson's correlation coefficient. Results The overall microbiome distribution in the PM and PI sites was similar according to alpha- and beta-diversity. Twenty-three taxa at the genus level and two taxa at the phylum level showed significant differences in relative abundance between the two clinical classifications. Five taxa at the genus level were screened out for the MDI calculation after logistic regression. No clinical measurements but marginal bone loss showed a significant positive correlation with microbial dysbiosis. Conclusion The microbiome richness, diversity and distribution were similar in PM and PI sites, including both common periodontal bacteria and novel species. In addition, an increase in marginal bone loss was significantly associated with submucosal microbial dysbiosis.

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