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Robust Ligature-Induced Model of Murine Periodontitis for the Evaluation of Oral Neutrophils
Published on: January 21, 2020
Periodontitis Severity and Subgingival Microbiome Variation in Postmenopausal Women: A Stratified Case-Control Study
Irina-Georgeta Sufaru1, Stefan-Lucian Burlea1, Maria-Alexandra Martu1
1Grigore T. Popa University of Medicine and Pharmacy, 700115 Iasi, Romania.
Background:
This study aimed to determine whether osteoporosis is associated with differences in the subgingival microbiome of postmenopausal women, stratified by periodontitis stage.
Methods:
In this observational, stratified case-control study, 166 postmenopausal women were assigned to six strata defined by bone status (osteoporosis vs. normal BMD) and periodontal category (no periodontitis, Stage I-II, Stage III-IV). Standardized pooled subgingival samples were profiled by 16S rRNA gene sequencing. Community structure was evaluated using Bray-Curtis dissimilarity and tested with PERMANOVA (9999 permutations) and prespecified contrasts comparing osteoporosis versus normal BMD within each periodontal category (Holm adjustment). Alpha diversity (Shannon) was assessed using two-way ANOVA.
Results:
Periodontal category was strongly associated with community structure (PERMANOVA R2 = 0.514, pseudo-F = 86.681, p < 0.0001), whereas bone status (R2 = 0.004, p = 0.178) and the bone status × periodontal category interaction (R2 = 0.007, p = 0.294) were not. None of the three prespecified within-category contrasts reached significance after Holm adjustment. Shannon diversity differed by periodontal category (p = 1.93 × 10-24) but not by bone status (p = 0.200), with similar distributions between osteoporosis and normal BMD within each periodontal category.
Conclusions:
In postmenopausal women, periodontitis severity dominates variation in the subgingival microbiome, and osteoporosis does not confer an additional community-level or taxonomic signature when periodontal status is held constant. Longitudinal and multi-omic studies incorporating host-response biomarkers and therapy exposures are warranted to clarify whether osteoporosis influences periodontal susceptibility and progression primarily through host-mediated mechanisms.
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