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Author
Kubota-Takamori, Moyuka Department of Pathophysiology-Periodontal Science, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Omori, Kazuhiro Department of Pathophysiology-Periodontal Science, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID publons researchmap
Kamei-Nagata, Chiaki Department of Periodontics and Endodontics, Division of Dentistry, Okayama University Hospital
Kiyama, Fumiko Department of Pathophysiology-Periodontal Science, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Ishii, Takayuki Department of Pathophysiology-Periodontal Science, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Nakayama, Masaaki Department of Oral Microbiology, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Gotoh, Kazuyoshi Department of Medical Laboratory Science, Okayama University Graduate School of Health Sciences
Hirai, Kimito Department of Periodontics and Endodontics, Division of Dentistry, Okayama University Hospital
Shinoda-Ito, Yuki Department of Pathophysiology-Periodontal Science, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Okubo, Keisuke Department of Periodontics and Endodontics, Division of Dentistry, Okayama University Hospital
Nakamura, Shin Department of Pathophysiology-Periodontal Science, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Ikeda, Atsushi Department of Periodontics and Endodontics, Division of Dentistry, Okayama University Hospital
Saito, Tsugumichi Department of Health & Sports Sciences, Faculty of Education, Tokyo Gakugei University
Wada, Jun Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID publons researchmap
Takashiba, Shogo Department of Pathophysiology-Periodontal Science, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID publons researchmap
Abstract
Diabetes mellitus (DM) management has advanced from self-monitoring blood glucose (SMBG) to continuous glucose monitoring (CGM), which better prevents complications. However, the influence of periodontitis—a common DM complication—on glucose variability is unclear. This study examined glucose variability in mice with periodontitis using CGM. Periodontitis was induced in 9-week-old male C57BL/6J mice via silk ligatures around the upper second molars. Glucose levels were monitored over 14 days with CGM, validated by SMBG. On day 14, samples were collected to assess alveolar bone resorption and serum levels of tumor necrosis factor-α (TNF-α), insulin, and amyloid A. Glucose tolerance test (GTT) and insulin tolerance test (ITT) were conducted to evaluate insulin resistance. Gut microbiota diversity was also analyzed. By day 10, mice with periodontitis exhibited higher mean glucose levels and time above range than controls. On day 14, serum insulin and amyloid A levels significantly increased, while TNF-α remained unchanged. GTT and ITT indicated insulin resistance. Microbiota analysis showed reduced alpha- and altered beta-diversity, with decreased Coprococcus spp. and increased Prevotella spp., linking dysbiosis to insulin resistance. Periodontitis disrupts glucose regulation by promoting insulin resistance and gut microbiota imbalance, leading to significant glucose variability.
Keywords
Continuous glucose monitoring
Periodontal disease
Insulin resistance
Chronic inflammation
Gut flora
Published Date
2025-10-06
Publication Title
Scientific Reports
Volume
volume15
Issue
issue1
Publisher
Springer Science and Business Media LLC
Start Page
34768
ISSN
2045-2322
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© The Author(s) 2025
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PubMed ID
DOI
Related Url
isVersionOf https://doi.org/10.1038/s41598-025-18594-7
License
http://creativecommons.org/licenses/by-nc-nd/4.0/
Citation
Kubota-Takamori, M., Omori, K., Kamei-Nagata, C. et al. Continuous glucose monitoring reveals periodontitis-induced glucose variability, insulin resistance, and gut microbiota dysbiosis in mice. Sci Rep 15, 34768 (2025). https://doi.org/10.1038/s41598-025-18594-7
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