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ID 69406
フルテキストURL
suppl1.tiff 9.3 MB
suppl2.tiff 9.3 MB
suppl3.tiff 9.3 MB
著者
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
抄録
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.
キーワード
Continuous glucose monitoring
Periodontal disease
Insulin resistance
Chronic inflammation
Gut flora
発行日
2025-10-06
出版物タイトル
Scientific Reports
15巻
1号
出版者
Springer Science and Business Media LLC
開始ページ
34768
ISSN
2045-2322
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© The Author(s) 2025
論文のバージョン
publisher
PubMed ID
DOI
関連URL
isVersionOf https://doi.org/10.1038/s41598-025-18594-7
ライセンス
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
助成情報
23K27773: 歯周感染・炎症が導く口腔ー子宮連関による新規不妊メカニズムの解明 ( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )
24K22249: 口腔疾患(歯周病)と子宮の連関に着目した新規不妊標的因子の探索 ( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )