ID | 69406 |
FullText URL | |
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
|
File Version | publisher
|
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
|
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 )
|