Repurposing Metformin for periodontal disease management as a form of oral-systemic preventive medicine
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu randomizované kontrolované studie, časopisecké články, práce podpořená grantem
PubMed
37814261
PubMed Central
PMC10563330
DOI
10.1186/s12967-023-04456-1
PII: 10.1186/s12967-023-04456-1
Knihovny.cz E-zdroje
- MeSH
- diabetes mellitus 2. typu * MeSH
- hypoglykemika farmakologie terapeutické užití MeSH
- krevní glukóza MeSH
- lidé MeSH
- management nemoci MeSH
- metformin * farmakologie terapeutické užití MeSH
- nemoci parodontu * farmakoterapie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- hypoglykemika MeSH
- krevní glukóza MeSH
- metformin * MeSH
BACKGROUND: Despite the improvements in treatment over the last decades, periodontal disease (PD) affects millions of people around the world and the only treatment available is based on controlling microbial load. Diabetes is known to increase the risk of PD establishment and progression, and recently, glucose metabolism modulation by pharmaceutical or dietarian means has been emphasised as a significant modulator of non-communicable disease development. METHODS: The impact of pharmaceutically controlling glucose metabolism in non-diabetic animals and humans (REBEC, UTN code: U1111-1276-1942) was investigated by repurposing Metformin, as a mean to manage periodontal disease and its associated systemic risk factors. RESULTS: We found that glucose metabolism control via use of Metformin aimed at PD management resulted in significant prevention of bone loss during induced periodontal disease and age-related bone loss in vivo. Metformin also influenced the bacterial species present in the oral environment and impacted the metabolic epithelial and stromal responses to bacterial dysbiosis at a single cell level. Systemically, Metformin controlled blood glucose levels and age-related weight gain when used long-term. Translationally, our pilot randomized control trial indicated that systemic Metformin was safe to use in non-diabetic patients and affected the periodontal tissues. During the medication window, patients showed stable levels of systemic blood glucose, lower circulating hsCRP and lower insulin levels after periodontal treatment when compared to placebo. Finally, patients treated with Metformin had improved periodontal parameters when compared to placebo treated patients. CONCLUSION: This is the first study to demonstrate that systemic interventions using Metformin in non-diabetic individuals aimed at PD prevention have oral-systemic effects constituting a possible novel form of preventive medicine for oral-systemic disease management.
Centre for Craniofacial and Regenerative Biology FoDOCS King's College London London UK
Institute of Animal Physiology and Genetics Brno Czech Republic
Periodontology Unit Centre for Host Microbiome Interactions FoDOCS King's College London London UK
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