PofoliaShared via Pofolia

Journal of Periodontal Research· 2026Q1· Review

Periodontal Medicine Rewired: Mechanisms Linking Periodontitis to Systemic Diseases

Mario Romandini, George Hajishengallis, Mike Curtis, Giacomo Baima

Short summary

Periodontitis triggers systemic disease through seven interconnected mechanisms, including microbial translocation, systemic inflammation, maladaptive myelopoiesis, immune cell trafficking, masticatory dysfunction leading to dietary changes, oral microbiome dysregulation, and shared underlying vulnerabilities like aging and stress.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Periodontitis is linked to over 70 systemic conditions via seven identified mechanistic pathways.
  • Mechanisms include microbial translocation, systemic inflammation, maladaptive myelopoiesis, immune player trafficking, masticatory dysfunction, oral microbiome dysregulation, and shared underlying vulnerabilities.
  • These pathways challenge the traditional direct vs. indirect classification of periodontitis's systemic impact.
  • Shared vulnerabilities such as aging, oxidative stress, and psychosocial stress contribute to both periodontitis and other multi-morbidities.

AI-generated from the title and abstract; the full text is not read.

Abstract

Periodontitis is now recognized not merely as a localized oral condition but as a systemic disease linked to over 70 communicable and non-communicable conditions. This Review explores the key mechanistic pathways-or "gum-shots"-underpinning the systemic impact of periodontitis. Seven interwoven mechanisms are identified. The first, microbial translocation, involves oral pathobionts and virulence factors breaching anatomical barriers and gaining systemic access via hematological, respiratory, and enteral routes, contributing to tissue damage at extra-oral sites. The second, systemic (meta)inflammation, implicates both the spillover of inflammatory mediators from periodontal tissues into circulation and the immune response to translocated pathogens, fueling pro-inflammatory processes. The third, maladaptive myelopoiesis, involves the periodontitis-associated maladaptive trained immunity and aging-related clonal hematopoiesis of indeterminate potential in the bone marrow, leading to myeloid cells with heightened proinflammatory potential. The fourth, immune players trafficking, centers on the systemic repercussions of periodontally generated autoantibodies, translocated orally primed inflammatory cells, and other local immune events. The fifth, masticatory dysfunction-mediated dietary alterations, involves compromised chewing efficiency that alters dietary intake, resulting in nutritional and metabolic imbalances. The sixth, functional dysregulation of the oral microbiome, describes how periodontitis alters the metabolic activity of this densely populated microbial "superorganism", with downstream effects on both oral and systemic physiology. The final mechanism, shared underlying vulnerabilities, refers to background entities-such as biological aging, oxidative stress, psychosocial stress, (epi)genetic predispositions, certain viral infections, and potentially other as-yet-unknown contributors-that drive multi-morbidity, including periodontitis. By dissecting these interconnected pathways, this critical Review challenges the traditional dichotomy of direct versus indirect mechanisms, revealing a more intricate and dynamic interplay.

The authors' abstract, as published at the source. Journal of Periodontal Research, 2026 · DOI ↗

TakeawaysPremium
Ask the paperFree account

Continue with a free account

Ask the paper: 3 free questions a day about this paper; save it, get its citation, new summaries every day for your field. Takeaways are Premium.

Continue free on the web

Sign in with Google or Apple; no card needed. You come back to this paper.

On your phone:

Field: Periodontics

PeriodonticsDentistry