# Periodontal disease and neuroinflammation in multiple sclerosis: a systematic review of current evidence

**Authors:** Srijanani Santhanakrishnan, Karunanidhi Kannappan, Chandrasekaran Krithika, Chitathoor Sridhar, Jaideep Mahendra

PMC · DOI: 10.3389/fdmed.2026.1701357 · Frontiers in Dental Medicine · 2026-02-20

## TL;DR

This review explores the possible link between periodontal disease and multiple sclerosis through shared inflammatory pathways.

## Contribution

The study systematically evaluates the association between periodontal health and MS, highlighting potential clinical correlations.

## Key findings

- MS patients showed poorer periodontal health compared to healthy controls.
- Oral dysbiosis and higher periodontal pathogen abundance were observed in MS patients.
- Elevated oxidative stress and neutrophil-lymphocyte ratios suggest systemic inflammation links.

## Abstract

Multiple Sclerosis (MS) is a chronic, immune-mediated neurological disorder characterized by demyelination and neurodegeneration. Emerging evidence suggests a link between MS and Periodontal Diseases (PD) through shared immune-inflammatory pathways. This review assesses the association between periodontal diseases and multiple sclerosis, focusing on immune-inflammatory interactions and clinical correlations. Despite emerging evidence, the strength of association remains unclear due to methodological heterogeneity.

To review and evaluate the literature on the epidemiological association between PD and MS in adults.

A systematic search was conducted in PubMed, Scopus, and Cochrane. Studies with full text articles that are available in English, without time restrictions, that assessed periodontitis, oral microbiome, and salivary biomarkers in relation to MS were included. Observational studies evaluating clinical, microbiological, or immunological associations were selected. Data extraction covered periodontal parameters, salivary biomarkers, periodontal pathogens and disease severity. The risk of bias was evaluated using Newcastle-Ottawa Scale.

The findings indicated that patients with MS had poorer periodontal health, when compared to healthy controls. Dysbiosis in the oral microbiome was observed, with a higher abundance of periodontal pathogens. Patients with MS exhibited elevated neutrophil-lymphocyte ratios and total oxidative stress, indicating a potential link between systemic inflammation and periodontal dysbiosis. While some studies established positive association between PD and MS, others highlighted the need for further investigation due to inconsistent findings in periodontal parameters between MS patients and controls.

Despite methodological heterogeneity, the available limited evidence indicates the association between periodontitis and MS. This highlights the need for standardized periodontal assessments in research involving MS and suggests that periodontal care may hold potential as an adjunct in management of MS.

## Linked entities

- **Diseases:** Multiple Sclerosis (MONDO:0005301)

## Full-text entities

- **Genes:** HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123] {aka DRB1, HLA-DR1B, HLA-DRB, SS1}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** axon loss (MESH:D012183), neurologic disturbances (MESH:D009461), vitamin D deficiency (MESH:D014808), Sulcus Bleeding (MESH:D006470), autoimmune disease (MESH:D001327), oral diseases (MESH:D009059), neuroinflammation (MESH:D000090862), diabetes (MESH:D003920), Dysbiosis (MESH:D064806), endothelial dysfunction (MESH:D014652), Periodontitis (MESH:D010518), CNS inflammation (MESH:D007249), Neurodegeneration (MESH:D019636), gingival bleeding (MESH:D005884), MS (MESH:D009103), immune dysregulation (OMIM:614878), PD (MESH:D010510), systemic (MESH:D015619), Gingivitis (MESH:D005891), infection (MESH:D007239), chronic periodontitis (MESH:D055113), demyelination (MESH:D003711), gum disease (MESH:C537732)
- **Chemicals:** cortisol (MESH:D006854), vitamin D (MESH:D014807), LPS (MESH:D008070), MDA (MESH:D008315), CP (-)
- **Species:** Meleagris gallopavo (common turkey, species) [taxon 9103], Treponema denticola (species) [taxon 158], gut metagenome (species) [taxon 749906], Homo sapiens (human, species) [taxon 9606], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Porphyromonas gingivalis (species) [taxon 837]

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963300/full.md

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Source: https://tomesphere.com/paper/PMC12963300