# Effects of aging on host responses in gingival crevicular fluid in natural gingivitis

**Authors:** Yung-Ting Hsu, Jonathan Y. An, Johnny Hudson, Diane Daubert, Richard P. Darveau

PMC · DOI: 10.3389/fimmu.2026.1761707 · Frontiers in Immunology · 2026-02-26

## TL;DR

The study found that older people with natural gingivitis have stronger inflammation and less tissue repair compared to younger people.

## Contribution

This study identifies age-related differences in inflammatory and tissue remodeling responses in natural gingivitis.

## Key findings

- Elder patients showed higher levels of MPO, IL-1β, IL-6, and IL-8 compared to younger patients.
- Younger patients exhibited a higher MMP-9/TIMP-1 ratio, indicating more robust tissue turnover.
- Aged periodontium showed greater disease susceptibility and diminished healing capacity.

## Abstract

This study compared host responses against natural gingivitis in the gingival crevicular fluid (GCF) in young and aged periodontium.

This cross-sectional study recruited two patient populations with natural gingivitis in young (18–35 years old) and elder cohorts (36–75 years old). GCF samples were analyzed for 39 inflammatory and tissue remodeling mediators using bead-based multiplex immunoassays. Independent t-tests with false discovery rate adjustments were used to compare mediator expressions between groups.

Forty patients were enrolled in these comparisons, including young patients (n=22) and elder patients (n=18). In comparison with the young group, the elder group had greater clinical attachment loss and higher expression of MPO (p<0.001), IL-1β (p<0.05), IL-6 (p<0.05), and IL-8 (p<0.05). Despite the ratio of MMP-8/TIMP-1 being not significantly different (p>0.05), the young group had greater ratio of MMP-9/TIMP-1 than old group (p<0.01).

The current findings reveal that the inflammatory profiles of young and elder cohorts with natural gingivitis are distinct. The young cohort with natural gingivitis demonstrated lower disease susceptibility and more robust tissue turnover, whereas the aged periodontium was characterized by higher susceptibility to disease and diminished healing capacity.

## Linked entities

- **Proteins:** MPO (myeloperoxidase), IL1B (interleukin 1 beta), IL6 (interleukin 6), CXCL8 (C-X-C motif chemokine ligand 8), MMP8 (matrix metallopeptidase 8), TIMP1 (TIMP metallopeptidase inhibitor 1), MMP9 (matrix metallopeptidase 9)
- **Diseases:** gingivitis (MONDO:0002508)

## Full-text entities

- **Genes:** MMP8 (matrix metallopeptidase 8) [NCBI Gene 4317] {aka CLG1, HNC, MMP-8, PMNL-CL}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, MPO (myeloperoxidase) [NCBI Gene 4353], TIMP1 (TIMP metallopeptidase inhibitor 1) [NCBI Gene 7076] {aka CLGI, EPA, EPO, HCI, TIMP, TIMP-1}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}
- **Diseases:** gingivitis (MESH:D005891), attachment loss (MESH:D017622), inflammatory (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12979528/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12979528/full.md

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Source: https://tomesphere.com/paper/PMC12979528