# Periodontitis and Mild Cognitive Impairment Risk in Diabetic Patients: Insights from an Exploratory Analysis

**Authors:** Aulia Ramadhani, Kumiko Minagawa, Sachiko Takehara, Noboru Kaneko, Takaho Yamada, Masaru Kitazawa, Hirohito Sone, Yusran Ady Fitrah, Kaname Nohno, Hiroshi Ogawa

PMC · DOI: 10.3390/dj13110505 · 2025-11-03

## TL;DR

This study explores how periodontitis might increase the risk of mild cognitive impairment in diabetic patients through systemic inflammation.

## Contribution

The study identifies a novel correlation between periodontal inflammation and MCI risk in type II diabetes patients.

## Key findings

- Higher periodontal inflammation (PISA) is linked to increased MCI risk in diabetic patients.
- TTR levels and PISA scores are significantly correlated with MCI risk.
- ApoA1 and C3 show correlations with inflammatory markers CRP and IL-6.

## Abstract

Background: Cognitive impairment, including dementia, is a growing global health challenge, particularly as populations age. Previous studies have identified periodontitis and diabetes mellitus as modifiable risk factors for dementia, potentially linked through systemic inflammation. We hypothesize that systemic inflammation induced by periodontitis may contribute to an increased risk of cognitive impairment. Therefore, this study aims to explore the correlation between periodontal inflammation and the risk of Mild Cognitive Impairment (MCI) in type II diabetes mellitus. Materials and Methods: Baseline data analysis was performed as an analytical cross-sectional study among diabetic patients aged 40 and older who met the inclusion criteria from a randomized controlled trial (RCT) from November 2020 to April 2023. Periodontal inflammation was measured using the Periodontal Inflamed Surface Area (PISA) score. The MCI risk score was calculated using blood samples to assess eight protein markers correlated to MCI (ApoA1, TTR, C3, Albumin, ApoC1, A1BG, A2AP, and HPX). Fisher’s exact test and Spearman’s correlation analysis were performed. Results: 29 T2DM patients were included in the study. There was a significant difference in MCI risk score between the low and high PISA levels group (p < 0.05). Patients with low PISA scores tend to have a lower risk of MCI (p < 0.00). Variables correlated with MCI risk are PISA (ρ = 0.37; p < 0.05) and TTR levels (ρ = −0.51; p < 0.01). ApoA1 has a correlation with CRP (ρ = 0.42; p < 0.05) and IL-6 (ρ = 0.43; p < 0.05), and C3 (ρ = 0.42; p < 0.05) was correlated with CRP. Conclusions: This study found that periodontal inflammation status has a potential correlation to the risk of MCI.

## Linked entities

- **Proteins:** APOA1 (apolipoprotein A1), TTR (transthyretin), C3 (complement C3), LOC100189571 (uncharacterized LOC100189571), APOC1 (apolipoprotein C1), A1BG (alpha-1-B glycoprotein), SERPINF2 (serpin family F member 2), HPX (hemopexin), CRP (C-reactive protein), IL6 (interleukin 6)
- **Diseases:** periodontitis (MONDO:0005076), type II diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Genes:** HPX (hemopexin) [NCBI Gene 3263] {aka HX}, TTR (transthyretin) [NCBI Gene 7276] {aka AMYLD1, ATTR, CTS, CTS1, HEL111, HsT2651}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, SERPINF2 (serpin family F member 2) [NCBI Gene 5345] {aka A2AP, AAP, ALPHA-2-PI, API, PLI, alpha2AP}, APOC1 (apolipoprotein C1) [NCBI Gene 341] {aka APOC1B, Apo-CI, ApoC-I, apo-CIB, apoC-IB}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, A1BG (alpha-1-B glycoprotein) [NCBI Gene 1] {aka A1B, ABG, GAB, HYST2477}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, APOA1 (apolipoprotein A1) [NCBI Gene 335] {aka AMYLD3, HPALP2, apo(a)}
- **Diseases:** dementia (MESH:D003704), MCI (MESH:D060825), type II diabetes mellitus (MESH:D003924), Periodontitis (MESH:D010518), Cognitive Impairment (MESH:D003072), Periodontal inflammation (MESH:D007249), Diabetic (MESH:D003920)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12651057/full.md

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Source: https://tomesphere.com/paper/PMC12651057