Evidence map›Paper›PMID 41947612›Full record

ArticleEuropean journal of oral sciences2026

Alteration in oral and non-oral tissues in ligature-induced periodontitis mice with the Alzheimer's disease risk factor APOE4.

Ae Ri Kim, Yun-Jung Yoo, Eun-Jung Bak

Abstract read
In one paragraph

Article in European journal of oral sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Ae Ri KimDepartment of Oral Biology, Yonsei University College of Dentistry, Seoul, Republic of Korea.ORCID 0000-0002-5661-9596
Yun-Jung YooDepartment of Oral Biology, Yonsei University College of Dentistry, Seoul, Republic of Korea.ORCID 0000-0002-0045-9597
Eun-Jung BakDepartment of Oral Biology, Yonsei University College of Dentistry, Seoul, Republic of Korea.ORCID 0000-0002-7976-8594

Funding

Korea government (MSIT) NRF-2021R1I1A1A01044714National Research Foundation of Korea
6 · The paper itself

Abstract

The APOE4 gene, particularly the ε4 allele, is linked to susceptibility to Alzheimer's disease, and periodontitis can cause pathological changes in multiple organs, but combined effects of these conditions and the impact of tumor necrosis factor (TNF)-α regulation on the combined effects remain unclear. We examined the alterations in oral and non-oral tissues in APOE4-knockin mice with periodontitis and evaluated the effects of infliximab, a TNF-α inhibitor. Mice were grouped as control, periodontitis, APOE4-knockin, APOE4-knockin with periodontitis, infliximab-treated periodontitis, and infliximab-treated APOE4-knockin with periodontitis. There were no differences in alveolar bone volume and periodontal inflammatory cells among all periodontitis-induced groups. The APOE4-knockin with periodontitis group showed a decrease in hippocampal Cornu Ammonis 1 neurons (p < 0.05) and increased renal and hepatic fibrosis (p < 0.05) compared to control group. The infliximab-treated APOE4-knockin with periodontitis group had even greater neuronal loss (p < 0.001) and renal fibrosis (p < 0.01). Glial fibrillary acidic protein mRNA expression, a marker of astrocyte activation, was higher in the infliximab-treated APOE4-knockin with periodontitis group than in the control group. These suggest that APOE4 with periodontitis worsens neuronal loss and renal and hepatic fibrosis, and TNF-α inhibition in this coexistence may have harmful effects on both the brain and kidney.

Indexed as

Alzheimer DiseaseApolipoprotein E4PeriodontitisAnimalsAstrocytesDisease Models, AnimalFibrosisGlial Fibrillary Acidic ProteinHippocampusInfliximabKidneyLiverMaleMiceMice, TransgenicNeuronsApolipoprotein E4Glial Fibrillary Acidic Proteinglial fibrillary astrocytic protein, mouseInfliximabTumor Necrosis Factor-alphainflammationmiceneurodegenerationtransgenictumor necrosis factor‐α

Identifiers

PMID41947612
PMCPMC13377944

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.