Evidence map›Paper›PMID 40974282›Full record

ArticleJournal of dental research2026

Periodontitis Leads to Systemic Bone Loss through Neutrophil Reprogramming.

K Martin, R Dabaja, M J Mianecki, A Sheikh, V Maglaras, M H A Saleh, J T Decker, A M Decker

Abstract read
In one paragraph

Article in Journal of dental research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Interferon-JAK-STAT Axis in Bone Metabolism.Current osteoporosis reports · 2026
    Review
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

8 authors.

K MartinDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry, Ann Arbor, MI, USA.
R DabajaDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry, Ann Arbor, MI, USA.
M J MianeckiDepartment of Cariology, Restorative Sciences, and Endodontics, University of Michigan School of Dentistry, Ann Arbor, MI, USA.
A SheikhDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry, Ann Arbor, MI, USA.
V MaglarasDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry, Ann Arbor, MI, USA.ORCID 0009-0004-8821-4069
M H A SalehDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry, Ann Arbor, MI, USA.ORCID 0000-0001-5067-7317
J T DeckerDepartment of Cariology, Restorative Sciences, and Endodontics, University of Michigan School of Dentistry, Ann Arbor, MI, USA.ORCID 0000-0001-7914-4741
A M DeckerDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry, Ann Arbor, MI, USA.

Funding

Structure, Composition, & Histology Core - Core BP30AR069620 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KARL J JEPSEN · 2016 to 2026
$8.4M
DSPP Scholar Training at the University of Michigan School of DentistryK12DE027826 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI James Richard Boynton, Yuji MISHINA · 2018 to 2026
$1.4M
Mertk-driven regeneration of alveolar boneR01DE034695 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Ann Marie Decker · 2025 to 2026
$955k
GAS6-mediated alveolar bone regeneration - Admin SupplementR00DE029756 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DECKER, ANN MARIE · 2022 to 2024
$842k
NIAMS NIH HHS P30 AR069620NIDCR NIH HHS K12 DE027826NIDCR NIH HHS R00 DE029756NIDCR NIH HHS R01 DE034695
6 · The paper itself

Abstract

Periodontitis is a chronic oral inflammatory disease characterized by alveolar bone loss. Other diseases, such as osteoporosis, cardiovascular disease, and diabetes, can exacerbate its progression. These chronic diseases also have systemic effects that vary in frequency in men and women. Thus, this study sought to determine if periodontitis induced sex-specific changes in long bones. Periodontitis was induced by tying a 5-0 silk suture around the second maxillary molar of 6- to 8-wk-old male and female C57BL/6J mice. Ligatures were left in place for 7 d or 21 d, and the tibia was subsequently collected for characterization using micro-computed tomography, flow cytometry, and proteomics analysis. Female mice exhibited sustained trabecular and cortical bone loss through day 21, whereas males recovered from any bone loss observed at day 7. Flow cytometry and proteomics analysis indicated that an increased neutrophil response contributes to this bone loss by upregulating pathways associated with neutrophil extracellular trap (NET) formation and reactive oxygen species production. Eliminating NET generation using a Padi4-deficient mouse eliminated the bone loss phenotype during periodontitis. This study suggests that the neutrophil-driven pattern of bone loss observed in female mice, as well as the higher prevalence of osteoporosis in women, may highlight a potential mechanism by which periodontitis exacerbates systemic bone loss.

Indexed as

Alveolar Bone LossNeutrophilsPeriodontitisAnimalsDisease Models, AnimalExtracellular TrapsFemaleFlow CytometryMaleMiceMice, Inbred C57BLProtein-Arginine Deiminase Type 4ProteomicsReactive Oxygen SpeciesSex FactorsTibiapeptidylarginine deiminase 4, mouseProtein-Arginine Deiminase Type 4Reactive Oxygen Speciesbone biologyextracellular trapsgender differencesinflammationneutrophil biologyperiodontal disease

Identifiers

PMID40974282
PMCPMC13044414

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.