Evidence map›Paper›PMID 38157091›Full record

ArticleClinical oral investigations2023

Targeted proteomics in a population-based study identifies serum PECAM-1 and TRIM21 as inflammation markers for periodontitis.

Stefan Lars Reckelkamm, Inga Kamińska, Sebastian-Edgar Baumeister, Mariana Ponce-de-Leon, Benjamin Ehmke, Ewa Rodakowska, Joanna Baginska, Michael Nolde, Karol Adam Kamiński

Open access · hybridAbstract read
In one paragraph

Article in Clinical oral investigations, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 35% of its field
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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
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

9 authors at 4 institutions in 3 countries.

Stefan Lars ReckelkammInstitute of Health Services Research in Dentistry, University of Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany. reckelkamm@uni-muenster.de.
Inga KamińskaDepartment of Integrated Dentistry, Medical University of Bialystok, Bialystok, Poland.
Sebastian-Edgar BaumeisterInstitute of Health Services Research in Dentistry, University of Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.
Mariana Ponce-de-LeonChair of Epidemiology at the University Augsburg, University Hospital Augsburg, Augsburg, Germany.
Benjamin EhmkeClinic for Periodontology and Conservative Dentistry, University of Münster, Münster, Germany.
Ewa RodakowskaDepartment of Clinical Dentistry-Cariology Section, University of Bergen, 5020, Bergen, Norway.
Joanna BaginskaDepartment of Dentistry Propaedeutics, Medical University of Bialystok, 15-295, Białystok, Poland.
Michael NoldeInstitute of Health Services Research in Dentistry, University of Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.
Karol Adam KamińskiDepartment of Population Medicine and Lifestyle Diseases Prevention, Medical University of Bialystok, Bialystok, Poland.
University of Münster · DEMedical University of Białystok · PLUniversity Hospital Augsburg · DEUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPeriodontitis (PD) can cause systematic inflammation and is associated with various metabolic processes in the body. However, robust serum markers for these relationships are still lacking. This study aims to identify novel circulating inflammation-related proteins associated with PD using targeted proteomics. MATERIALS AND

methodsWe used population-based, cross-sectional data from 619 participants of the Polish Longitudinal University Study (Bialystok PLUS). Mean pocket probing depth (mPPD) and proportion of bleeding on probing (pBOP) served as exposure variables. Fifty-two inflammation-related proteins were measured using the Olink Target 96 Cardiovascular III and the Olink Target 96 Immune Response panels. Associations between periodontal measures and proteins were tested using covariate-adjusted linear regression models.

resultsAt a false discovery rate of < 0.05, we identified associations of mPPD and pBOP with platelet-endothelial cell adhesion molecule-1 (PECAM-1) and tripartite motif-containing protein 21 (TRIM21).

conclusionThis study revealed novel associations between PD and serum levels of PECAM-1 and TRIM21. Our results suggest that these proteins might be affected by molecular processes that take place in the inflamed periodontium. CLINICAL RELEVANCE: Novel associations of PECAM-1 and TRIM21 with PD indicate promising serum markers for understanding the disease's pathophysiological processes and call for further biomedical investigations.

Indexed as

PeriodontitisProteomicsBiomarkersC-Reactive ProteinCross-Sectional StudiesHumansInflammationPlatelet Endothelial Cell Adhesion Molecule-1BiomarkersC-Reactive ProteinPlatelet Endothelial Cell Adhesion Molecule-1InflammationPeriodontitisProteomicsSerum markers

Identifiers

PMID38157091
PMCPMC10756891
OpenAlexW4390397605

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.