Evidence map›Paper›PMID 26241961›Full record

ArticlePloS one2015

Increased Eotaxin and MCP-1 Levels in Serum from Individuals with Periodontitis and in Human Gingival Fibroblasts Exposed to Pro-Inflammatory Cytokines.

Elisabeth A Boström, Elin Kindstedt, Rima Sulniute, Py Palmqvist, Mirjam Majster, Cecilia Koskinen Holm, Stephanie Zwicker, Reuben Clark, Sebastian Önell, Ingegerd Johansson and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
4.4field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 75 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Serum cytokines in periodontal diseases.Periodontology 2000 · 2025
    Review
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  16. Antibodies toJournal of clinical medicine · 2022
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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

12 authors at 2 institutions in 1 country.

Elisabeth A BoströmKarolinska Institutet, Division of Periodontology, Department of Dental Medicine, Stockholm, Sweden.
Elin KindstedtUmeå University, Department of Molecular Periodontology, Umeå, Sweden.
Rima SulniuteUmeå University, Department of Molecular Periodontology, Umeå, Sweden.
Py PalmqvistUmeå University, Department of Molecular Periodontology, Umeå, Sweden.
Mirjam MajsterKarolinska Institutet, Division of Periodontology, Department of Dental Medicine, Stockholm, Sweden.
Cecilia Koskinen HolmUmeå University, Department of Molecular Periodontology, Umeå, Sweden.
Stephanie ZwickerKarolinska Institutet, Division of Periodontology, Department of Dental Medicine, Stockholm, Sweden.
Reuben ClarkKarolinska Institutet, Division of Periodontology, Department of Dental Medicine, Stockholm, Sweden.
Sebastian ÖnellUmeå University, Department of Molecular Periodontology, Umeå, Sweden.
Ingegerd JohanssonUmeå University, Department of Cariology, Umeå, Sweden.
Ulf H LernerUmeå University, Department of Molecular Periodontology, Umeå, Sweden; University of Gothenburg, Sahlgrenska Academy, Centre for Bone and Arthritis Research, Gothenburg, Sweden.
Pernilla LundbergUmeå University, Department of Molecular Periodontology, Umeå, Sweden.
Umeå University · SEKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Periodontitis is a chronic inflammatory disease of tooth supporting tissues resulting in periodontal tissue destruction, which may ultimately lead to tooth loss. The disease is characterized by continuous leukocyte infiltration, likely mediated by local chemokine production but the pathogenic mechanisms are not fully elucidated. There are no reliable serologic biomarkers for the diagnosis of periodontitis, which is today based solely on the degree of local tissue destruction, and there is no available biological treatment tool. Prompted by the increasing interest in periodontitis and systemic inflammatory mediators we mapped serum cytokine and chemokine levels from periodontitis subjects and healthy controls. We used multivariate partial least squares (PLS) modeling and identified monocyte chemoattractant protein-1 (MCP-1) and eotaxin as clearly associated with periodontitis along with C-reactive protein (CRP), years of smoking and age, whereas the number of remaining teeth was associated with being healthy. Moreover, body mass index correlated significantly with serum MCP-1 and CRP, but not with eotaxin. We detected higher MCP-1 protein levels in inflamed gingival connective tissue compared to healthy but the eotaxin levels were undetectable. Primary human gingival fibroblasts displayed strongly increased expression of MCP-1 and eotaxin mRNA and protein when challenged with tumor necrosis factor-α (TNF-α and interleukin-1β (IL-1β), key mediators of periodontal inflammation. We also demonstrated that the upregulated chemokine expression was dependent on the NF-κΒ pathway. In summary, we identify higher levels of CRP, eotaxin and MCP-1 in serum of periodontitis patients. This, together with our finding that both CRP and MCP-1 correlates with BMI points towards an increased systemic inflammatory load in patients with periodontitis and high BMI. Targeting eotaxin and MCP-1 in periodontitis may result in reduced leukocyte infiltration and inflammation in periodontitis and maybe prevent tooth loss.

Indexed as

AdultAge FactorsBody Mass IndexChemokine CCL11Chemokine CCL2C-Reactive ProteinCytokinesFemaleFibroblastsGingivaHumansInflammationMaleMiddle AgedPeriodontitisPeriodontiumCCL2 protein, humanChemokine CCL11Chemokine CCL2C-Reactive ProteinCytokines

Identifiers

PMID26241961
PMCPMC4524692
OpenAlexW1743721632

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.