Evidence map›Paper›PMID 41390582›Full record

ReviewOdontology2026

Platelet-derived concentrates in the immunological management of periodontitis: from dysbiosis to personalized approaches.

Halil Ata Bıçakçıoğlu, Gülenay Çolak

Abstract readReview
PubMed Publisher
In one paragraph

Review in Odontology, 2026. 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
–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

2 citing papers in PubMed.

  1. Review
  2. 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

2 authors.

Halil Ata BıçakçıoğluDepartment of Periodontology, Faculty of Dentistry, Gazi University, Emek, 06490, Ankara, Turkey. ata.bicakcioglu@icloud.com.ORCID http://orcid.org/0000-0002-2962-0022
Gülenay ÇolakDepartment of Periodontology, Faculty of Dentistry, Gazi University, Emek, 06490, Ankara, Turkey.ORCID http://orcid.org/0000-0002-1171-2228

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Periodontitis is a multifactorial inflammatory disease driven by microbial dysbiosis and host immune dysregulation. Although conventional therapies, such as scaling and root planing or open-flap debridement, focus on biofilm control, they often fail to fully restore immune homeostasis. Consequently, platelet-rich fibrin (PRF) and its derivatives have gained increasing attention as biomaterials with both regenerative and immunomodulatory activity. This review summarizes contemporary insights into the immunopathogenesis of periodontitis, highlighting neutrophil dysfunction, Th17/Treg imbalance, and complement-mediated hyperinflammation as key drivers of tissue destruction. It also synthesizes current evidence on the biological and immunological roles of PRF, including its capacity to promote regulatory T-cell differentiation, modulate macrophage polarization toward an M2 phenotype, and regulate osteoimmunological pathways. Clinical studies show that adjunctive PRF improves probing pocket depth (PPD) reduction, clinical attachment level (CAL) gain, and patient-reported outcomes; however, heterogeneity in preparation protocols and defect characteristics limits comparability across studies. This review uniquely integrates the immunomodulatory mechanisms of platelet-derived concentrates with emerging personalized periodontics, emphasizing how biomarker-based individualization may enhance the predictability of regenerative outcomes.

Indexed as

DysbiosisPeriodontitisPlatelet-Rich FibrinPrecision MedicineHumansImmunomodulationPeriodontitisPlatelet-rich fibrinPrecision medicineTissue engineering

Identifiers

What OpenQuestion 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 OpenQuestion graph.