Evidence map›Paper›PMID 36902030›Full record

ReviewInternational journal of molecular sciences2023

Molecular Basis beyond Interrelated Bone Resorption/Regeneration in Periodontal Diseases: A Concise Review.

Khadiga M Sadek, Sara El Moshy, Israa Ahmed Radwan, Dina Rady, Marwa M S Abbass, Aiah A El-Rashidy, Christof E Dörfer, Karim M Fawzy El-Sayed

Full text readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 3 pooled it
–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

38 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
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  15. Diabesity and Oral Immunity: Exploring the Interconnection.Advances in experimental medicine and biology · 2026
    Review
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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

8 authors.

Khadiga M SadekBiomaterials Department, Faculty of Dentistry, Cairo University, Cairo 12613, Egypt.ORCID 0000-0002-1466-4743
Sara El MoshyStem Cells and Tissue Engineering Research Group, Faculty of Dentistry, Cairo University, Cairo 12613, Egypt.ORCID 0000-0002-2860-8523
Israa Ahmed RadwanStem Cells and Tissue Engineering Research Group, Faculty of Dentistry, Cairo University, Cairo 12613, Egypt.ORCID 0000-0001-8262-5941
Dina RadyStem Cells and Tissue Engineering Research Group, Faculty of Dentistry, Cairo University, Cairo 12613, Egypt.
Marwa M S AbbassStem Cells and Tissue Engineering Research Group, Faculty of Dentistry, Cairo University, Cairo 12613, Egypt.ORCID 0000-0002-6455-7516
Aiah A El-RashidyBiomaterials Department, Faculty of Dentistry, Cairo University, Cairo 12613, Egypt.ORCID 0000-0002-4475-0837
Christof E DörferClinic for Conservative Dentistry and Periodontology, School of Dental Medicine, Christian Albrechts University, 24118 Kiel, Germany.ORCID 0000-0002-2508-8075
Karim M Fawzy El-SayedStem Cells and Tissue Engineering Research Group, Faculty of Dentistry, Cairo University, Cairo 12613, Egypt.ORCID 0000-0002-6261-3609

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Periodontitis is the sixth most common chronic inflammatory disease, destroying the tissues supporting the teeth. There are three distinct stages in periodontitis: infection, inflammation, and tissue destruction, where each stage has its own characteristics and hence its line of treatment. Illuminating the underlying mechanisms of alveolar bone loss is vital in the treatment of periodontitis to allow for subsequent reconstruction of the periodontium. Bone cells, including osteoclasts, osteoblasts, and bone marrow stromal cells, classically were thought to control bone destruction in periodontitis. Lately, osteocytes were found to assist in inflammation-related bone remodeling besides being able to initiate physiological bone remodeling. Furthermore, mesenchymal stem cells (MSCs) either transplanted or homed exhibit highly immunosuppressive properties, such as preventing monocytes/hematopoietic precursor differentiation and downregulating excessive release of inflammatory cytokines. In the early stages of bone regeneration, an acute inflammatory response is critical for the recruitment of MSCs, controlling their migration, and their differentiation. Later during bone remodeling, the interaction and balance between proinflammatory and anti-inflammatory cytokines could regulate MSC properties, resulting in either bone formation or bone resorption. This narrative review elaborates on the important interactions between inflammatory stimuli during periodontal diseases, bone cells, MSCs, and subsequent bone regeneration or bone resorption. Understanding these concepts will open up new possibilities for promoting bone regeneration and hindering bone loss caused by periodontal diseases.

Indexed as

Alveolar Bone LossPeriodontitisBone RegenerationCytokinesHumansInflammationCytokinesbone regenerationbone resorptioninflammationmesenchymal stem cellosteocytes

Identifiers

PMID36902030
PMCPMC10003253

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read16
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.