Evidence map›Paper›PMID 40351293›Full record

ArticleJournal of periodontology2025

Transcriptome analysis of granulation tissue from periodontal osseous defects.

Ye Han Sam, Ana J Caetano, Dewi R Owen, Giuseppe Mainas, Luigi Nibali, Mandeep Ghuman

Abstract read
In one paragraph

Article in Journal of periodontology, 2025. 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
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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

6 authors.

Ye Han SamPeriodontology Unit, Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral and Craniofacial Sciences, King's College London, London, UK.ORCID https://orcid.org/0000-0002-2283-6816
Ana J CaetanoInstitute of Dentistry, Faculty of Medicine and Dentistry, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0003-4588-3241
Dewi R OwenPeriodontology Unit, Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral and Craniofacial Sciences, King's College London, London, UK.ORCID https://orcid.org/0000-0002-2738-1603
Giuseppe MainasPeriodontology Unit, Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral and Craniofacial Sciences, King's College London, London, UK.ORCID https://orcid.org/0000-0002-2778-9756
Luigi NibaliPeriodontology Unit, Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral and Craniofacial Sciences, King's College London, London, UK.ORCID https://orcid.org/0000-0002-7750-5010
Mandeep GhumanPeriodontology Unit, Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral and Craniofacial Sciences, King's College London, London, UK.ORCID https://orcid.org/0000-0001-8927-0741

Funding

Faculty of Dental Oral Craniofacial Sciences, King's College London 20/EE/0241
6 · The paper itself

Abstract

backgroundGranulation tissue is routinely discarded in periodontal surgical procedures, but few studies have characterized it. The present study aimed to compare global gene expression in granulation tissue derived from different types of periodontal osseous defects.

methodsTotal RNA was isolated from granulation tissue harvested during routine periodontal surgical procedures. Nineteen sites were analyzed-seven infrabony, six suprabony, and six furcation defects. Following quality control checks, samples underwent bulk mRNA sequencing (20-30 million read pairs per sample) before bioinformatic analyses utilizing gene ontology and associated pathway/enrichment analyses.

resultsNo statistically significant differentially expressed genes (DEG) were detected between different osseous defect types. An increase in the expression of 11 genes with a false discovery rate of <0.05 was detected when a comparison was made in terms of healing duration post nonsurgical periodontal therapy (NSPT). Notably, the genes involved included those regulating collagen synthesis and osteogenic activity. Analysis based on sex differences revealed 38 DEG. Gene enrichment analysis revealed that 24 DEG without Y-linked attachment are mostly involved in immune regulation.

conclusionsRoutinely discarded periodontal granulation tissue exhibits epithelial characteristics due to a substantial period of maturation post NSPT. Confirmation of ongoing maturation beyond traditional periodontal re-evaluation timepoints warrants further investigation on tissue differentiation potential. More research is needed to elucidate the role of sex as a biological variable affecting periodontal immune response. PLAIN LANGUAGE SUMMARY: Granulation (wound) tissue is routinely removed during gum (periodontal) surgical procedures, but knowledge on its characteristics is scarce. This study aimed to compare gene expression in granulation tissue derived from different types of periodontal bone defects via high-throughput RNA sequencing. Total RNA was extracted from 95 samples harvested from gum disease patients during surgery. After quality control checks, 19 samples (seven infrabony, six suprabony, and six furcation defects) were eligible for sequencing. Subsequent analyses were done utilizing software with known cell biological pathways and processes. Analysis revealed no differentially expressed genes (DEG) in terms of periodontal defect category. There was statistically significantly increased expression of 11 genes when a comparison was made in terms of healing duration following deep scaling treatment. These genes are involved in collagen synthesis and osteogenic activity. Interestingly, analysis based on sex differences detected 38 DEG. Gene enrichment analysis revealed that 24 DEG without association with Y chromosomes are mostly involved in the regulation of immune system response. Routinely discarded periodontal granulation tissue exhibits lining cell characteristics that change over time following deep scaling treatment. More research is needed to unravel the role of sex as a biological variable affecting periodontal immune response in this type of tissue.

Indexed as

Alveolar Bone LossGene Expression ProfilingGranulation TissueTranscriptomeAdultAgedFemaleHumansMaleMiddle Agedgranulation tissueperiodontitisregenerationRNA sequencingwound healing

Identifiers

PMID40351293
PMCPMC12819362

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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.