E-ISSN 2548-0839
Volume : 10 Issue : 2 Year : 2025

Metrics

1.6
2023 IMPACT FACTOR
2.1
5 year Impact Factor
0.00061
Eigenfactor
3.4
2023 CiteScore
86/157
Journal Citation Reports (Clarivate, 2024)(Dentistry, Oral Surgery & Medicine (Science))
Quartile Q3
SCImago Journal & Country Rank
Expression of Osteogenic Genes in Dental Pulp and Their Correlations in Patients with Clinically Diagnosed Irreversible Pulpitis [Eur Endod J]
Eur Endod J. Ahead of Print: EEJ-24008 | DOI: 10.14744/eej.2025.24008

Expression of Osteogenic Genes in Dental Pulp and Their Correlations in Patients with Clinically Diagnosed Irreversible Pulpitis

Faisal Alonaizan1, Hatem Abuohashish2, J. Francis Borgio3, Sayed Abdul Azeez3, Yaser Alqabbani4, Doaa Al Eraky5
1Department of Restorative Dental Sciences, Imam Abdulrahman Bin Faisal University, College of Dentistry, Dammam, Saudi Arabia
2Department of Biomedical Dental Sciences, Imam Abdulrahman Bin Faisal University, College of Dentistry, Dammam, Saudi Arabia
3Department of Genetic Research, Imam Abdulrahman Bin Faisal University, Institute for Research and Medical Consultations (IRMC), Dammam, Saudi Arabia
4Imam Abdulrahman Bin Faisal University, College of Dentistry, Dammam, Saudi Arabia
5Department of Microbiology and Immunology, Gulf Medical University (GMU), College of Medicine, Ajman, UAE

Objectives: This case-control study aimed to explore the expression of different osteogenic-related genes in inflamed dental pulp and to correlate these expressions amongst each other and with the extent of pain.
Methods: Dental pulp tissues were collected from patients who were diagnosed with irreversible pulpitis. All samples were processed for RNA extraction and analysis of bone morphogenic protein 2 (BMP2), RUNX family transcription factor 2 (RUNX2), dentin sialophosphoprotein (DSPP), dentin matrix acidic phosphoprotein 1 (DMP1), bone gamma-carboxyglutamate protein (BGLAP), and alkaline phosphatase, biomineralization associated (ALPL) gene expression using real-time PCR. Pearson's correlation analysis was used to assess the linear relationships between different genes and the extent of pain.
Results: The demographic and clinical characteristics of the patients varied according to age, sex, tooth type, clinical diagnosis, pain level, percussion pain response, and palpation pain sensitivity. The expression levels of the RUNX2 and BGLAP genes in the inflamed dental pulp were significantly greater than those in the control samples. Pearson's correlation analysis demonstrated significant positive correlations between the expression of the BMP2 and BGLAP genes and between the RUNX2 and DMP1 genes within inflamed pulp tissues.
Conclusion: Irreversible pulpitis was associated with positive coordination among odontoblastic activities, metabolism, and dentin formation as a compensatory mechanism. Our findings provide information on the molecular pathogenesis of pulpitis, suggesting future treatment approaches. (EEJ-2024-11-182)

Keywords: Dental pulp, gene expression, odontogenic, osteogenic, pulpitis

Corresponding Author: Hatem Abuohashish
Manuscript Language: English
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