Evidence map›Paper›PMID 40355964›Full record

ArticleBMC research notes2025

The investigation of apoptosis-related genes in periodontitis.

Arezou Sayad, Fatemeh Hashemian, Leila Gholami, Masoud Jamali, Elham Badrlou, Saba Sadeghpour, Naghme Nazer, Sheyda Khalilian, Soudeh Ghafouri-Fard

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Article in BMC research notes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Arezou SayadDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Fatemeh HashemianDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Leila GholamiDepartment of Periodontics, Dental Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Masoud JamaliSarem Hospital, Tehran, Iran.
Elham BadrlouDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Saba SadeghpourDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Naghme NazerDepartment of Electrical Engineering, Sharif University of Technology, Tehran, Iran.
Sheyda KhalilianDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Soudeh Ghafouri-FardDental Research Center, Research Institute for Dental Sciences, Dental School, Shahid Beheshti University of Medical Sciences, Tehran, Iran. s.ghafourifard@sbmu.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study aims at determination of the roles of five apoptosis-related genes, namely CASP2, CASP8, BCL2, HULC and PVT1 in the pathoetiology of periodontitis via measurement of their expressions in both peripheral blood and tissues of affected persons.

resultsCASP2 was over-expressed in gingiva of patients compared with healthy subjects (RME = 24.56, P < 0.001), and in both affected females and males (RME = 30.53, P = 0.03 and RME = 20.59, P = 0.01, respectively). BCL2 was higher in affected tissues compared with controls (RME = 32.28, P < 0.001) and in affected tissues of males versus controls (RME = 69.03, P < 0.001). Finally, HULC had lower level in the blood of patients (RME = 0.21, P = 0.01) and in the blood of female patients compared with normal females (RME = 0.15, P = 0.01). Other comparisons yielded no significant results. BCL2 and CASP2 had the highest diagnostic values for separation of diseased gingival tissues from normal ones. HULC has the best values in the distinction of blood samples of affected persons from control persons. Combination of transcript levels of CASP2, CASP8, BCL2, HULC and PVT1 changed AUC to 0.84 and 0.72 in tissues and blood samples, respectively. To conclude, these genes might be regarded as putative contributors in the pathophysiology of periodontitis.

Indexed as

ApoptosisPeriodontitisAdultCase-Control StudiesCaspase 8FemaleGingivaHumansMaleMiddle AgedProto-Oncogene Proteins c-bcl-2RNA, Long NoncodingBCL2 protein, humanCASP8 protein, humanCaspase 8Proto-Oncogene Proteins c-bcl-2PVT1 long-non-coding RNA, humanRNA, Long NoncodingB-Cell CLL/Lymphoma 2Caspase2Caspase 8HULCPeriodontitisPvt1

Identifiers

PMID40355964
PMCPMC12070626

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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.