Evidence map›Paper›PMID 39699986›Full record

ArticleDental press journal of orthodontics2024

Genetic association between Class II division 1 and division 2 malocclusions with PAX9 (rs8004560) gene polymorphism in a tertiary care hospital.

Monika Shukla, Munish Reddy, Kritanjali Singh, Ruchi Saini, Pradeep Raghav, Kaynat Nasser, Nupur Sharma, Aastha Kamrani, Shehla Rafique, Tanjula Shair

Abstract read
In one paragraph

Article in Dental press journal of orthodontics, 2024. 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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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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. 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

10 authors.

Monika ShuklaSubharti Dental College, Department of Orthodontics and Dentofacial Orthopedics (Uttar Pradesh, India).ORCID http://orcid.org/0009-0005-2348-2123
Munish ReddySubharti Dental College, Department of Orthodontics and Dentofacial Orthopedics (Uttar Pradesh, India).ORCID http://orcid.org/0000-0002-3000-2571
Kritanjali SinghSubharti Medical College & Hospital, Central Research and Incubation Center (Uttar Pradesh, India).ORCID http://orcid.org/0000-0002-0533-8428
Ruchi SainiSubharti Dental College, Department of Orthodontics and Dentofacial Orthopedics (Uttar Pradesh, India).ORCID http://orcid.org/0000-0003-4035-8317
Pradeep RaghavSubharti Dental College, Department of Orthodontics and Dentofacial Orthopedics (Uttar Pradesh, India).ORCID http://orcid.org/0000-0001-8267-1120
Kaynat NasserSubharti Medical College, Department of Community Medicine (Uttar Pradesh, India).ORCID http://orcid.org/0000-0002-4105-5062
Nupur SharmaSubharti Dental College, Department of Orthodontics and Dentofacial Orthopedics (Uttar Pradesh, India).ORCID http://orcid.org/0009-0003-3348-0944
Aastha KamraniSubharti Dental College, Department of Orthodontics and Dentofacial Orthopedics (Uttar Pradesh, India).ORCID http://orcid.org/0009-0004-2019-9026
Shehla RafiqueSubharti Dental College, Department of Orthodontics and Dentofacial Orthopedics (Uttar Pradesh, India).ORCID http://orcid.org/0009-0005-7673-8524
Tanjula ShairSubharti Dental College, Department of Orthodontics and Dentofacial Orthopedics (Uttar Pradesh, India).ORCID http://orcid.org/0000-0001-7894-1378

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess whether there is any difference in the genetic association between Class II division 1 (div. 1) and division 2 (div. 2) malocclusions using PAX9 (rs8004560) gene single nucleotide polymorphism (SNP). MATERIAL AND

methodsSixty patients from the Orthodontics department of Subharti Dental College and Hospital (Meerut, India) were divided into two groups: Group 1 (Class II div. 1 malocclusion) and Group 2 (Class II div. 2 malocclusion). Then, 3 mL of blood was collected from each participant. DNA extraction was done, and Sanger Sequencing was performed from extracted DNA samples.

resultsA statistically significant difference was found in the distribution of alleles among Class II div. 1 and Class II div. 2 malocclusions. The homozygous GG allele was the most prevalent among Class II div. 1 patients (76.7%), while the heterozygous AG allele was the most prevalent among Class II div. 2 patients (53.5%). Since GG was the most prevalent allele, it was used as a reference, and AA/AG were compared with GG to confirm the association. The results showed that individuals with the AG genotype seemed to be more susceptible to the development of skeletal Class II div. 2 malocclusion.

conclusionThe homozygous GG allele was the most prevalent among Class II div. 1 patients, while the heterozygous AG allele was the most prevalent among Class II div. 2 patients, suggesting that there could be a difference between the genetic association of both malocclusions.

Indexed as

Malocclusion, Angle Class IIPAX9 Transcription FactorPolymorphism, Single NucleotideAdolescentAllelesChildFemaleGenotypeHumansIndiaMaleTertiary Care CentersPAX9 protein, humanPAX9 Transcription Factor

Identifiers

PMID39699986
PMCPMC11655015

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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.