Abstract

BackgroundThis study aimed to investigate the genetic association of specific Single Nucleotide Polymorphisms (SNPs) within the muscle segment homeobox gene 1 (MSX1) with susceptibility to the peg-shaped teeth in 36 Jordanian Arab families and case–control samples in the Jordanian Arab population.MethodsThis cohort involved 108 individuals (36 trios families), which were used for family-based genetic study. Additionally, 56 patients and 57 controls were used for case–control study. Genomic DNA samples from both families and case–control were extracted according to distinguished processes. Then, polymerase chain reaction technique (PCR) was conducted using specific primers for the axons of the MSX1. Moreover, DNA sequencing genotyping method analysis of SNPs was used to detect specified SNPs in the MSX1 linked with peg-shaped teeth. Hardy–Weinberg Equilibrium and Chi-square were used to evaluate the data quality and the presence of any genotypic error. In addition, Transmission Disequilibrium Test (TDT) was used identify family-based association in which trios of parents and proband are used.ResultsThe results of this study showed fourteen polymorphic sites in this gene, eight of them (rs121913129, rs104893852, rs104893853, rs121913130, rs104893850, rs1095, rs3775261, and rs1042484) were none-polymorphic. Meanwhile, the minor allele frequencies of the rest of the SNPs were polymorphic (rs8670, rs12532, rs3821949, rs4464513, rs1907998, and rs6446693). However, none of these SNPs were associated with peg-shaped teeth. Moreover, the haplotype genetic analysis revealed that there was no genetic association with peg-shaped teeth disorder susceptibility (P > 0.05) in the Jordanian families of Arab descent.ConclusionsThe present findings can be used in estimation of prevalence of peg-shaped teeth in the Jordanian population. However, our findings revealed that there is no evidence that the MSX1 polymorphisms had a crucial role in the peg-shaped teeth phenomenon, emphasizing that other genes might have this role. These findings are beneficial for clinicians to comprehensively understand the molecular aspects of teeth abnormalities.

Highlights

  • This study aimed to investigate the genetic association of specific Single Nucleotide Polymorphisms (SNPs) within the muscle segment homeobox gene 1 (MSX1) with susceptibility to the peg-shaped teeth in 36 Jorda‐ nian Arab families and case–control samples in the Jordanian Arab population

  • The objective of this study was to investigate the genetic association of the MSX1 and its susceptibility to the peg-shaped teeth in 36 families and case–control samples Jordanian Arab population

  • Participants Ethical approval for this study was in compliance with the Institutional Review Board (IRB) Guidelines at Jordan University of Science and Technology (IRB# 19/85/2015)

Read more

Summary

Introduction

This study aimed to investigate the genetic association of specific Single Nucleotide Polymorphisms (SNPs) within the muscle segment homeobox gene 1 (MSX1) with susceptibility to the peg-shaped teeth in 36 Jorda‐ nian Arab families and case–control samples in the Jordanian Arab population. Alkhatib et al BMC Oral Health (2022) 22:16 teeth affected are the upper lateral incisors or sometimes third molars. It might be seen on both sides in most instances, and they have shorter roots than usual teeth [2]. Hua et al [7] reported that women were 1.35 times more likely than men to have peg-shaped maxillary permanent upper lateral incisors. The prevalence of peg-shaped teeth is about 1.8% [7]. The prevalence of tooth agenesis in permanent teeth in both genders varies among different populations. The prevalence was the highest in Australia (males 5.5% and females 7.6%) [8]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call