Literature DB >> 28969278

Expressional Analysis of MSX1 (Human) Revealed its Role in Sagittal Jaw Relationship.

Prateek Gupta1, Thakur Prasad Chaturvedi2, Vipul Sharma3.   

Abstract

INTRODUCTION: Abnormal skeletal jaw relationships is an important factor causing difficulty in speech, mastication, sleep and social interaction, thus affect the overall well being of an individual. AIM: The present study was an attempt to decipher the role of human MSX1 in terms of sagittal jaw relationship by employing Polymerase Chain Reaction (PCR) based analysis.
MATERIALS AND METHODS: Ninety-eight case subjects belonging to North India with skeletal Class II and Class III jaw relationships were selected. Further, thirty-five control subjects of the same region having Class I skeletal and dental relationships (normal Jaw relationships) with good alignment of all teeth were enrolled. MSX1 gene sequencing was performed using the subjects' blood samples. Multiple sequence alignment was performed to find Single Nucleotide Polymorphisms (SNP's). Nine SNP's were obtained of which seven were reported and two novels. Statistical analysis was performed using Chi square test to compare genotype differences between case and control groups.
RESULTS: SNP rs186861426 was found to be significantly associated in Class I subjects (p-value=0.02). The sequencing results suggested that individuals having changes from G (guanosine) with A (adenine) genotype had approximately seven times low risk for developing Class II division 1 malocclusion as compared to those alleles having GG genotype and therefore, allele 'A' position on chromosome 4 (rs186861426) seems to have a protective role.
CONCLUSION: The study unfolds an important relationship between MSX1 gene and Class II division 1 malocclusion and Class I normal skeletal relationships. The study tried to interpret the role of human MSX1 and extend the gene pool responsible for the skeletal anomalies related to development of abnormal upper and lower jaws.

Entities:  

Keywords:  Gene; Genetics; Malocclusion; Prognathic jaw

Year:  2017        PMID: 28969278      PMCID: PMC5620925          DOI: 10.7860/JCDR/2017/26755.10441

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


  47 in total

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Journal:  J Hum Genet       Date:  2006-07-26       Impact factor: 3.172

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  3 in total

1.  Three-dimensional palatal anatomic characteristics' correlation with dermatoglyphic heterogeneity in Angle malocclusions.

Authors:  Ibrahim AlShahrani; Ali A Dawasaz; Sadatullah Syed; Mohammed Ibrahim; Rafi A Togoo
Journal:  Angle Orthod       Date:  2019-03-06       Impact factor: 2.079

Review 2.  Genetic factors contributing to skeletal class III malocclusion: a systematic review and meta-analysis.

Authors:  Alexandra Dehesa-Santos; Paula Iber-Diaz; Alejandro Iglesias-Linares
Journal:  Clin Oral Investig       Date:  2021-02-07       Impact factor: 3.573

3.  Genes and Pathways Associated with Skeletal Sagittal Malocclusions: A Systematic Review.

Authors:  Elizabeth Gershater; Chenshuang Li; Pin Ha; Chun-Hsi Chung; Nipul Tanna; Min Zou; Zhong Zheng
Journal:  Int J Mol Sci       Date:  2021-12-02       Impact factor: 5.923

  3 in total

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