Related Experiment Video
Updated: Jun 24, 2025

05:25
Author Spotlight: Comparing Alveolar and Long Bone Remodeling to Explore OTM Model Potential
Published on: July 21, 2023
1.4K
Genetic polymorphisms linked to extreme postorthodontic external apical root resorption in Koreans
Jing Liu1, Kwanwoo Park2, Yoon Jeong Choi1
1Department of Orthodontics, Institute of Craniofacial Deformity, Yonsei University College of Dentistry, Seoul, Korea.
Progress in Orthodontics
|June 9, 2024
Summary
Genetic variations in specific genes are linked to severe external apical root resorption (EARR) during orthodontic treatment in Koreans. This research aids in developing tools to predict significant EARR risk.
Area of Science:
- Genetics
- Orthodontics
- Dental Research
Background:
- External apical root resorption (EARR) is a frequent complication of orthodontic therapy.
- Identifying genetic factors influencing extreme EARR is crucial for patient management.
Purpose of the Study:
- To identify genetic polymorphisms associated with susceptibility to extreme orthodontic-induced EARR in a Korean population.
- Utilize extreme phenotype analysis for targeted genetic investigation.
Main Methods:
- Genomic DNA was extracted from saliva of 77 orthodontic patients.
- Patients were categorized into significant resorption (≥4 mm) and normal (<2 mm) groups.
- Targeted next-generation sequencing and logistic regression analyzed single nucleotide polymorphisms (SNPs) and haplotypes.
Main Results:
- Eleven SNPs in genes TNFSF11, TNFRSF11B, WNT3A, SFRP2, LRP6, P2RX7, and LRP1 showed significant association with severe EARR (p<0.05).
- A specific P2RX7 haplotype (CCA) was more frequent in the severe resorption group.
Conclusions:
- Extreme phenotype analysis successfully identified genetic markers linked to severe EARR in the Korean population.
- These findings support the development of predictive diagnostic tools for severe root resorption during orthodontics.
Related Concept Videos
Single Nucleotide Polymorphisms-SNPs
15.0K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.0K
Teeth
383
The formation of teeth, also known as odontogenesis, is a complex process that begins in utero, around the sixth week of embryonic development. There are three stages to this process: the bud stage, the cap stage, and the bell stage.
In the bud stage, the tooth germ (an aggregation of cells) starts to form in the developing jawbone. During the cap stage, the tooth germ differentiates into enamel organ, dental papilla, and dental sac, which will later develop into the tooth's enamel, dentin...
In the bud stage, the tooth germ (an aggregation of cells) starts to form in the developing jawbone. During the cap stage, the tooth germ differentiates into enamel organ, dental papilla, and dental sac, which will later develop into the tooth's enamel, dentin...
383

