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Published on: February 13, 2021
Epigenetic Connections in Malocclusion
Elzbieta Pawlowska1, Maria Mitus-Kenig2, Janusz Blasiak3
1Department of Pediatric Dentistry, Medical University of Lodz, 92-213 Lodz, Poland.
Epigenetic mechanisms, like DNA methylation, influence craniofacial development and tooth movement. However, direct evidence linking specific epigenetic changes to malocclusion in humans is currently lacking for clinical use.
Area of Science:
- Genetics and Developmental Biology
- Orthodontics and Dental Research
- Epigenetics
Background:
- Malocclusion results from genetic, environmental, and developmental factors.
- Epigenetic mechanisms (DNA methylation, histone modifications, non-coding RNAs) are implicated in craniofacial growth and dentoalveolar remodeling.
- Existing evidence is largely indirect, derived from in vitro studies, animal models, and related craniofacial processes.
Purpose of the Study:
- To critically evaluate the current evidence on the role of epigenetic regulation in malocclusion development.
- To assess the role of epigenetics in orthodontic tooth movement.
- To identify gaps in research and guide future clinical translation.
Main Methods:
- Structured narrative review.
- Qualitative appraisal framework considering study design, methodological rigor, and evidence directness.
- Analysis of experimental findings on epigenetic regulation by mechanical forces.
Main Results:
- Epigenetic mechanisms are dynamically regulated by mechanical forces, influencing key cellular processes like osteogenesis and chondrogenesis.
- Individual variability in orthodontic response may be linked to epigenetic factors.
- Robust causal studies directly linking specific epigenetic modifications to human malocclusion phenotypes are lacking.
Conclusions:
- While biologically plausible, a significant gap exists between current mechanistic insights into epigenetics and their clinical application in orthodontics.
- The clinical utility of epigenetic markers for diagnosing, treating, or predicting malocclusion outcomes is currently limited.
- Future research requires well-designed longitudinal human studies correlating epigenetic profiles with defined malocclusion phenotypes to establish causality and enable clinical relevance.
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