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1.
Int Orthod ; 17(3): 529-537, 2019 09.
Article in English | MEDLINE | ID: mdl-31279755

ABSTRACT

PURPOSE: To use 3-dimensional cone beam computed tomography (CBCT) images obtained on patients before treatment with dental malocclusion to calculate the heritability estimates of full-tooth angulation and inclination. A heritability estimate is a number between zero and one indicating the percentage of genetic factors involved in determining the phenotypic variation observed. METHOD: CBCT images of 111 patients (51 sibships) were analysed measuring both tooth angulation and inclination using the Anatomage Invivo5 software for central incisor to second molar. The long axis of each tooth was defined and traced as the cusp tip of the most mesiobuccal cusp to 6mm coronal to the apex of the mesiobuccal root. SPSS statistical software was used to analyse the data and calculate the heritability estimates for each tooth type in the maxilla and in the mandible regardless of the side. RESULTS: Teeth inclination showed higher heritability estimates than tooth angulation. Furthermore, maxillary teeth showed higher heritability estimates than mandibular teeth and anterior teeth showed higher heritability than posterior teeth. CONCLUSION: Genetic effect was more evident on tooth inclination than tooth angulation, on anterior teeth more than posterior teeth, and on maxillary teeth more than mandibular teeth.


Subject(s)
Malocclusion/pathology , Molar/anatomy & histology , Quantitative Trait, Heritable , Siblings , Adolescent , Child , Cone-Beam Computed Tomography/methods , Female , Humans , Imaging, Three-Dimensional/methods , Male , Malocclusion/diagnostic imaging , Mandible , Maxilla , Orthodontics , Software , Tooth Crown/anatomy & histology , Tooth Root
2.
Am J Orthod Dentofacial Orthop ; 134(6): 742-50, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19061800

ABSTRACT

INTRODUCTION: External apical root resorption (EARR) is an unwanted sequelae of orthodontic treatment. Genetic factors account for approximately 64% of the EARR variation in humans. Inbred mice offer a model to control the environmental factors and genetic heterogeneity that complicate human genetic studies. Genetically distinct inbred mice and their offspring (F1s) were analyzed to examine the mode of inheritance and the influence of parental sex on the susceptibility to root resorption associated with orthodontic force (RRAOF). METHODS: RRAOF was determined histologically for male and female mice of the A/J, DBA/2J, and BALB/cJ strains, and the A/JxDBA/2J and A/JxBALB/cJ crosses (10 males and 10 females/reciprocal cross). RRAOF was induced by tipping the maxillary first molar mesially for 9 days. RESULTS: Sex differences were observed only among the mice of the BALB/cJ strain. Two patterns of inheritance were observed; F1s from the A/JxBALB/cJ cross were resistant, suggesting that the A/J have dominant resistance alleles. On the other hand, F1s from the A/JxDBA/2J cross showed RRAOF intermediate between their parental mice, suggesting a polygenic trait. CONCLUSIONS: These results provide evidence of a traceable and polygenetic component affecting RRAOF in mice.


Subject(s)
Genetic Predisposition to Disease/genetics , Root Resorption/genetics , Tooth Movement Techniques/adverse effects , Acid Phosphatase/analysis , Alleles , Animals , Biomarkers/analysis , Crosses, Genetic , Disease Models, Animal , Female , Genes, Dominant/genetics , Isoenzymes/analysis , Male , Mice , Mice, Inbred A , Mice, Inbred BALB C , Mice, Inbred DBA , Mice, Inbred Strains , Molar/pathology , Multifactorial Inheritance/genetics , Sex Factors , Stress, Mechanical , Tartrate-Resistant Acid Phosphatase
3.
Eur J Orthod ; 28(1): 13-9, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16373453

ABSTRACT

Root resorption (RR) is an unwanted sequela of orthodontic treatment. Despite rigorous investigation, no single factor or group of factors that directly causes RR has been identified. The purpose of this study was to examine the effect of the genotype on susceptibility or resistance to develop RR secondary to orthodontic force. Nine-week-old male mice from eight inbred strains were used and randomly distributed into control (C) or treatment (T) groups as follows: A/J (C = 9,T = 9), C57BL/6J (C = 7,T = 8), C3H/HeJ (C = 8,T = 6), BALB/cJ (C = 8,T = 6), 129P3/J (C = 6,T = 8), DBA/2J (C = 8,T = 9), SJL/J (C = 8,T = 10), and AKR/J (C = 9,T = 8). Each of the treated mice received an orthodontic appliance to tip the maxillary left first molar mesially for 9 days. Histological sections of the tooth were used to determine RR and tartrate resistant acid phosphatase (TRAP) activity. The Wilcoxon ranked-sum non-parametric test was used to evaluate differences between the groups. The results showed that the DBA/2J, BALB/cJ, and 129P3/J inbred mouse strains are highly susceptible to RR, whereas A/J, C57BL/6J and SJL/J mice are much more resistant. The variation in the severity of RR associated with orthodontic force among different inbred strains of mice when age, gender, food, housing, and orthodontic force magnitude/duration are controlled support the hypothesis that susceptibility or resistance to RR associated with orthodontic force is a genetically influenced trait.


Subject(s)
Root Resorption/etiology , Root Resorption/genetics , Tooth Movement Techniques/adverse effects , Acid Phosphatase/metabolism , Animals , Biomarkers/metabolism , Dental Stress Analysis , Disease Models, Animal , Genetic Predisposition to Disease/genetics , Genotype , Isoenzymes/metabolism , Male , Mice , Mice, Inbred Strains , Random Allocation , Reproducibility of Results , Tartrate-Resistant Acid Phosphatase
4.
Am J Orthod Dentofacial Orthop ; 123(3): 242-52, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12637896

ABSTRACT

External apical root resorption (EARR) can be an undesirable sequela of orthodontic treatment. Previous studies have suggested that EARR has a substantial genetic component. Linkage and association were examined between polymorphisms of the interleukin IL-1 (IL-1A and IL-1B) genes and EARR in 35 white American families. Buccal swab cells were collected for DNA isolation and analysis. The EARR in the maxillary central incisors, the mandibular central incisors, and the mesial and distal roots of the mandibular first molar were analyzed separately and together by using both linkage and association methods of analysis. Highly significant (P =.0003) evidence of linkage disequilibrium of IL-1B polymorphism with the clinical manifestation of EARR was obtained. The analysis indicates that the IL-1B polymorphism accounts for 15% of the total variation of maxillary incisor EARR. Persons homozygous for the IL-1B allele 1 have a 5.6 fold (95% CI 1.9-21.2) increased risk of EARR greater than 2 mm as compared with those who are not homozygous for the IL-1 beta allele 1. Data indicate that allele 1 at the IL-1B gene, known to decrease the production of IL-1 cytokine in vivo, significantly increases the risk of EARR. These findings are consistent with an interpretation of EARR as a complex condition influenced by many factors, with the IL-1B gene contributing an important predisposition to this common problem. Defining genetic contributions to EARR is an important factor in understanding the contribution of environmental factors, such as habits and therapeutic biomechanics.


Subject(s)
Genetic Predisposition to Disease/genetics , Root Resorption/genetics , Alleles , Child , Chromosomes, Human, Pair 2/genetics , Female , Humans , Interleukin-1/biosynthesis , Interleukin-1/genetics , Linkage Disequilibrium , Male , Orthodontics, Corrective/adverse effects , Parents , Pedigree , Polymorphism, Restriction Fragment Length , Regression Analysis , Root Resorption/etiology , Root Resorption/metabolism , Siblings , White People/genetics
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