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1.
Gen Dent ; 72(2): 48-54, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38411485

RESUMEN

The purpose of this research was to test the reliability of a modified magnification method for determining the position of an impacted canine from a single panoramic radiograph. This retrospective study evaluated 114 panoramic radiographs showing 136 impacted maxillary canines. The widths of the impacted canines, contralateral erupted canines, and ipsilateral maxillary incisors were measured, and ratios for the canine-incisor index (CII) and canine-canine index (CCI) were calculated. The impacted canines were also classified according to their location in the vertical plane (apical, middle, or coronal zone) relative to the contralateral central incisor. Continuous data were analyzed for normal distribution, and logistic and multivariate logistic regression models were conducted. The Benjamini-Hochberg procedure with a false discovery rate of 0.05 was used to account for multiple testing. The intrarater reliability was excellent for impacted canine, central incisor, and contralateral canine measurements (intraclass correlation coefficient > 0.9). The CII and vertical zone were strong predictors of an impacted canine position with clinically useful sensitivity and specificity values (0.69 and 0.74, respectively, based on an area under the curve concordance statistic of 0.75). A predictive range was evident for the CII of palatally (1.10-1.39) and buccally (0.90-1.19) impacted canines in the middle and coronal zones, respectively. The occurrence of palatal or buccal positioning was not significantly associated with the CCI (P = 0.2). The CII and vertical zone identified from a single panoramic radiograph can be used to determine the buccopalatal position of an impacted canine, with more reliability if the impacted canine crown is in the middle or coronal zone of the contralateral central incisor.


Asunto(s)
Diente Impactado , Humanos , Radiografía Panorámica , Reproducibilidad de los Resultados , Estudios Retrospectivos , Diente Impactado/diagnóstico por imagen , Diente Canino/diagnóstico por imagen
2.
Am J Orthod Dentofacial Orthop ; 163(3): 357-367.e3, 2023 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-36503861

RESUMEN

INTRODUCTION: Recent 3-dimensional technology advancements have resulted in new techniques to improve the accuracy of intraoperative transfer. This study aimed to validate the accuracy of computer-aided design and manufacturing (CAD-CAM) customized surgical cutting guides and fixation plates on mandibular repositioning surgery performed in isolation or combined with simultaneous maxillary repositioning surgery. METHODS: Sixty patients who underwent mandibular advancement surgery by the same surgeon were retrospectively evaluated by 3-dimensional surface-based superimposition. A 3-point coordinate system (x, y, z) was used to identify the linear and angular discrepancies between the planned movements and actual outcomes. Wilcoxon rank sum test was used to compare the outcomes between the mandible-only and the bimaxillary surgery groups with significance at P <0.05. Pearson correlation coefficient compared planned mandible advancement to the outcome from advancement planned. The centroid, which represents the mandible as a single unit, was computed from 3 landmarks, and the discrepancies were evaluated by the root mean square error (RMSE) for clinical significance set at 2 mm for linear discrepancies and 4° for angular discrepancies. RESULTS: There was no statistically significant difference between the planned and actual position of the mandible in either group when considering absolute values of the differences. When considering raw directional data, a statistically significant difference was identified in the y-axis suggesting a tendency for under-advancement of the mandible in the bimaxillary group. The largest translational RMSE for the centroid was 0.77 mm in the sagittal dimension for the bimaxillary surgery group. The largest rotational RMSE for the centroid was 1.25° in the transverse dimension for the bimaxillary surgery group. Our results show that the precision and clinical feasibility of CAD-CAM customized surgical cutting guides and fixation plates on mandibular repositioning surgery is well within clinically acceptable parameters. CONCLUSION: Mandibular repositioning surgery can be performed predictably and accurately with the aid of CAD-CAM customized surgical cutting guides and fixation plates with or without maxillary surgery.


Asunto(s)
Procedimientos Quirúrgicos Ortognáticos , Cirugía Asistida por Computador , Humanos , Estudios Retrospectivos , Cirugía Asistida por Computador/métodos , Imagenología Tridimensional , Procedimientos Quirúrgicos Ortognáticos/métodos , Diseño Asistido por Computadora
3.
Semin Orthod ; 23(4): 336-347, 2017 12.
Artículo en Inglés | MEDLINE | ID: mdl-29290679

RESUMEN

Uncovering the genetic factors that correlate with a clinical deviation of previously unknown etiology helps to diminish the unknown variation influencing the phenotype. Clinical studies, particularly those that consider the effects of an appliance or treatment regimen on growth, need to be a part of these types of genetic investigations in the future. While the day-to-day utilization of "testing" for genetic factors is not ready for practice yet, genetic testing for monogenic traits such as Primary Failure of Eruption (PFE) and Class III malocclusion is showing more promise as knowledge and technology advances. Although the heterogeneous complexity of such things as facial and dental development, the physiology of tooth movement, and the occurrence of External Apical Root Resorption (EARR) make their precise prediction untenable, investigations into the genetic factors that influence different phenotypes, and how these factors may relate to or impact environmental factors (including orthodontic treatment) are becoming better understood. The most important "genetic test" the practitioner can do today is to gather the patient's individual and family history. This would greatly benefit the patient, and augment the usefulness of these families in future clinical research in which clinical findings, environmental, and genetic factors can be studied.

4.
Periodontol 2000 ; 72(1): 54-75, 2016 10.
Artículo en Inglés | MEDLINE | ID: mdl-27501491

RESUMEN

The increased prevalence and severity of periodontal disease have long been associated with aging, such that this oral condition affects the majority of the adult population over 50 years of age. Although the immune system is a critical component for maintaining health, aging can be characterized by quantitative and qualitative modifications of the immune system. This process, termed 'immunosenescence', is a progressive modification of the immune system that leads to greater susceptibility to infections, neoplasia and autoimmunity, presumably reflecting the prolonged antigenic stimulation and/or stress responses that occur across the lifespan. Interestingly, the global reduction in the host capability to respond effectively to these challenges is coupled with a progressive increase in the general proinflammatory status, termed 'inflammaging'. Consistent with the definition of immunosenescence, it has been suggested that the cumulative effect of prolonged exposure of the periodontium to microbial challenge is, at least in part, a contributor to the effects of aging on these tissues. Thus, it has also been hypothesized that alterations in the function of resident immune and nonimmune cells of the periodontium contribute to the expression of inflammaging in periodontal disease. Although the majority of aging research has focused on the adaptive immune response, it is becoming increasingly clear that the innate immune compartment is also highly affected by aging. Thus, the phenomenon of immunosenescence and inflammaging, expressed as age-associated changes within the periodontium, needs to be more fully understood in this era of precision and personalized medicine and dentistry.


Asunto(s)
Envejecimiento/inmunología , Inflamación/inmunología , Enfermedades Periodontales/inmunología , Inmunidad Adaptativa/inmunología , Envejecimiento/fisiología , Enfermedades Autoinmunes/complicaciones , Enfermedades Autoinmunes/inmunología , Autoinmunidad/inmunología , Citocinas/genética , Citocinas/inmunología , Susceptibilidad a Enfermedades/inmunología , Epigenómica , Humanos , Sistema Inmunológico , Inmunidad Innata/genética , Inmunidad Innata/inmunología , Inmunosenescencia/fisiología , Neoplasias/complicaciones , Neoplasias/inmunología , Periodoncio/inmunología , Periodoncio/microbiología , Polimorfismo Genético
5.
J Endod ; 50(6): 758-765, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-38513792

RESUMEN

INTRODUCTION: Orthognathic surgery has the potential to compromise the vitality of the teeth. This paper aims to assess changes in pulp blood flow (PBF) and pulp sensibility (PS) of the anterior dentition following orthognathic surgery and to assess the influence of the proximity of the surgical osteotomy on the PBF and/or PS. METHODS: Twenty-six patients undergoing orthognathic surgery (Le Fort I or bilateral sagittal split osteotomy [BSSO]) were compared to sixteen control patients treated by fixed appliances only using Laser Doppler flowmeter (LDF) and thermal testing (CO2 snow). Surgery patients were tested at T1 (presurgery), T2 (4-5 weeks postsurgery), T3 (3 months postsurgery), and T4 (6 months postsurgery). Control patients were tested at T1 (pretreatment), T2 (6 months posttreatment), T3 (12 months posttreatment), and T4 (18 months posttreatment). Differences between the maxilla and mandible were assessed. RESULTS: No differences in PBF or PS were recorded in the control group. In the surgery group, both jaws followed the same pattern after surgery, an initial decrease at T2 followed by a gradual recovery to pretreatment PBF levels with no significant difference between T1 versus T4 in both jaws. No difference in PBF was observed between the maxilla and mandible at any testing time interval. CONCLUSIONS AND CLINICAL IMPLICATIONS: PBF and PS of the anterior dentition was severely affected immediately postsurgery, followed by a gradual increase to full recovery. This pattern of recovery was exhibited in both jaws. A negative sensibility response or discoloration should not be seen as an indication of irreversible ischemic pulp changes. Monitoring for at least 6 months or using LDF as a confirmatory test is required before any irreversible endodontic treatment is to be considered.


Asunto(s)
Pulpa Dental , Flujometría por Láser-Doppler , Procedimientos Quirúrgicos Ortognáticos , Humanos , Pulpa Dental/irrigación sanguínea , Pulpa Dental/fisiología , Estudios Prospectivos , Femenino , Masculino , Adulto , Adulto Joven , Flujo Sanguíneo Regional/fisiología , Adolescente , Osteotomía Le Fort , Osteotomía Sagital de Rama Mandibular/métodos , Mandíbula/cirugía , Mandíbula/irrigación sanguínea
6.
Angle Orthod ; 93(6): 675-682, 2023 11 01.
Artículo en Inglés | MEDLINE | ID: mdl-37407506

RESUMEN

OBJECTIVES: To evaluate gingival phenotype (GP) and thickness (GT) using visual, probing, and ultrasound (US) methods and to assess the accuracy and consistency of clinicians to visually identify GP. MATERIALS AND METHODS: The GP and GT of maxillary and mandibular anterior teeth in 29 orthodontic patients (mean age 25 ± 7.5 years) were assessed using probing and US by a single examiner. General dentist and dental specialist assessors (n = 104) were shown intraoral photographs of the patients, including six repeated images, and asked to identify the GP via a questionnaire. RESULTS: An increasing trend in GT values of thin, medium, and thick biotype probe categories was found, though this was not statistically significant (P = .188). Comparison of probing method to determinations of GT made by US yielded slight agreement (κ = 0.12). Using the visual method, assessors' identification of the second GP determination ranged from poor to moderate agreement (κ = 0.29 to κ = 0.53). CONCLUSIONS: The probe method is sufficient in differentiating between different categories of GP. However, further research is required to assess the sensitivity of the probe method in recognizing phenotypes in the most marginal of cases. Assessors using the visual method lack the ability to identify GP accurately and consistently among themselves.


Asunto(s)
Encía , Incisivo , Humanos , Adolescente , Adulto Joven , Adulto , Encía/diagnóstico por imagen , Maxilar , Fotografía Dental , Ultrasonido , Fenotipo
7.
Angle Orthod ; 93(5): 545-551, 2023 09 01.
Artículo en Inglés | MEDLINE | ID: mdl-37145979

RESUMEN

OBJECTIVES: To investigate the association between the width of keratinized gingiva (WKG), gingival phenotype (GP), and gingival thickness (GT) with craniofacial morphology in sagittal and vertical dimensions. MATERIALS AND METHODS: WKG, GP, and GT of mandibular anterior teeth in 177 preorthodontic patients (mean age 18.38 ± 5.16 years) were assessed clinically using a periodontal probe, a Colorvue Biotype Probe, and ultrasound by a single examiner. Patients were grouped into skeletal Class I, II, and III and hyperdivergent, normodivergent, and hypodivergent based on ANB and SN-MP angles. Mandibular incisor inclination (L1-NB) was also measured. Clinical and cephalometric measurements were repeated to assess inter- and intraexaminer reproducibility. RESULTS: A significant association was found between thin GP and skeletal Classes I and III for the left mandibular central incisor (MCI; P = .0183). In skeletal Class III patients, L1-NB angle demonstrated a decreasing trend as phenotype thickness decreased. A significant association was found between thin phenotype and normodivergent and hypodivergent groups for MCIs (left: P = .0009, right: P = .00253). No significant association between WKG or GT and craniofacial morphology was found. CONCLUSIONS: Thin GP is associated with skeletal Class I and III for the left MCI. Thin GP is associated with hypodivergent and normodivergent skeletal patterns for the MCIs. There was no association between WKG and GT and craniofacial morphology in both skeletal and vertical dimensions. Dental compensations that exist due to different craniofacial morphology may influence the GP.


Asunto(s)
Encía , Incisivo , Encía/diagnóstico por imagen , Incisivo/diagnóstico por imagen , Incisivo/anatomía & histología , Reproducibilidad de los Resultados , Mandíbula/diagnóstico por imagen , Mandíbula/anatomía & histología , Cefalometría
8.
Front Pediatr ; 11: 1117493, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37441579

RESUMEN

Pediatric obstructive sleep apnea (POSA) is a complex disease with multifactorial etiopathogenesis. The presence of craniofacial dysmorphisms influencing the patency of the upper airway is considered a risk factor for POSA development. The craniofacial features associated with sleep-related breathing disorders (SRBD) - craniosynostosis, retrognathia and micrognathia, midface and maxillary hypoplasia - have high heritability and, in a less severe form, could be also found in non-syndromic children suffering from POSA. As genetic factors play a role in both POSA and craniofacial dysmorphisms, we hypothesize that some genes associated with specific craniofacial features that are involved in the development of the orofacial area may be also considered candidate genes for POSA. The genetic background of POSA in children is less explored than in adults; so far, only one genome-wide association study for POSA has been conducted; however, children with craniofacial disorders were excluded from that study. In this narrative review, we discuss syndromes that are commonly associated with severe craniofacial dysmorphisms and a high prevalence of sleep-related breathing disorders (SRBD), including POSA. We also summarized information about their genetic background and based on this, proposed 30 candidate genes for POSA affecting craniofacial development that may play a role in children with syndromes, and identified seven of these genes that were previously associated with craniofacial features risky for POSA development in non-syndromic children. The evidence-based approach supports the proposition that variants of these candidate genes could lead to POSA phenotype even in these children, and, thus, should be considered in future research in the general pediatric population.

9.
Am J Orthod Dentofacial Orthop ; 142(5): 662-70, 2012 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-23116507

RESUMEN

INTRODUCTION: Sagittal jaw growth is influenced during puberty by a ratio of androgens and estrogens. The CYP19A1 (formerly CYP19) gene encodes the cytochrome P450 enzyme aromatase (estrogen synthetase), which converts testosterone to estrogen. Genetic variations including single nucleotide polymorphisms might regulate CYP19A1 gene expression or the function of the aromatase protein and thus influence sagittal jaw growth. METHODS: The annual sagittal jaw growth in 92 pubertal orthodontic patients was determined by using pretreatment and posttreatment cephalometric radiographs. Single nucleotide polymorphisms rs2470144 and rs2445761 were genotyped and haplotypes constructed. Associations between genotypes or haplotypes and the annual sagittal growth were estimated by using JMP (version 9.0; SAS Institute, Cary, NC). RESULTS: Two single nucleotide polymorphisms were significantly associated with average differences in annual sagittal jaw growth in boys. Haplotype analysis demonstrated that haplotypes T(rs2470144)T(rs2445761) and C(rs2470144)T(rs2445761) had significant effects on annual sagittal maxillary growth and on mandibular growth in boys. No association was found in girls. CONCLUSIONS: A quantitative trait locus that influences male pubertal sagittal jaw growth might exist in the CYP19A1 gene, and single nucleotide polymorphisms rs2470144 and rs2445761 might be inside this quantitative trait locus or be linked to it.


Asunto(s)
Aromatasa/genética , Mandíbula/crecimiento & desarrollo , Maxilar/crecimiento & desarrollo , Desarrollo Maxilofacial/genética , Pueblo Asiatico/genética , Cefalometría , Niño , China , Femenino , Frecuencia de los Genes , Haplotipos , Humanos , Análisis de los Mínimos Cuadrados , Modelos Lineales , Desequilibrio de Ligamiento , Masculino , Mandíbula/anatomía & histología , Maxilar/anatomía & histología , Polimorfismo de Nucleótido Simple , Reproducibilidad de los Resultados , Factores Sexuales
10.
Am J Orthod Dentofacial Orthop ; 140(4): 520-6, 2011 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-21967939

RESUMEN

INTRODUCTION: Little research has been conducted to evaluate protocols and trends in orthodontic retention. The purpose of this study was to identify the general retention protocols used by orthodontists in the United States. Additionally, our goal was to identify trends in these orthodontic retention protocols by evaluating how they have changed over the past 5 years and how they might continue to change in the next 5 years. METHODS: The study was conducted via a 36-question electronic survey (REDCap, Nashville, Tenn) with branching logic on certain questions. The survey was sent to all 9143 practicing members of the American Association of Orthodontists in the United States, and 1632 (18%) responded. RESULTS AND CONCLUSIONS: Mean retention protocols of the surveyed population showed predominant use of Hawley or vacuum-formed retainers in the maxillary arch and fixed retention in the mandibular arch. For both arches, there is a current shift away from Hawley retainers and toward vacuum-formed retainers and fixed retention. Respondents who extract fewer teeth reported increased use of fixed retention in the maxillary (P = 0.041) and mandibular (P = 0.003) arches. Respondents who extract fewer teeth and use removable retainers were more likely to tell their patients to wear their retainers at night for the rest of their lives (P = 1.63 × 10(-6)).


Asunto(s)
Retenedores Ortodóncicos/estadística & datos numéricos , Ortodoncia/estadística & datos numéricos , Pautas de la Práctica en Odontología/estadística & datos numéricos , Protocolos Clínicos , Arco Dental , Femenino , Humanos , Internet , Masculino , Mandíbula , Maxilar , Diseño de Aparato Ortodóncico/estadística & datos numéricos , Diseño de Aparato Ortodóncico/tendencias , Retenedores Ortodóncicos/clasificación , Retenedores Ortodóncicos/tendencias , Ortodoncia/tendencias , Cooperación del Paciente , Pautas de la Práctica en Odontología/tendencias , Sociedades Odontológicas , Encuestas y Cuestionarios , Estados Unidos
11.
Pediatr Dent ; 33(3): 221-7, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21703074

RESUMEN

PURPOSE: The purpose of this study was to compare chronologic and dental age using Demirjian's method. METHODS: Two hundred and fifty-seven panoramic radiographs of healthy 5- to 17.5-year-old Caucasian children in the Indianapolis area were evaluated using Demirjian's 7 tooth method. RESULTS: The intraclass correlation coefficient (ICC) for agreement with Demirjian was 0.94 (95% confidence interval [CI]: 0.87, 0.97). The ICC for repeatability of the investigator was 0.97 (95% CI=0.95, 0.99). Calculated dental age was significantly greater than chronologic age by 0.59 years (P<.001). There was no significant difference in the mean difference in ages between sexes (P=.73). Medicaid subjects had a significantly higher (P<.001) mean difference (0.82 years) than private insurance subjects (0.32 years). There was a significant negative correlation between the chronologic age and the difference in ages (r=-0.29, P<.001). Overweight (P<.001) and obese (P=.004) subjects were significantly more dentally advanced than normal (P=.35) and underweight (P=.42) subjects. CONCLUSIONS: Demirjian's method has high inter- and intraexaminer repeatability. Caucasian children in the Indianapolis area are more advanced dentally than the French-Canadian children studied by Demirjian. Difference between dental age and chronologic age varies depending on the age of the child, socioeconomic status, and body mass index.


Asunto(s)
Determinación de la Edad por los Dientes/métodos , Población Blanca , Adolescente , Índice de Masa Corporal , Niño , Preescolar , Femenino , Humanos , Indiana , Seguro Odontológico , Masculino , Medicaid , Obesidad/fisiopatología , Sobrepeso/fisiopatología , Radiografía Panorámica , Reproducibilidad de los Resultados , Clase Social , Estados Unidos
12.
Prog Orthod ; 22(1): 23, 2021 Jul 19.
Artículo en Inglés | MEDLINE | ID: mdl-34278529

RESUMEN

BACKGROUND: The purpose of this study was to identify pretreatment factors associated with the stability of early class III treatment, since most orthodontists start the treatment with their uncertain hypotheses and/or predictions. Subjects consisted of 75 patients with a class III skeletal relationship (ANB < 2° and overjet < 0 mm) who had been consecutively treated with rapid maxillary expansion and facemask and followed until their second phase treatment. The patients were divided into two groups according to whether they showed relapse in follow-up. The stable group maintained their positive overjet (n = 55), and the unstable group experienced relapse with a zero or negative overjet (n = 20). Two general, three dental, and 13 cephalometric pretreatment factors were investigated to determine which factors were associated with stability. RESULTS: Sex, pretreatment age, and anteroposterior functional shift, which were hypothesized as associated factors, were not related to the stability of early class III treatment. Significant differences were detected between the two groups in the horizontal distance between the maxillary and mandibular molars in centric relation. Cephalometric variables, such as the mandibular length (Ar-Me), Wits appraisal, SN to ramus plane angle (SN-Rm), gonial angle, incisor mandibular plane angle (IMPA), and Frankfort plane to mandibular incisor angle (FMIA) showed significant differences between the groups. The horizontal distance was the most influential factor by logistic regression analysis. CONCLUSIONS: Hypothesis (related to sex, age, functional shift) were rejected. Several cephalometric factors related to the mandible were associated with stability. The horizontal distance between the maxillary and mandibular molars in centric relation was the best predictor of early class III treatment relapse.


Asunto(s)
Maloclusión de Angle Clase III , Cefalometría , Aparatos de Tracción Extraoral , Humanos , Maloclusión de Angle Clase III/diagnóstico por imagen , Maloclusión de Angle Clase III/terapia , Mandíbula , Maxilar , Resultado del Tratamiento
13.
Am J Orthod Dentofacial Orthop ; 135(6): 694.e1-16; discussion 694-5, 2009 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-19524819

RESUMEN

INTRODUCTION: The P2X7 receptor plays a crucial role in bone biology and inflammation. Its main function is to promote necrotic tissue metabolism by ensuring a normal acute-phase inflammatory response. We used a mouse model to describe and compare orthodontic mechanotransduction in wild-type and P2X7 knock-out mice. METHODS: By using finite element analysis, mouse orthodontic mechanics were scaled to produce typical human stress levels. External root resorption, bone modeling, and bone remodeling were analyzed with fluorescent bone labels, Masson trichrome stain, and microcomputed tomography. Relationships between the biologic responses and the calculated stresses were statistically tested and compared between mouse types. RESULTS: There were direct relationships between certain stress magnitudes and root resorption and bone formation. Hyalinization and root and bone resorption were different in the 2 types of mice. CONCLUSIONS: Orthodontic responses are related to the principal stress patterns in the periodontal ligament, and the P2X7 receptor plays a significant role in their mechanotransduction.


Asunto(s)
Mecanotransducción Celular/fisiología , Receptores Purinérgicos P2/fisiología , Técnicas de Movimiento Dental/métodos , Animales , Densidad Ósea/fisiología , Remodelación Ósea/fisiología , Resorción Ósea/patología , Resorción Ósea/fisiopatología , Colorantes , Diseño Asistido por Computadora , Modelos Animales de Enfermedad , Análisis de Elementos Finitos , Colorantes Fluorescentes , Humanos , Hialina/fisiología , Imagenología Tridimensional , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Modelos Biológicos , Alambres para Ortodoncia , Osteogénesis/fisiología , Ligamento Periodontal/patología , Ligamento Periodontal/fisiopatología , Distribución Aleatoria , Receptores Purinérgicos P2X7 , Resorción Radicular/etiología , Resorción Radicular/patología , Método Simple Ciego , Estrés Mecánico , Técnicas de Movimiento Dental/instrumentación , Microtomografía por Rayos X
14.
J Orthod ; 36(1): 23-35; discussion 13-4, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19286873

RESUMEN

OBJECTIVE: To compare traditional superimposition on sella turcica and the anterior cranial base (SACB) to superimposition referenced at the occipital condyle (I-point) for demonstrating craniofacial growth and development. MATERIALS AND METHODS: Tracings for ages 8, 10, 12, 15 and 18 were chosen from the Bolton Standards of Dentofacial Developmental Growth to compare superimposition with the traditional longitudinal reference at SACB (anterior curvature of sella turcica and anterior cranial base) to reference at I-point on the antero-inferior contour of the occipital condyles in norma lateralis. The serial tracings were superimposed using both the sagittal and postero-anterior (PA) tracings. Incremental growth of landmarks was measured in relation to Cartesian coordinates and compared between the superimposition methods. RESULTS: Sagittal and PA tracing superimpositions displayed an average 7 mm greater cephalad movement of landmarks, an average 2.4 mm greater ventral movement, and comparable transverse dimension with superimposition referenced at I-point as compared to the SACB reference. CONCLUSION: I-point superimposition demonstrates physiologic growth patterns concealed by traditional registration at sella turcica. The evolution of superimposition on SACB was based on convenience and reproducibility. Fundamental principles of bone development are consistent with the occipital condyles as a more biologic reference for relative craniofacial growth. Actual vertical growth is believed to be greater than displayed in this study, due to the cross-sectional and blended nature of the sample.


Asunto(s)
Cefalometría/normas , Desarrollo Maxilofacial , Adolescente , Niño , Femenino , Humanos , Masculino , Hueso Occipital/crecimiento & desarrollo , Estándares de Referencia , Base del Cráneo/anatomía & histología , Técnica de Sustracción
15.
Hum Mutat ; 29(12): 1392-404, 2008 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18521831

RESUMEN

Within nine dentin dysplasia (DD) (type II) and dentinogenesis imperfecta (type II and III) patient/families, seven have 1 of 4 net -1 deletions within the approximately 2-kb coding repeat domain of the DSPP gene while the remaining two patients have splice-site mutations. All frameshift mutations are predicted to change the highly soluble DSPP protein into proteins with long hydrophobic amino acid repeats that could interfere with processing of normal DSPP and/or other secreted matrix proteins. We propose that all previously reported missense, nonsense, and splice-site DSPP mutations (all associated with exons 2 and 3) result in dominant phenotypes due to disruption of signal peptide-processing and/or related biochemical events that also result in interference with protein processing. This would bring the currently known dominant forms of the human disease phenotype in agreement with the normal phenotype of the heterozygous null Dspp (-/+) mice. A study of 188 normal human chromosomes revealed a hypervariable DSPP repeat domain with extraordinary rates of change including 20 slip-replication indel events and 37 predominantly C-to-T transition SNPs. The most frequent transition in the primordial 9-basepair (bp) DNA repeat was a sense-strand CpG site while a CpNpG (CAG) transition was the second most frequent SNP. Bisulfite-sequencing of genomic DNA showed that the DSPP repeat can be methylated at both motifs. This suggests that, like plants and some animals, humans methylate some CpNpG sequences. Analysis of 37 haplotypes of the highly variable DSPP gene from geographically diverse people suggests it may be a useful autosomal marker in human migration studies.


Asunto(s)
Displasia de la Dentina/genética , Dentinogénesis Imperfecta/genética , Proteínas de la Matriz Extracelular/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Análisis Mutacional de ADN , Humanos , Ratones , Datos de Secuencia Molecular , Fosfoproteínas , Sialoglicoproteínas
16.
Am J Orthod Dentofacial Orthop ; 133(1): 9.e1-13, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18174061

RESUMEN

INTRODUCTION: Clinical cases completed by the Indiana University School of Dentistry (IUSD) graduating orthodontic classes of 2004, 2005, and 2006 were assessed to determine factors that affect orthodontic treatment duration. METHODS: The sample consisted of 455 consecutively finished patients who received comprehensive treatment in the full permanent dentition. They included optimally finished and prematurely terminated (early debond) patients. The American Board of Orthodontics (ABO) discrepancy index (DI) was used to evaluate the severity of the pretreatment malocclusion. A specifically designed treatment complexity index (TCI) was used to evaluate complexity based on treatment modalities. The ABO objective grading system (OGS) and the IUSD comprehensive clinical assessment (CCA) were used to evaluate the clinical outcome for all patients. RESULTS: The average treatment duration was 29 months. The mean DI, OGS, and CCA scores were 15.30, 23.34, and 4.48, respectively. Increased treatment length was associated with 0.022-in slot size brackets, percent of treatment spent in nickel-titanium wires, Class II malocclusion, increased DI score, and increased TCI score. In evaluating outcomes for 2004 through 2006, there was no significant relationship between treatment duration and clinical outcome as measured by the OGS and CCA scores. CONCLUSIONS: The DI and TCI are sensitive prospective indicators of treatment duration. After the introduction of a rigorous clinical protocol for controlling poor outcomes, because of patients exceeding predicted treatment times, the clinical results for this sample are independent of treatment duration.


Asunto(s)
Educación de Posgrado en Odontología/métodos , Maloclusión/terapia , Ortodoncia Correctiva/normas , Ortodoncia/educación , Adolescente , Adulto , Análisis de Varianza , Niño , Competencia Clínica , Clínicas Odontológicas , Episodio de Atención , Femenino , Humanos , Masculino , Maloclusión/patología , Persona de Mediana Edad , Aparatos Ortodóncicos , Ortodoncia Correctiva/instrumentación , Ortodoncia Correctiva/métodos , Cooperación del Paciente , Análisis de Regresión , Escalas de Valor Relativo , Estudios Retrospectivos , Estadísticas no Paramétricas , Factores de Tiempo , Resultado del Tratamiento
17.
Am J Orthod Dentofacial Orthop ; 134(6): 742-50, 2008 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-19061800

RESUMEN

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.


Asunto(s)
Predisposición Genética a la Enfermedad/genética , Resorción Radicular/genética , Técnicas de Movimiento Dental/efectos adversos , Fosfatasa Ácida/análisis , Alelos , Animales , Biomarcadores/análisis , Cruzamientos Genéticos , Modelos Animales de Enfermedad , Femenino , Genes Dominantes/genética , Isoenzimas/análisis , Masculino , Ratones , Ratones Endogámicos A , Ratones Endogámicos BALB C , Ratones Endogámicos DBA , Ratones Endogámicos , Diente Molar/patología , Herencia Multifactorial/genética , Factores Sexuales , Estrés Mecánico , Fosfatasa Ácida Tartratorresistente
18.
Am J Orthod Dentofacial Orthop ; 133(6): 791.e11-26, 2008 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-18538239

RESUMEN

INTRODUCTION: The tension-compression theory of bone mechanotransduction is ubiquitous in orthodontics. However, partly due to deficiencies in the characterization of the mechanical environment, there is no consensus on the mechanisms that link stimuli to root resorption and bone response. In this study, we analyzed the predominant directions of tension and compression in the alveolar structures. METHODS: An idealized tooth model was constructed with computer-aided design for finite element stress analysis. The principal stress magnitudes and directions were calculated in tipping and translation. RESULTS: The highest principal stress magnitudes in the root, periodontal ligament (PDL), and alveolar surface occurred predominantly in the longitudinal, radial, and hoop directions, respectively. On the compression side, the only structure consistently in compression in all directions was the PDL; however, magnitudes were different in different directions. CONCLUSIONS: In the same region of root, PDL, and bone, there can be compression in 1 structure and tension in another. At a given point in a structure, compression and tension can coexist in different directions. Magnitudes of compression and tension are typically different in different directions. Because of direction swaps between principal stresses, previously published data of only stress magnitude plots can be confusing and perhaps impossible to understand or correlate with biological responses. To prevent ambiguities, a reference to a principal stress should include not only the structure, but also its predominant direction. Combined stress magnitude and direction results suggest that the PDL is the initiator of mechanotransduction.


Asunto(s)
Análisis del Estrés Dental/métodos , Ligamento Periodontal/fisiología , Resorción Radicular/etiología , Técnicas de Movimiento Dental/efectos adversos , Proceso Alveolar/fisiología , Fuerza Compresiva , Simulación por Computador , Diseño Asistido por Computadora , Diente Canino/fisiología , Análisis del Estrés Dental/instrumentación , Análisis de Elementos Finitos , Análisis Numérico Asistido por Computador , Estrés Mecánico , Resistencia a la Tracción , Raíz del Diente/fisiología
19.
Am J Orthod Dentofacial Orthop ; 132(6): 822-9, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18068603

RESUMEN

INTRODUCTION: The American Board of Orthodontics (ABO) discrepancy index (DI) quantifies the severity of a malocclusion. The ABO objective grading system (OGS) assesses the quality of orthodontic finishing. Indiana University's comprehensive clinical assessment (CCA) supplements the OGS to provide an instrument to determine clinical outcomes. The purposes of this article were to (1) determine whether treatment outcome is related to the type of malocclusion as defined by the ABO classification, (2) determine the fraction of finished orthodontic cases in the graduate orthodontics clinic that are within the ABO standards for passing the phase III clinical examination, (3) evaluate the contribution of each component of the OGS and the CCA to the total OGS and CCA scores, (4) determine the percentage of finished cases that meet the ABO case category specifications, and (5) identify problem areas to improve the quality of treatment for challenging malocclusions. METHODS: Three hundred eighty-two cases that satisfied requirements for 8 of the ABO's malocclusion categories were selected from 989 consecutively finished cases from 1998 through 2003. They were evaluated by using the OGS, the CCA, and the DI. RESULTS: The average OGS score was 32.64, the average CCA score was 5.62, and the average DI score was 20.94. There was no significant difference in the OGS and the CCA scores among the categories. Categories 2, 5, 7, and 8 had a DI score that was significantly higher than the average for the entire sample. The OGS and CCA scores were positively correlated with the DI score, meaning that complex malocclusions are challenging to finish well. The most points lost for the OGS and the CCA were for occlusal contacts and treatment efficiency (length of treatment relative to the result), respectively. The fewest points lost were for interproximal contacts and vertical control, respectively. Furthermore, prematurely terminated cases (early debonds) had longer treatment times and higher (worse) OGS and CCA scores. CONCLUSIONS: This study demonstrates problems in treating complex malocclusions in a graduate orthodontics program and suggests methods for increasing the quality of clinical outcomes.


Asunto(s)
Educación de Posgrado en Odontología/normas , Maloclusión/clasificación , Maloclusión/terapia , Ortodoncia Correctiva/normas , Ortodoncia/educación , Adolescente , Adulto , Análisis de Varianza , Niño , Clínicas Odontológicas/normas , Femenino , Humanos , Indiana , Modelos Logísticos , Masculino , Persona de Mediana Edad , Reproducibilidad de los Resultados , Estudios Retrospectivos , Índice de Severidad de la Enfermedad , Consejos de Especialidades , Estadísticas no Paramétricas , Resultado del Tratamiento
20.
Eur J Hum Genet ; 10(9): 516-20, 2002 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-12173028

RESUMEN

Nance-Horan syndrome (NHS) is an X-linked condition characterised by congenital cataracts, dental abnormalities, dysmorphic features, and mental retardation in some cases. Previous studies have mapped the disease gene to a 2 cM interval on Xp22.2 between DXS43 and DXS999. We report additional linkage data resulting from the analysis of eleven independent NHS families. A maximum lod score of 9.94 (theta=0.00) was obtained at the RS1 locus and a recombination with locus DXS1195 on the telomeric side was observed in two families, thus refining the location of the gene to an interval of around 1 Mb on Xp22.13. Direct sequencing or SSCP analysis of the coding exons of five genes (SCML1, SCML2, STK9, RS1 and PPEF1), considered as candidate genes on the basis of their location in the critical interval, failed to detect any mutation in 12 unrelated NHS patients, thus making it highly unlikely that these genes are implicated in NHS.


Asunto(s)
Catarata/genética , Cromosomas Humanos X , Anomalías Congénitas/genética , Polimorfismo Conformacional Retorcido-Simple , Catarata/congénito , Mapeo Cromosómico , Exones , Femenino , Ligamiento Genético , Marcadores Genéticos , Humanos , Discapacidad Intelectual/genética , Escala de Lod , Masculino , Linaje , Recombinación Genética , Síndrome
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