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Reliability of Beta angle in assessing true anteroposterior apical base discrepancy in different growth patterns
INTRODUCTION: Beta angle as a skeletal anteroposterior dysplasia indicator is known to be useful in evaluating normodivergent growth patterns. Hence, we compared and verified the accuracy of Beta angle in predicting sagittal jaw discrepancy among subjects with hyperdivergent, hypodivergent and normo...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367023/ https://www.ncbi.nlm.nih.gov/pubmed/25810649 http://dx.doi.org/10.4103/0976-9668.149109 |
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author | Sundareswaran, Shobha Kumar, Vinay |
author_facet | Sundareswaran, Shobha Kumar, Vinay |
author_sort | Sundareswaran, Shobha |
collection | PubMed |
description | INTRODUCTION: Beta angle as a skeletal anteroposterior dysplasia indicator is known to be useful in evaluating normodivergent growth patterns. Hence, we compared and verified the accuracy of Beta angle in predicting sagittal jaw discrepancy among subjects with hyperdivergent, hypodivergent and normodivergent growth patterns. MATERIALS AND METHODS: Lateral cephalometric radiographs of 179 patients belonging to skeletal Classes I, II, and III were further divided into normodivergent, hyperdivergent, and hypodivergent groups based on their vertical growth patterns. Sagittal dysplasia indicators - angle ANB, Wits appraisal, and Beta angle values were measured and tabulated. The perpendicular point of intersection on line CB (Condylion-Point B) in Beta angle was designated as ‘X’ and linear dimension XB was evaluated. RESULTS: Statistically significant increase was observed in the mean values of Beta angle and XB distance in the vertical growth pattern groups of both skeletal Class I and Class II patients thus pushing them toward Class III and Class I, respectively. CONCLUSIONS: Beta angle is a reliable indicator of sagittal dysplasia in normal and horizontal patterns of growth. However, vertical growth patterns significantly increased Beta angle values, thus affecting their reliability as a sagittal discrepancy assessment tool. Hence, Beta angle may not be a valid tool for assessment of sagittal jaw discrepancy in patients exhibiting vertical growth patterns with skeletal Class I and Class II malocclusions. Nevertheless, Class III malocclusions having the highest Beta angle values were unaffected. |
format | Online Article Text |
id | pubmed-4367023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43670232015-03-25 Reliability of Beta angle in assessing true anteroposterior apical base discrepancy in different growth patterns Sundareswaran, Shobha Kumar, Vinay J Nat Sci Biol Med Research Article INTRODUCTION: Beta angle as a skeletal anteroposterior dysplasia indicator is known to be useful in evaluating normodivergent growth patterns. Hence, we compared and verified the accuracy of Beta angle in predicting sagittal jaw discrepancy among subjects with hyperdivergent, hypodivergent and normodivergent growth patterns. MATERIALS AND METHODS: Lateral cephalometric radiographs of 179 patients belonging to skeletal Classes I, II, and III were further divided into normodivergent, hyperdivergent, and hypodivergent groups based on their vertical growth patterns. Sagittal dysplasia indicators - angle ANB, Wits appraisal, and Beta angle values were measured and tabulated. The perpendicular point of intersection on line CB (Condylion-Point B) in Beta angle was designated as ‘X’ and linear dimension XB was evaluated. RESULTS: Statistically significant increase was observed in the mean values of Beta angle and XB distance in the vertical growth pattern groups of both skeletal Class I and Class II patients thus pushing them toward Class III and Class I, respectively. CONCLUSIONS: Beta angle is a reliable indicator of sagittal dysplasia in normal and horizontal patterns of growth. However, vertical growth patterns significantly increased Beta angle values, thus affecting their reliability as a sagittal discrepancy assessment tool. Hence, Beta angle may not be a valid tool for assessment of sagittal jaw discrepancy in patients exhibiting vertical growth patterns with skeletal Class I and Class II malocclusions. Nevertheless, Class III malocclusions having the highest Beta angle values were unaffected. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4367023/ /pubmed/25810649 http://dx.doi.org/10.4103/0976-9668.149109 Text en Copyright: © Journal of Natural Science, Biology and Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sundareswaran, Shobha Kumar, Vinay Reliability of Beta angle in assessing true anteroposterior apical base discrepancy in different growth patterns |
title | Reliability of Beta angle in assessing true anteroposterior apical base discrepancy in different growth patterns |
title_full | Reliability of Beta angle in assessing true anteroposterior apical base discrepancy in different growth patterns |
title_fullStr | Reliability of Beta angle in assessing true anteroposterior apical base discrepancy in different growth patterns |
title_full_unstemmed | Reliability of Beta angle in assessing true anteroposterior apical base discrepancy in different growth patterns |
title_short | Reliability of Beta angle in assessing true anteroposterior apical base discrepancy in different growth patterns |
title_sort | reliability of beta angle in assessing true anteroposterior apical base discrepancy in different growth patterns |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367023/ https://www.ncbi.nlm.nih.gov/pubmed/25810649 http://dx.doi.org/10.4103/0976-9668.149109 |
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