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Pathophysiology of Demineralization, Part II: Enamel White Spots, Cavitated Caries, and Bone Infection
PURPOSE OF REVIEW: Compare noninfectious (part I) to infectious (part II) demineralization of bones and teeth. Evaluate similarities and differences in the expression of hard tissue degradation for the two most common chronic demineralization diseases: osteoporosis and dental caries. RECENT FINDINGS...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930953/ https://www.ncbi.nlm.nih.gov/pubmed/35156182 http://dx.doi.org/10.1007/s11914-022-00723-0 |
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author | Roberts, W. Eugene Mangum, Jonathan E. Schneider, Paul M. |
author_facet | Roberts, W. Eugene Mangum, Jonathan E. Schneider, Paul M. |
author_sort | Roberts, W. Eugene |
collection | PubMed |
description | PURPOSE OF REVIEW: Compare noninfectious (part I) to infectious (part II) demineralization of bones and teeth. Evaluate similarities and differences in the expression of hard tissue degradation for the two most common chronic demineralization diseases: osteoporosis and dental caries. RECENT FINDINGS: The physiology of demineralization is similar for the sterile skeleton compared to the septic dentition. Superimposing the pathologic variable of infection reveals a unique pathophysiology for dental caries. SUMMARY: Mineralized tissues are compromised by microdamage, demineralization, and infection. Osseous tissues remodel (turnover) to maintain structural integrity, but the heavily loaded dentition does not turnover so it is ultimately at risk of collapse. A carious tooth is a potential vector for periapical infection that may be life-threatening. Insipient caries is initiated as a subsurface decalcification in enamel that is not detectable until a depth of ~400μm when it becomes visible as a white spot. Reliable detection and remineralization of invisible caries would advance cost-effective wellness worldwide. |
format | Online Article Text |
id | pubmed-8930953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-89309532022-04-01 Pathophysiology of Demineralization, Part II: Enamel White Spots, Cavitated Caries, and Bone Infection Roberts, W. Eugene Mangum, Jonathan E. Schneider, Paul M. Curr Osteoporos Rep Craniofacial Skeleton (TG Chu and S Akintoye, Section Editors) PURPOSE OF REVIEW: Compare noninfectious (part I) to infectious (part II) demineralization of bones and teeth. Evaluate similarities and differences in the expression of hard tissue degradation for the two most common chronic demineralization diseases: osteoporosis and dental caries. RECENT FINDINGS: The physiology of demineralization is similar for the sterile skeleton compared to the septic dentition. Superimposing the pathologic variable of infection reveals a unique pathophysiology for dental caries. SUMMARY: Mineralized tissues are compromised by microdamage, demineralization, and infection. Osseous tissues remodel (turnover) to maintain structural integrity, but the heavily loaded dentition does not turnover so it is ultimately at risk of collapse. A carious tooth is a potential vector for periapical infection that may be life-threatening. Insipient caries is initiated as a subsurface decalcification in enamel that is not detectable until a depth of ~400μm when it becomes visible as a white spot. Reliable detection and remineralization of invisible caries would advance cost-effective wellness worldwide. Springer US 2022-02-14 2022 /pmc/articles/PMC8930953/ /pubmed/35156182 http://dx.doi.org/10.1007/s11914-022-00723-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Craniofacial Skeleton (TG Chu and S Akintoye, Section Editors) Roberts, W. Eugene Mangum, Jonathan E. Schneider, Paul M. Pathophysiology of Demineralization, Part II: Enamel White Spots, Cavitated Caries, and Bone Infection |
title | Pathophysiology of Demineralization, Part II: Enamel White Spots, Cavitated Caries, and Bone Infection |
title_full | Pathophysiology of Demineralization, Part II: Enamel White Spots, Cavitated Caries, and Bone Infection |
title_fullStr | Pathophysiology of Demineralization, Part II: Enamel White Spots, Cavitated Caries, and Bone Infection |
title_full_unstemmed | Pathophysiology of Demineralization, Part II: Enamel White Spots, Cavitated Caries, and Bone Infection |
title_short | Pathophysiology of Demineralization, Part II: Enamel White Spots, Cavitated Caries, and Bone Infection |
title_sort | pathophysiology of demineralization, part ii: enamel white spots, cavitated caries, and bone infection |
topic | Craniofacial Skeleton (TG Chu and S Akintoye, Section Editors) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930953/ https://www.ncbi.nlm.nih.gov/pubmed/35156182 http://dx.doi.org/10.1007/s11914-022-00723-0 |
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