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Dental manifestations in adult hypophosphatasia and their correlation with biomarkers

Hypophosphatasia (HPP) is a genetic condition with broad clinical manifestations caused by alkaline phosphatase (ALP) deficiency. Adults with HPP exhibit a wide spectrum of signs and symptoms. Dental manifestations including premature tooth loss are common. Much of the published literature reporting...

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Autores principales: Sinha, Priya, Gabor, Rachel, Haupt‐Harrington, Rachael, Deering, Leila, Steiner, Robert D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458606/
https://www.ncbi.nlm.nih.gov/pubmed/36101824
http://dx.doi.org/10.1002/jmd2.12307
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author Sinha, Priya
Gabor, Rachel
Haupt‐Harrington, Rachael
Deering, Leila
Steiner, Robert D.
author_facet Sinha, Priya
Gabor, Rachel
Haupt‐Harrington, Rachael
Deering, Leila
Steiner, Robert D.
author_sort Sinha, Priya
collection PubMed
description Hypophosphatasia (HPP) is a genetic condition with broad clinical manifestations caused by alkaline phosphatase (ALP) deficiency. Adults with HPP exhibit a wide spectrum of signs and symptoms. Dental manifestations including premature tooth loss are common. Much of the published literature reporting dental manifestations consists of case reports and series of symptomatic patients, likely biased towards more severe dental manifestations. The objective of this study was to systematically explore the dental manifestations among adults with HPP by conducting a comprehensive dental evaluation. To minimize bias, the study explored dental manifestations in an unselected cohort of adults with HPP. Participants were identified searching electronic health record (EHR) data from a rural health system to discover adults with persistent ALP deficiency. Heterozygotes with pathogenic (P), likely pathogenic (LP), or uncertain variants (VUS) in ALPL and at least one elevated ALP substrate were defined as adults with HPP and underwent genetic, dental, oral radiographic, and biomarker evaluation. Twenty‐seven participants completed the study. Premature tooth loss was present in 63% (17/27); 19% (5/27) were missing eight or more teeth. Statistically significant associations were found between premature permanent tooth loss and HPP biomarkers ALP (p = 0.049) and bone‐specific ALP (p = 0.006). Serum ALP (ρ = −0.43, p = 0.037) and bone‐specific ALP (ρ = −0.57, p = 0.004) were negatively correlated with number of teeth lost prematurely. As noted with tooth loss, periodontal breakdown was associated with bone‐specific ALP. An inverse association between periodontal breakdown and bone‐specific ALP was observed (p = 0.014). These findings suggest a role for ALP in maintenance of dentition.
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spelling pubmed-94586062022-09-12 Dental manifestations in adult hypophosphatasia and their correlation with biomarkers Sinha, Priya Gabor, Rachel Haupt‐Harrington, Rachael Deering, Leila Steiner, Robert D. JIMD Rep Research Reports Hypophosphatasia (HPP) is a genetic condition with broad clinical manifestations caused by alkaline phosphatase (ALP) deficiency. Adults with HPP exhibit a wide spectrum of signs and symptoms. Dental manifestations including premature tooth loss are common. Much of the published literature reporting dental manifestations consists of case reports and series of symptomatic patients, likely biased towards more severe dental manifestations. The objective of this study was to systematically explore the dental manifestations among adults with HPP by conducting a comprehensive dental evaluation. To minimize bias, the study explored dental manifestations in an unselected cohort of adults with HPP. Participants were identified searching electronic health record (EHR) data from a rural health system to discover adults with persistent ALP deficiency. Heterozygotes with pathogenic (P), likely pathogenic (LP), or uncertain variants (VUS) in ALPL and at least one elevated ALP substrate were defined as adults with HPP and underwent genetic, dental, oral radiographic, and biomarker evaluation. Twenty‐seven participants completed the study. Premature tooth loss was present in 63% (17/27); 19% (5/27) were missing eight or more teeth. Statistically significant associations were found between premature permanent tooth loss and HPP biomarkers ALP (p = 0.049) and bone‐specific ALP (p = 0.006). Serum ALP (ρ = −0.43, p = 0.037) and bone‐specific ALP (ρ = −0.57, p = 0.004) were negatively correlated with number of teeth lost prematurely. As noted with tooth loss, periodontal breakdown was associated with bone‐specific ALP. An inverse association between periodontal breakdown and bone‐specific ALP was observed (p = 0.014). These findings suggest a role for ALP in maintenance of dentition. John Wiley & Sons, Inc. 2022-06-28 /pmc/articles/PMC9458606/ /pubmed/36101824 http://dx.doi.org/10.1002/jmd2.12307 Text en © 2022 The Authors. JIMD Reports published by John Wiley & Sons Ltd on behalf of SSIEM. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Reports
Sinha, Priya
Gabor, Rachel
Haupt‐Harrington, Rachael
Deering, Leila
Steiner, Robert D.
Dental manifestations in adult hypophosphatasia and their correlation with biomarkers
title Dental manifestations in adult hypophosphatasia and their correlation with biomarkers
title_full Dental manifestations in adult hypophosphatasia and their correlation with biomarkers
title_fullStr Dental manifestations in adult hypophosphatasia and their correlation with biomarkers
title_full_unstemmed Dental manifestations in adult hypophosphatasia and their correlation with biomarkers
title_short Dental manifestations in adult hypophosphatasia and their correlation with biomarkers
title_sort dental manifestations in adult hypophosphatasia and their correlation with biomarkers
topic Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458606/
https://www.ncbi.nlm.nih.gov/pubmed/36101824
http://dx.doi.org/10.1002/jmd2.12307
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