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Effect of self-assembling peptide P(11)-4 on orthodontic treatment-induced carious lesions

This study aimed to evaluate the effect of self-assembling peptide P(11)-4 (SAP) in the therapy of initial smooth surface caries (white spot lesions, WSL) following orthodontic multibracket treatment. Twenty-three patients (13f/10m; average age 15.4 years) with at least two teeth with WSL were recru...

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Autores principales: Welk, A., Ratzmann, A., Reich, M., Krey, K. F., Schwahn, Ch.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176635/
https://www.ncbi.nlm.nih.gov/pubmed/32321955
http://dx.doi.org/10.1038/s41598-020-63633-0
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author Welk, A.
Ratzmann, A.
Reich, M.
Krey, K. F.
Schwahn, Ch.
author_facet Welk, A.
Ratzmann, A.
Reich, M.
Krey, K. F.
Schwahn, Ch.
author_sort Welk, A.
collection PubMed
description This study aimed to evaluate the effect of self-assembling peptide P(11)-4 (SAP) in the therapy of initial smooth surface caries (white spot lesions, WSL) following orthodontic multibracket treatment. Twenty-three patients (13f/10m; average age 15.4 years) with at least two teeth with WSL were recruited for the randomised controlled clinical trial with split-mouth design. In opposite to the control teeth, the test teeth were treated with SAP on Day 0. The primary endpoint was the impedance measurement of WSL using customised tray to ensure reproducibility of the measurement location. The secondary endpoint was the morphometric measurement of WSL using a semi-automated approach to determine the WSL size in mm(2). Treatment effects were adjusted for site-specific baseline values using mixed models adapted from the cross-over design. Test WSL showed a mean baseline impedance value of 46.7, which decreased to 21.1, 18.4, and 19.7 after 45, 90, and 180 days, respectively. Control WSL showed a mean baseline value of 42.0, which decreased to 35.0, 29.5, and 33.7, respectively. The overall treatment contrast was −13.7 (95% CI: −19.6 – −7.7; p < 0.001). For the secondary endpoint, the test WSL size decreased from 8.8 at baseline to 6.5 after 180 days. The control WSL decreased from 6.8 to 5.7, respectively. The related treatment contrast was −1.0 in favour of test WSL (95% CI: −1.6 – −0.5; p = 0.004). The treatment of initial carious lesions with self-assembling peptide P(11)−4 leads to superior remineralisation of the subsurface lesions compared with the control teeth.
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spelling pubmed-71766352020-04-27 Effect of self-assembling peptide P(11)-4 on orthodontic treatment-induced carious lesions Welk, A. Ratzmann, A. Reich, M. Krey, K. F. Schwahn, Ch. Sci Rep Article This study aimed to evaluate the effect of self-assembling peptide P(11)-4 (SAP) in the therapy of initial smooth surface caries (white spot lesions, WSL) following orthodontic multibracket treatment. Twenty-three patients (13f/10m; average age 15.4 years) with at least two teeth with WSL were recruited for the randomised controlled clinical trial with split-mouth design. In opposite to the control teeth, the test teeth were treated with SAP on Day 0. The primary endpoint was the impedance measurement of WSL using customised tray to ensure reproducibility of the measurement location. The secondary endpoint was the morphometric measurement of WSL using a semi-automated approach to determine the WSL size in mm(2). Treatment effects were adjusted for site-specific baseline values using mixed models adapted from the cross-over design. Test WSL showed a mean baseline impedance value of 46.7, which decreased to 21.1, 18.4, and 19.7 after 45, 90, and 180 days, respectively. Control WSL showed a mean baseline value of 42.0, which decreased to 35.0, 29.5, and 33.7, respectively. The overall treatment contrast was −13.7 (95% CI: −19.6 – −7.7; p < 0.001). For the secondary endpoint, the test WSL size decreased from 8.8 at baseline to 6.5 after 180 days. The control WSL decreased from 6.8 to 5.7, respectively. The related treatment contrast was −1.0 in favour of test WSL (95% CI: −1.6 – −0.5; p = 0.004). The treatment of initial carious lesions with self-assembling peptide P(11)−4 leads to superior remineralisation of the subsurface lesions compared with the control teeth. Nature Publishing Group UK 2020-04-22 /pmc/articles/PMC7176635/ /pubmed/32321955 http://dx.doi.org/10.1038/s41598-020-63633-0 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Welk, A.
Ratzmann, A.
Reich, M.
Krey, K. F.
Schwahn, Ch.
Effect of self-assembling peptide P(11)-4 on orthodontic treatment-induced carious lesions
title Effect of self-assembling peptide P(11)-4 on orthodontic treatment-induced carious lesions
title_full Effect of self-assembling peptide P(11)-4 on orthodontic treatment-induced carious lesions
title_fullStr Effect of self-assembling peptide P(11)-4 on orthodontic treatment-induced carious lesions
title_full_unstemmed Effect of self-assembling peptide P(11)-4 on orthodontic treatment-induced carious lesions
title_short Effect of self-assembling peptide P(11)-4 on orthodontic treatment-induced carious lesions
title_sort effect of self-assembling peptide p(11)-4 on orthodontic treatment-induced carious lesions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176635/
https://www.ncbi.nlm.nih.gov/pubmed/32321955
http://dx.doi.org/10.1038/s41598-020-63633-0
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