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Comparison of salivary cytokines levels among individuals with Down syndrome, cerebral palsy and normoactive

BACKGROUND: Individuals with Down syndrome (DS) present increased susceptibility to infections and high prevalence of periodontal disease. The objective of this study is to evaluate the salivary concentrations of IL-1β, IL-6, IL-8, IL-10, TNFα and IL-12p70 of DS individuals and compare to cerebral p...

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Autores principales: Habibe, Carolina-Hartung, Yoshida, Rosemeire-Arai, Gorjão, Renata, de Gutierrez, Gabriela-Mancia, Heller, Debora, Birbrair, Alexander, Santos, Maria-Teresa-Botti-Rodrigues
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263772/
https://www.ncbi.nlm.nih.gov/pubmed/32509226
http://dx.doi.org/10.4317/jced.56336
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author Habibe, Carolina-Hartung
Yoshida, Rosemeire-Arai
Gorjão, Renata
de Gutierrez, Gabriela-Mancia
Heller, Debora
Birbrair, Alexander
Santos, Maria-Teresa-Botti-Rodrigues
author_facet Habibe, Carolina-Hartung
Yoshida, Rosemeire-Arai
Gorjão, Renata
de Gutierrez, Gabriela-Mancia
Heller, Debora
Birbrair, Alexander
Santos, Maria-Teresa-Botti-Rodrigues
author_sort Habibe, Carolina-Hartung
collection PubMed
description BACKGROUND: Individuals with Down syndrome (DS) present increased susceptibility to infections and high prevalence of periodontal disease. The objective of this study is to evaluate the salivary concentrations of IL-1β, IL-6, IL-8, IL-10, TNFα and IL-12p70 of DS individuals and compare to cerebral palsy (CP) and normoactive patients (all with gingivitis). MATERIAL AND METHODS: Twenty-two individuals with DS, 24 with CP and 22 normoactive participated in this cross-sectional study. Salivary flow rate, osmolality rate, Oral Hygiene Index, Gingival Index (GI) and salivary inflammatory markers IL-1β, IL-6, IL-8, IL-10, TNFα and IL-12p70 were evaluated. Shapiro-Wilks, Chi-square, ANOVA One-Way and Kruskal Wallis tests were applied with significance level at 5%. RESULTS: The groups were homogenous for gender, age, and IL12p70 cytokine (p>0.05). GI was significantly higher in DS compared to CP and healthy (p<0.05). CP presented reduced salivary flow and increased osmolality rate. CP showed significantly higher values for TNFα, IL10, and IL6 compared to DS and normoactive (p<0.05). DS and CP presented significantly higher values of IL-1β and IL8 compared to normoactive (p<0.05). CONCLUSIONS: Individuals with CP have higher risk to develop periodontal disease due to reduced salivary flow rate, increased salivary osmolality rate and elevated TNFα, IL-10, IL-6 compared to DS. Key words:Cytokines, biomarkers, gingivitis, periodontal diseases, Down syndrome, cerebral palsy, saliva.
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spelling pubmed-72637722020-06-04 Comparison of salivary cytokines levels among individuals with Down syndrome, cerebral palsy and normoactive Habibe, Carolina-Hartung Yoshida, Rosemeire-Arai Gorjão, Renata de Gutierrez, Gabriela-Mancia Heller, Debora Birbrair, Alexander Santos, Maria-Teresa-Botti-Rodrigues J Clin Exp Dent Research BACKGROUND: Individuals with Down syndrome (DS) present increased susceptibility to infections and high prevalence of periodontal disease. The objective of this study is to evaluate the salivary concentrations of IL-1β, IL-6, IL-8, IL-10, TNFα and IL-12p70 of DS individuals and compare to cerebral palsy (CP) and normoactive patients (all with gingivitis). MATERIAL AND METHODS: Twenty-two individuals with DS, 24 with CP and 22 normoactive participated in this cross-sectional study. Salivary flow rate, osmolality rate, Oral Hygiene Index, Gingival Index (GI) and salivary inflammatory markers IL-1β, IL-6, IL-8, IL-10, TNFα and IL-12p70 were evaluated. Shapiro-Wilks, Chi-square, ANOVA One-Way and Kruskal Wallis tests were applied with significance level at 5%. RESULTS: The groups were homogenous for gender, age, and IL12p70 cytokine (p>0.05). GI was significantly higher in DS compared to CP and healthy (p<0.05). CP presented reduced salivary flow and increased osmolality rate. CP showed significantly higher values for TNFα, IL10, and IL6 compared to DS and normoactive (p<0.05). DS and CP presented significantly higher values of IL-1β and IL8 compared to normoactive (p<0.05). CONCLUSIONS: Individuals with CP have higher risk to develop periodontal disease due to reduced salivary flow rate, increased salivary osmolality rate and elevated TNFα, IL-10, IL-6 compared to DS. Key words:Cytokines, biomarkers, gingivitis, periodontal diseases, Down syndrome, cerebral palsy, saliva. Medicina Oral S.L. 2020-05-01 /pmc/articles/PMC7263772/ /pubmed/32509226 http://dx.doi.org/10.4317/jced.56336 Text en Copyright: © 2020 Medicina Oral S.L. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Habibe, Carolina-Hartung
Yoshida, Rosemeire-Arai
Gorjão, Renata
de Gutierrez, Gabriela-Mancia
Heller, Debora
Birbrair, Alexander
Santos, Maria-Teresa-Botti-Rodrigues
Comparison of salivary cytokines levels among individuals with Down syndrome, cerebral palsy and normoactive
title Comparison of salivary cytokines levels among individuals with Down syndrome, cerebral palsy and normoactive
title_full Comparison of salivary cytokines levels among individuals with Down syndrome, cerebral palsy and normoactive
title_fullStr Comparison of salivary cytokines levels among individuals with Down syndrome, cerebral palsy and normoactive
title_full_unstemmed Comparison of salivary cytokines levels among individuals with Down syndrome, cerebral palsy and normoactive
title_short Comparison of salivary cytokines levels among individuals with Down syndrome, cerebral palsy and normoactive
title_sort comparison of salivary cytokines levels among individuals with down syndrome, cerebral palsy and normoactive
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263772/
https://www.ncbi.nlm.nih.gov/pubmed/32509226
http://dx.doi.org/10.4317/jced.56336
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