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Salivary microbiota and inflammation‐related proteins in patients with psoriasis

OBJECTIVE: The purpose of the present study was to characterize the composition of the salivary microbiota and quantify salivary levels of inflammation‐related proteins (neutrophil gelatinase‐associated lipocalin [NGAL] and transferrin) in patients with psoriasis and compare data to those obtained i...

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Detalles Bibliográficos
Autores principales: Belstrøm, Daniel, Eiberg, Josefine Maria, Enevold, Christian, Grande, Maria Anastasia, Jensen, Claus Antonio Juel, Skov, Lone, Hansen, Peter Riis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188313/
https://www.ncbi.nlm.nih.gov/pubmed/31916654
http://dx.doi.org/10.1111/odi.13277
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author Belstrøm, Daniel
Eiberg, Josefine Maria
Enevold, Christian
Grande, Maria Anastasia
Jensen, Claus Antonio Juel
Skov, Lone
Hansen, Peter Riis
author_facet Belstrøm, Daniel
Eiberg, Josefine Maria
Enevold, Christian
Grande, Maria Anastasia
Jensen, Claus Antonio Juel
Skov, Lone
Hansen, Peter Riis
author_sort Belstrøm, Daniel
collection PubMed
description OBJECTIVE: The purpose of the present study was to characterize the composition of the salivary microbiota and quantify salivary levels of inflammation‐related proteins (neutrophil gelatinase‐associated lipocalin [NGAL] and transferrin) in patients with psoriasis and compare data to those obtained in patients with periodontitis and orally healthy controls, respectively. MATERIALS AND METHODS: Stimulated saliva samples from patients with psoriasis (n = 27), patients with periodontitis (n = 58), and orally healthy controls (n = 52) were characterized by means of next‐generation sequencing of the 16S rRNA gene. Salivary levels of NGAL and transferrin were quantified using immunoassays. RESULTS: Linear discriminant effect size analysis showed that 52 (22 psoriasis‐associated and 30 periodontitis‐associated) and 21 (8 psoriasis‐associated and 13 orally healthy control‐associated) bacterial taxa differentiated the salivary microbiota in patients with psoriasis from that of patients with periodontitis and orally healthy controls, respectively. Significantly lower mean salivary levels of NGAL (psoriasis: 996 [std. error 320], periodontitis: 2,072 [295], orally healthy controls: 2,551 [345] ng/ml, p < .0001) and transferrin (psoriasis: 4.37 [0.92], periodontitis: 7.25 [0.88], orally healthy controls: 10.02 [0.94] ng/ml, p < .0001) were identified in patients with psoriasis. CONCLUSIONS: Psoriasis associates with characteristics of the salivary microbiota and salivary levels of inflammation‐related proteins, which are different from characteristics in patients with periodontitis and orally healthy controls, respectively.
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spelling pubmed-71883132020-04-29 Salivary microbiota and inflammation‐related proteins in patients with psoriasis Belstrøm, Daniel Eiberg, Josefine Maria Enevold, Christian Grande, Maria Anastasia Jensen, Claus Antonio Juel Skov, Lone Hansen, Peter Riis Oral Dis Oral and Systemic Health OBJECTIVE: The purpose of the present study was to characterize the composition of the salivary microbiota and quantify salivary levels of inflammation‐related proteins (neutrophil gelatinase‐associated lipocalin [NGAL] and transferrin) in patients with psoriasis and compare data to those obtained in patients with periodontitis and orally healthy controls, respectively. MATERIALS AND METHODS: Stimulated saliva samples from patients with psoriasis (n = 27), patients with periodontitis (n = 58), and orally healthy controls (n = 52) were characterized by means of next‐generation sequencing of the 16S rRNA gene. Salivary levels of NGAL and transferrin were quantified using immunoassays. RESULTS: Linear discriminant effect size analysis showed that 52 (22 psoriasis‐associated and 30 periodontitis‐associated) and 21 (8 psoriasis‐associated and 13 orally healthy control‐associated) bacterial taxa differentiated the salivary microbiota in patients with psoriasis from that of patients with periodontitis and orally healthy controls, respectively. Significantly lower mean salivary levels of NGAL (psoriasis: 996 [std. error 320], periodontitis: 2,072 [295], orally healthy controls: 2,551 [345] ng/ml, p < .0001) and transferrin (psoriasis: 4.37 [0.92], periodontitis: 7.25 [0.88], orally healthy controls: 10.02 [0.94] ng/ml, p < .0001) were identified in patients with psoriasis. CONCLUSIONS: Psoriasis associates with characteristics of the salivary microbiota and salivary levels of inflammation‐related proteins, which are different from characteristics in patients with periodontitis and orally healthy controls, respectively. John Wiley and Sons Inc. 2020-01-28 2020-04 /pmc/articles/PMC7188313/ /pubmed/31916654 http://dx.doi.org/10.1111/odi.13277 Text en © 2020 The Authors. Oral Diseases published by John Wiley & Sons Ltd. All rights reserved This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Oral and Systemic Health
Belstrøm, Daniel
Eiberg, Josefine Maria
Enevold, Christian
Grande, Maria Anastasia
Jensen, Claus Antonio Juel
Skov, Lone
Hansen, Peter Riis
Salivary microbiota and inflammation‐related proteins in patients with psoriasis
title Salivary microbiota and inflammation‐related proteins in patients with psoriasis
title_full Salivary microbiota and inflammation‐related proteins in patients with psoriasis
title_fullStr Salivary microbiota and inflammation‐related proteins in patients with psoriasis
title_full_unstemmed Salivary microbiota and inflammation‐related proteins in patients with psoriasis
title_short Salivary microbiota and inflammation‐related proteins in patients with psoriasis
title_sort salivary microbiota and inflammation‐related proteins in patients with psoriasis
topic Oral and Systemic Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188313/
https://www.ncbi.nlm.nih.gov/pubmed/31916654
http://dx.doi.org/10.1111/odi.13277
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