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Oral lesions in Sjögren’s syndrome: A systematic review
BACKGROUND: Sjögren’s syndrome (SS) is an autoimmune disease related to two common symptoms: dry mouth and eyes. Although, xerostomia and hyposialia have been frequently reported in these patients, not many studies have evaluated other oral manifestations. The aim of this systematic review was to in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medicina Oral S.L.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051685/ https://www.ncbi.nlm.nih.gov/pubmed/29924754 http://dx.doi.org/10.4317/medoral.22286 |
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author | Serrano, Julia López-Pintor, Rosa-María González-Serrano, José Fernández-Castro, Mónica Casañas, Elisabeth Hernández, Gonzalo |
author_facet | Serrano, Julia López-Pintor, Rosa-María González-Serrano, José Fernández-Castro, Mónica Casañas, Elisabeth Hernández, Gonzalo |
author_sort | Serrano, Julia |
collection | PubMed |
description | BACKGROUND: Sjögren’s syndrome (SS) is an autoimmune disease related to two common symptoms: dry mouth and eyes. Although, xerostomia and hyposialia have been frequently reported in these patients, not many studies have evaluated other oral manifestations. The aim of this systematic review was to investigate prevalence rates of oral lesions (OL) in SS patients and to compare it to a control group (CG), when available. MATERIAL AND METHODS: An exhaustive search of the published literature of the Pubmed, Scopus, Web of Science and the Cochrane Library databases was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols (PRISMA-P) for relevant studies that met our eligibility criteria (up to September 1st 2017). RESULTS: Seventeen cross-sectional studies and one cohort study were finally included. The results showed that SS patients presented more OL compared to non-SS patients. The most frequent types of OL registered in primary and secondary SS were angular cheilitis, atrophic glossitis, recurrent oral ulcerations and grooves or fissurations of the tongue, also when compared to a CG. CONCLUSIONS: OL are common and more frequent in SS patients when compared to a CG. This may be a consequence of low levels of saliva. More studies where these OL and all the possible cofounding factors are taken into account are needed. Key words:Sjögren’s syndrome, oral lesions, oral diseases, oral manifestations, oral disorders, systematic review. |
format | Online Article Text |
id | pubmed-6051685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medicina Oral S.L. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60516852018-07-23 Oral lesions in Sjögren’s syndrome: A systematic review Serrano, Julia López-Pintor, Rosa-María González-Serrano, José Fernández-Castro, Mónica Casañas, Elisabeth Hernández, Gonzalo Med Oral Patol Oral Cir Bucal Review BACKGROUND: Sjögren’s syndrome (SS) is an autoimmune disease related to two common symptoms: dry mouth and eyes. Although, xerostomia and hyposialia have been frequently reported in these patients, not many studies have evaluated other oral manifestations. The aim of this systematic review was to investigate prevalence rates of oral lesions (OL) in SS patients and to compare it to a control group (CG), when available. MATERIAL AND METHODS: An exhaustive search of the published literature of the Pubmed, Scopus, Web of Science and the Cochrane Library databases was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols (PRISMA-P) for relevant studies that met our eligibility criteria (up to September 1st 2017). RESULTS: Seventeen cross-sectional studies and one cohort study were finally included. The results showed that SS patients presented more OL compared to non-SS patients. The most frequent types of OL registered in primary and secondary SS were angular cheilitis, atrophic glossitis, recurrent oral ulcerations and grooves or fissurations of the tongue, also when compared to a CG. CONCLUSIONS: OL are common and more frequent in SS patients when compared to a CG. This may be a consequence of low levels of saliva. More studies where these OL and all the possible cofounding factors are taken into account are needed. Key words:Sjögren’s syndrome, oral lesions, oral diseases, oral manifestations, oral disorders, systematic review. Medicina Oral S.L. 2018-07 2018-06-21 /pmc/articles/PMC6051685/ /pubmed/29924754 http://dx.doi.org/10.4317/medoral.22286 Text en Copyright: © 2018 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 | Review Serrano, Julia López-Pintor, Rosa-María González-Serrano, José Fernández-Castro, Mónica Casañas, Elisabeth Hernández, Gonzalo Oral lesions in Sjögren’s syndrome: A systematic review |
title | Oral lesions in Sjögren’s syndrome: A systematic review |
title_full | Oral lesions in Sjögren’s syndrome: A systematic review |
title_fullStr | Oral lesions in Sjögren’s syndrome: A systematic review |
title_full_unstemmed | Oral lesions in Sjögren’s syndrome: A systematic review |
title_short | Oral lesions in Sjögren’s syndrome: A systematic review |
title_sort | oral lesions in sjögren’s syndrome: a systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051685/ https://www.ncbi.nlm.nih.gov/pubmed/29924754 http://dx.doi.org/10.4317/medoral.22286 |
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