Cargando…

A systematic review of primary Sjögren’s syndrome in male and paediatric populations

Primary Sjögren’s syndrome (pSS) is a chronic multisystem autoimmune rheumatic disease characterised by female predominance. Although the disease is rare in the male and paediatric populations, it has been suggested that it may have a different disease phenotype, which has not been investigated befo...

Descripción completa

Detalles Bibliográficos
Autores principales: Virdee, Simrun, Greenan-Barrett, James, Ciurtin, Coziana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596040/
https://www.ncbi.nlm.nih.gov/pubmed/28735431
http://dx.doi.org/10.1007/s10067-017-3745-z
_version_ 1783263468795723776
author Virdee, Simrun
Greenan-Barrett, James
Ciurtin, Coziana
author_facet Virdee, Simrun
Greenan-Barrett, James
Ciurtin, Coziana
author_sort Virdee, Simrun
collection PubMed
description Primary Sjögren’s syndrome (pSS) is a chronic multisystem autoimmune rheumatic disease characterised by female predominance. Although the disease is rare in the male and paediatric populations, it has been suggested that it may have a different disease phenotype, which has not been investigated before using a systematic approach. A systematic literature search of PubMed databases (updated to December 2016) was performed to identify all published data on the epidemiological, clinical and laboratory manifestations of pSS in the male and paediatric populations. The literature search of the male and paediatric pSS studies identified 2025 and 186 citations, respectively, out of which 7 and 5 fulfilled our inclusion criteria and were analysed further. The range of age at disease onset was 9.4–10.7 years for children and 39.4–56.9 years at diagnosis for male patients. We identified a prevalence of extra-glandular manifestations between 52.6–92.3% in the male population and 50.0–84.6% in children, while abnormal sialometry was only reported in the paediatric population, with a prevalence between 71.4 and 81.8%. There was a significant variation of positive serological markers, with anti-Ro antibodies reported between 15.7–75.0% and 36.4–84.6%, and anti-La antibodies between 5.6–51.7% and 27.3–65.4%, in the male and paediatric populations, respectively. The characteristics of pSS in the male and paediatric populations varied according to different studies. When compared to data available from pSS adult populations, children diagnosed with pSS reported less dryness and had a higher prevalence of parotitis, lymphadenopathy and systemic symptoms and male patients were younger at the time of diagnosis. This systematic review contributes to a better understanding of the epidemiology of pSS in rare populations. Large longitudinal cohort studies comparing male with female patients and adult with paediatric patients are needed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10067-017-3745-z) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5596040
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Springer London
record_format MEDLINE/PubMed
spelling pubmed-55960402017-09-26 A systematic review of primary Sjögren’s syndrome in male and paediatric populations Virdee, Simrun Greenan-Barrett, James Ciurtin, Coziana Clin Rheumatol Original Article Primary Sjögren’s syndrome (pSS) is a chronic multisystem autoimmune rheumatic disease characterised by female predominance. Although the disease is rare in the male and paediatric populations, it has been suggested that it may have a different disease phenotype, which has not been investigated before using a systematic approach. A systematic literature search of PubMed databases (updated to December 2016) was performed to identify all published data on the epidemiological, clinical and laboratory manifestations of pSS in the male and paediatric populations. The literature search of the male and paediatric pSS studies identified 2025 and 186 citations, respectively, out of which 7 and 5 fulfilled our inclusion criteria and were analysed further. The range of age at disease onset was 9.4–10.7 years for children and 39.4–56.9 years at diagnosis for male patients. We identified a prevalence of extra-glandular manifestations between 52.6–92.3% in the male population and 50.0–84.6% in children, while abnormal sialometry was only reported in the paediatric population, with a prevalence between 71.4 and 81.8%. There was a significant variation of positive serological markers, with anti-Ro antibodies reported between 15.7–75.0% and 36.4–84.6%, and anti-La antibodies between 5.6–51.7% and 27.3–65.4%, in the male and paediatric populations, respectively. The characteristics of pSS in the male and paediatric populations varied according to different studies. When compared to data available from pSS adult populations, children diagnosed with pSS reported less dryness and had a higher prevalence of parotitis, lymphadenopathy and systemic symptoms and male patients were younger at the time of diagnosis. This systematic review contributes to a better understanding of the epidemiology of pSS in rare populations. Large longitudinal cohort studies comparing male with female patients and adult with paediatric patients are needed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10067-017-3745-z) contains supplementary material, which is available to authorized users. Springer London 2017-07-22 2017 /pmc/articles/PMC5596040/ /pubmed/28735431 http://dx.doi.org/10.1007/s10067-017-3745-z Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Article
Virdee, Simrun
Greenan-Barrett, James
Ciurtin, Coziana
A systematic review of primary Sjögren’s syndrome in male and paediatric populations
title A systematic review of primary Sjögren’s syndrome in male and paediatric populations
title_full A systematic review of primary Sjögren’s syndrome in male and paediatric populations
title_fullStr A systematic review of primary Sjögren’s syndrome in male and paediatric populations
title_full_unstemmed A systematic review of primary Sjögren’s syndrome in male and paediatric populations
title_short A systematic review of primary Sjögren’s syndrome in male and paediatric populations
title_sort systematic review of primary sjögren’s syndrome in male and paediatric populations
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596040/
https://www.ncbi.nlm.nih.gov/pubmed/28735431
http://dx.doi.org/10.1007/s10067-017-3745-z
work_keys_str_mv AT virdeesimrun asystematicreviewofprimarysjogrenssyndromeinmaleandpaediatricpopulations
AT greenanbarrettjames asystematicreviewofprimarysjogrenssyndromeinmaleandpaediatricpopulations
AT ciurtincoziana asystematicreviewofprimarysjogrenssyndromeinmaleandpaediatricpopulations
AT virdeesimrun systematicreviewofprimarysjogrenssyndromeinmaleandpaediatricpopulations
AT greenanbarrettjames systematicreviewofprimarysjogrenssyndromeinmaleandpaediatricpopulations
AT ciurtincoziana systematicreviewofprimarysjogrenssyndromeinmaleandpaediatricpopulations