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A national cohort study on pediatric Behçet’s disease: cross-sectional data from an Italian registry
BACKGROUND: Behçet’s disease is a rare multi-systemic inflammatory disease with unknown etiology which involves principally oral and genital mucosa, skin and eyes. Average age at onset of the disease is about 25-30 years, but it may be diagnosed before the age of 16. It is not very rare in Italy, ev...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740899/ https://www.ncbi.nlm.nih.gov/pubmed/29268757 http://dx.doi.org/10.1186/s12969-017-0213-x |
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author | Gallizzi, Romina Pidone, Caterina Cantarini, Luca Finetti, Martina Cattalini, Marco Filocamo, Giovanni Insalaco, Antonella Rigante, Donato Consolini, Rita Maggio, Maria Cristina Civino, Adele Martino, Silvana Olivieri, Alma Nunzia Fabio, Giovanna Pastore, Serena Mauro, Angela Sutera, Diana Trimarchi, Giuseppe Ruperto, Nicolino Gattorno, Marco Cimaz, Rolando |
author_facet | Gallizzi, Romina Pidone, Caterina Cantarini, Luca Finetti, Martina Cattalini, Marco Filocamo, Giovanni Insalaco, Antonella Rigante, Donato Consolini, Rita Maggio, Maria Cristina Civino, Adele Martino, Silvana Olivieri, Alma Nunzia Fabio, Giovanna Pastore, Serena Mauro, Angela Sutera, Diana Trimarchi, Giuseppe Ruperto, Nicolino Gattorno, Marco Cimaz, Rolando |
author_sort | Gallizzi, Romina |
collection | PubMed |
description | BACKGROUND: Behçet’s disease is a rare multi-systemic inflammatory disease with unknown etiology which involves principally oral and genital mucosa, skin and eyes. Average age at onset of the disease is about 25-30 years, but it may be diagnosed before the age of 16. It is not very rare in Italy, even though there are limited data concerning epidemiology. Aim of this study is to describe the baseline data of an Italian cohort of patients with as having BD or probable BD. METHODS: We described the baseline data of the first national epidemiological study on children coming from 16 Italian Pediatric Rheumatologic Centers diagnosed by the treating physicians as having Behçet’s Disease. Data on demographic characteristics, clinical features and therapy were collected. We then compared our findings to those of international pediatric cohort studies and also retrospectively evaluated the ability to diagnose BD using ISG, ICBD and, for the first time, the new PEDBD criteria. RESULTS: The study included 110 patients (62 M, 48F). Average age at onset was 8.34±4.11 years. The frequencies of signs/symptoms were: recurrent oral aphtosis 94.5%, genital ulcers 33.6%, ocular 43.6%, gastrointestinal 42.7%, musculoskeletal 42.7%, neurological 30.9% and vascular involvement 10%. Thirty-two patients (29.1%) fulfilled ISG, 78 (70.9%) ICBD, 50 (45.5%) PEDBD criteria and 31 (28%) didn’t fulfill any of them. The most frequently used treatments were colchicine and corticosteroids followed by immunosuppressants. Four patients received biologic therapy (anti TNF-α and anti-IL-1) to treat severe organ involvement. CONCLUSIONS: Recurrent oral aphtosis was the most frequent clinical manifestation, followed by ocular involvement. Gastrointestinal lesions were more frequent in Italy than in non-European countries as opposed to genital ulcers. Skin, ocular and vascular manifestations had a higher frequency in males and genital ulcers in females. Constitutional symptoms were present in 44.5% and recurrent fever in one third of our population. |
format | Online Article Text |
id | pubmed-5740899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57408992018-01-03 A national cohort study on pediatric Behçet’s disease: cross-sectional data from an Italian registry Gallizzi, Romina Pidone, Caterina Cantarini, Luca Finetti, Martina Cattalini, Marco Filocamo, Giovanni Insalaco, Antonella Rigante, Donato Consolini, Rita Maggio, Maria Cristina Civino, Adele Martino, Silvana Olivieri, Alma Nunzia Fabio, Giovanna Pastore, Serena Mauro, Angela Sutera, Diana Trimarchi, Giuseppe Ruperto, Nicolino Gattorno, Marco Cimaz, Rolando Pediatr Rheumatol Online J Research Article BACKGROUND: Behçet’s disease is a rare multi-systemic inflammatory disease with unknown etiology which involves principally oral and genital mucosa, skin and eyes. Average age at onset of the disease is about 25-30 years, but it may be diagnosed before the age of 16. It is not very rare in Italy, even though there are limited data concerning epidemiology. Aim of this study is to describe the baseline data of an Italian cohort of patients with as having BD or probable BD. METHODS: We described the baseline data of the first national epidemiological study on children coming from 16 Italian Pediatric Rheumatologic Centers diagnosed by the treating physicians as having Behçet’s Disease. Data on demographic characteristics, clinical features and therapy were collected. We then compared our findings to those of international pediatric cohort studies and also retrospectively evaluated the ability to diagnose BD using ISG, ICBD and, for the first time, the new PEDBD criteria. RESULTS: The study included 110 patients (62 M, 48F). Average age at onset was 8.34±4.11 years. The frequencies of signs/symptoms were: recurrent oral aphtosis 94.5%, genital ulcers 33.6%, ocular 43.6%, gastrointestinal 42.7%, musculoskeletal 42.7%, neurological 30.9% and vascular involvement 10%. Thirty-two patients (29.1%) fulfilled ISG, 78 (70.9%) ICBD, 50 (45.5%) PEDBD criteria and 31 (28%) didn’t fulfill any of them. The most frequently used treatments were colchicine and corticosteroids followed by immunosuppressants. Four patients received biologic therapy (anti TNF-α and anti-IL-1) to treat severe organ involvement. CONCLUSIONS: Recurrent oral aphtosis was the most frequent clinical manifestation, followed by ocular involvement. Gastrointestinal lesions were more frequent in Italy than in non-European countries as opposed to genital ulcers. Skin, ocular and vascular manifestations had a higher frequency in males and genital ulcers in females. Constitutional symptoms were present in 44.5% and recurrent fever in one third of our population. BioMed Central 2017-12-21 /pmc/articles/PMC5740899/ /pubmed/29268757 http://dx.doi.org/10.1186/s12969-017-0213-x Text en © The Author(s). 2017 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Gallizzi, Romina Pidone, Caterina Cantarini, Luca Finetti, Martina Cattalini, Marco Filocamo, Giovanni Insalaco, Antonella Rigante, Donato Consolini, Rita Maggio, Maria Cristina Civino, Adele Martino, Silvana Olivieri, Alma Nunzia Fabio, Giovanna Pastore, Serena Mauro, Angela Sutera, Diana Trimarchi, Giuseppe Ruperto, Nicolino Gattorno, Marco Cimaz, Rolando A national cohort study on pediatric Behçet’s disease: cross-sectional data from an Italian registry |
title | A national cohort study on pediatric Behçet’s disease: cross-sectional data from an Italian registry |
title_full | A national cohort study on pediatric Behçet’s disease: cross-sectional data from an Italian registry |
title_fullStr | A national cohort study on pediatric Behçet’s disease: cross-sectional data from an Italian registry |
title_full_unstemmed | A national cohort study on pediatric Behçet’s disease: cross-sectional data from an Italian registry |
title_short | A national cohort study on pediatric Behçet’s disease: cross-sectional data from an Italian registry |
title_sort | national cohort study on pediatric behçet’s disease: cross-sectional data from an italian registry |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740899/ https://www.ncbi.nlm.nih.gov/pubmed/29268757 http://dx.doi.org/10.1186/s12969-017-0213-x |
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