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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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.
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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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