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Influence of gender on Behçet's disease phenotype and irreversible organ damage: Data from the International AIDA Network Behçet's Disease Registry

8Citations signalées, ce qui n’est pas une note de qualité
70Institutions déclarées
13Pays d’affiliation déclarés

Rattachement africain : it, Égypte, sa, tr, mx, br, gr, es, Tunisie, ro, pl, co, ir. Niveau de preuve : code pays fourni par la source.

Le résumé fourni par la source

OBJECTIVES: Gender impact on phenotypical expression of Behçet's disease (BD) has been specifically investigated only in a few large-scale studies. The main goal of the study was to examine gender differences in a large cohort of patients affected by BD. METHODS: Data were retrieved from the International AIDA Network Registry for BD. We assessed differences between males and females in terms of Behçet's syndrome Overall Damage Index (BODI), differences in the disease manifestations at onset and in the cumulative manifestations throughout disease course, as well as differences in the cardiovascular risk. Finally, predictive factors leading to major organ involvement were investigated. RESULTS: In total, 1024 BD patients (567 males, 457 females) were enrolled in the study, with a male-to-female ratio of 1.24/1. Males displayed a significantly higher mean±SD BODI (1.92±2.09) at the last follow-up, compared to female patients (1.25±1.87) (P<0.0001). Uveitis (P<0.0001) and vascular involvement (P=0.0076) were significantly more frequent among males whereas female patients were significantly over-represented in arthralgia (P<0.0001), arthritis (P=0.00025), isolated headache (P<0.0001), central nervous system (CNS) involvement (P=0.040), and gastrointestinal involvement (P=0.00046). Regarding cardiovascular risk, no differences between the two groups emerged (P=0.617). Four variables were associated with the development of major organ involvement: male gender (OR=2.104, P=0.001), current treatment with biologic agents (OR=2.257, P=0.0003), origin from endemic countries (OR=2.661, P=0.0009), and disease duration (OR=1.002, P=0.024). CONCLUSION: BD displays a more severe course among males. This subgroup develops more irreversible damage and presents more frequently ocular and vascular involvement during disease course. On the other hand, female patients are prone to experience articular involvement, headache, CNS and gastrointestinal involvement. These data suggest the existence of a gender-driven disease expression.

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Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Influence of gender on Behçet's disease phenotype and irreversible organ damage: Data from the International AIDA Network Behçet's Disease Registry
Date Crossref
01/03/2025
Éditeur
Elsevier BV
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Les institutions déclarées

University of SienaCairo UniversityOctober 6 UniversityNew Giza UniversityKing Saud UniversityUniversity of Bari Aldo MoroGazi UniversityMarmara UniversityInstituto Nacional de Ciencias Médicas y Nutrición Salvador ZubiránHospital das Clínicas da Faculdade de Medicina da Universidade de São PauloUniversity of Rome Tor VergataNational and Kapodistrian University of AthensUniversity of CagliariUniversity of L'AquilaUniversity of FerraraArcispedale Sant'AnnaUniversity of TurinSan Salvatore HospitalUniversitat de BarcelonaPoliclinico San Matteo FondazioneIstanbul University-CerrahpaşaUniversity of BresciaUniversità Campus Bio-MedicoMansoura UniversityHorus University – EgyptUniversity of SousseUniversity of Campania "Luigi Vanvitelli"Ospedale di CattinaraAzienda Ospedaliera Universitaria Integrata VeronaSivas Cumhuriyet ÜniversitesiOspedale generale di zona San Camillo TrevisoHacettepe UniversityCarol Davila University of Medicine and PharmacyIstituto Ortopedico Gaetano PiniASL RomaOspedale San PaoloCivitaAzienda Socio Sanitaria Territoriale degli Spedali Civili di BresciaUniversity of PerugiaManisa Celal Bayar UniversityAzienda Ospedaliera Universitaria Policlinico "G. Martino"Ospedale di BolzanoAzienda di Rilievo Nazionale ed Alta SpecializzazioneNuovo Ospedale San Giovanni di DioUniversity of FlorenceLuigi Sacco HospitalUniversity of Chieti-PescaraFederico II University HospitalUniversity of Naples Federico IIHospital Universitario Fundación Jiménez DíazOspedale Pediatrico Giovanni XXIIICentral Clinical HospitalUniversidad del RosarioShariati HospitalTehran University of Medical SciencesDepartment of HealthUniversity of PalermoOspedale Vincenzo CervelloUniversità Cattolica del Sacro CuoreAgostino Gemelli University PolyclinicDokuz Eylül UniversityAnkara Yıldırım Beyazıt UniversityBambino Gesù Children's HospitalSapienza University of RomeUniversity of CataniaFatebenefratelli HospitalOspedale GaribaldiASST Fatebenefratelli SaccoEvangelismos HospitalAzienda Ospedaliera Universitaria Senese

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

Ocular Diseases and Behçet’s SyndromeAutoimmune and Inflammatory Disorders ResearchOtitis Media and Relapsing Polychondritis

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