Literature DB >> 22560383

Contribution of Hla-B51 in the susceptibility and specific clinical features of Behcet's disease in Tunisian patients.

Amira Hamzaoui1, Mohamed Habib Houman, Meriem Massouadia, Thouraya Ben Salem, Monia Smiti Khanfir, Imed Ben Ghorbel, Mohamed Miled.   

Abstract

BACKGROUND: Many researchers have tried to investigate the association of HLA-B51 with the severity and the clinical features of BD with conflicting results.
METHODS: We aimed at investigating the association of HLA-B51 with demographical and clinical manifestations as well as the severity of BD, by studying 178 native Tunisian BD patients, fulfilling the International Study group criteria for the BD classification recruited from the Department of Internal Medicine, Rabta Hospital in Tunis and compared with 125 native Tunisian healthy age and sex matching volunteers.
RESULTS: According to our findings, the frequency of HLAB 51 was significantly higher in BD patients than in controls (p<0.001). Positive pathergy test (PPT) (p = 0.01) and retinal vasculitis (p = 0.045), were significantly more frequent in HLA B51(+) patients, while the frequency of arterial aneurysms (p = 0.009) and neurological involvement, especially the parenchymal involvement (p<0.001), were significantly and clearly higher in HLA B51(-) patients. The patients without HLA B51 had a significantly less severe disease (p = 0.001). Discussion/conclusion We conclude that HLA B51 is a predisposing marker for BD in our population as in most ethnic groups. It seems to be associated with a subgroup of BD patients characterized by a higher frequency of ocular involvement and PPT, but a lower frequency of arterial aneurysm and neurological involvement, and a less severe disease course.
Copyright © 2011 European Federation of Internal Medicine. Published by Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22560383     DOI: 10.1016/j.ejim.2011.12.011

Source DB:  PubMed          Journal:  Eur J Intern Med        ISSN: 0953-6205            Impact factor:   4.487


  8 in total

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2.  Past and Present Behçet's Disease Animal Models.

Authors:  Jermilia Charles; Francis J Castellino; Victoria A Ploplis
Journal:  Curr Drug Targets       Date:  2020       Impact factor: 3.465

3.  Influence of corticosteroid therapy on IL-18 and nitric oxide production during Behçet's disease.

Authors:  Fatmazohra Djaballah-Ider; Zineb Djeraba; Mourad Chemli; Nadjiba Dammene-Debbihe; Doulkifly Lounis; Houda Belguendouz; Yanis Medour; Samia Chaib; Chafia Touil-Boukoffa
Journal:  Inflammopharmacology       Date:  2018-03-29       Impact factor: 4.473

4.  Behçet disease, new insights in disease associations and manifestations: a next-generation sequencing study.

Authors:  M Elfishawi; G Mossallam; D G Augusto; G Montero-Martin; H de Bruin; L Van de Pasch; P J Norman; E Rozemuller; M Fernandez-Vina; A Abrudescu; J A Hollenbach; K Zaky; S Elfishawi
Journal:  Clin Exp Immunol       Date:  2021-02-03       Impact factor: 5.732

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Review 6.  Immune Regulatory Genes Are Major Genetic Factors to Behcet Disease: Systematic Review.

Authors:  Yan Deng; Weifeng Zhu; Xiaodong Zhou
Journal:  Open Rheumatol J       Date:  2018-06-29

7.  Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51.

Authors:  Hee Jung Ryu; Mi Ryoung Seo; Hyo Jin Choi; Han Joo Baek
Journal:  Korean J Intern Med       Date:  2017-01-12       Impact factor: 2.884

Review 8.  Current State of Precision Medicine in Primary Systemic Vasculitides.

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  8 in total

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