Literature DB >> 15967189

Current concepts in the etiology and treatment of Behçet disease.

Cem Evereklioglu1.   

Abstract

Behçet disease is an idiopathic, multisystem, chronic, and recurrent disease characterized by exacerbations alternating with phases of quiescence, episodic panuveitis, and aggressive non-granulomatous occlusive vasculitis of the arteries and veins of any size with explosive ocular inflammatory attacks that primarily affect the retinal and anterior segment vasculature of the eye. The disease is characterized by endothelial dysfunction and may produce a wide variety of symptoms. In mild cases, orogenital ulcers and skin lesions are the only findings during the entire clinical course, whereas ocular lesions that occur in more than half of the cases, frequently bilateral, can eventually lead to blindness. Pulmonary, gastrointestinal, and central nervous system involvements may sometimes be life-threatening. This review examines the epidemiology, frequency, immunology, and immunohistopathology of Behçet disease with recent theories of several agents, including phosphoantigens, superantigens, heat-shock proteins, and adenosine deaminase. Perspectives on the possible roles of new etiopathological molecules, such as nitric oxide, endothelin, and homocysteine, are presented. Ocular and systemic clinical features, diagnostic criteria, classifications, laboratory, fundus fluorescein angiography, and radiologic imaging are discussed. Differential diagnosis, disease in pregnancy and childhood, and prognosis with regard to Behçet-induced systemic and ocular complications are also evaluated. Traditional and current treatments with topical, paraocular and systemic corticosteroids, colchicine, dapsone, cyclosporine, azathioprine, methotrexate, cyclophosphamide and chlorambucil are summarized and recent insights into the pharmacology and effects of thalidomide, tacrolimus (FK-506), interferon-alpha, anti-TNF-alpha blocking monoclonal autoantibody (infliximab) and soluble TNF receptor (etanercept) are reviewed. Key clinical investigations with the status of ongoing clinical trials aimed at addressing the drug's efficacy, surgical care, and studies that have raised the possibility of new therapeutic uses are also presented. The challenges posed by the drug's teratogenicity and adverse effects are also considered, if present.

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Year:  2005        PMID: 15967189     DOI: 10.1016/j.survophthal.2005.04.009

Source DB:  PubMed          Journal:  Surv Ophthalmol        ISSN: 0039-6257            Impact factor:   6.048


  88 in total

1.  Late-onset Behçet's disease: demographic, clinical, and ocular features.

Authors:  Gulten Sungur; Dicle Hazirolan; Emre Hekimoglu; Remzi Kasim; Sunay Duman
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2010-05-07       Impact factor: 3.117

2.  5,10-Methylenetetrahydrofolate reductase C677T gene polymorphism in Behcet's patients with or without ocular involvement.

Authors:  Y Ozkul; C Evereklioglu; M Borlu; S Taheri; M Calis; M Dündar; O Ilhan
Journal:  Br J Ophthalmol       Date:  2005-12       Impact factor: 4.638

3.  Adalimumab: a new modality for Behçet's disease?

Authors:  J A M van Laar; T Missotten; P L A van Daele; A Jamnitski; G S Baarsma; P M van Hagen
Journal:  Ann Rheum Dis       Date:  2006-11-23       Impact factor: 19.103

4.  Diagnostic dilemma between intestinal Behçet disease and inflammatory bowel disease with pyoderma gangrenosum.

Authors:  Cem Evereklioglu
Journal:  World J Gastroenterol       Date:  2006-09-21       Impact factor: 5.742

5.  Ocular manifestations of Behçet's disease in Jordanian patients.

Authors:  Mohammed A Abu-Ameerh; Sawsan F Mohammed; Mona T Mohammad; Osama H Ababneh; Muawyah D Al-Bdour
Journal:  Saudi J Ophthalmol       Date:  2013-07-01

6.  Cerebral venous sinus thrombosis in Behçet's disease: a retrospective case-control study.

Authors:  Jing Shi; Xinxiang Huang; Guohua Li; Li Wang; Jinjing Liu; Yan Xu; Xiaofeng Zeng; Wenjie Zheng
Journal:  Clin Rheumatol       Date:  2017-06-14       Impact factor: 2.980

7.  Assessment of genotoxicity associated with Behcet's disease using sister-chromatid exchange assay: vitamin E versus mitomycin C.

Authors:  Omar F Khabour; Khaldon Alawneh; Etizaz Al-Kofahi; Fahmee Mesmar
Journal:  Cytotechnology       Date:  2014-05-23       Impact factor: 2.058

8.  Alterations of aqueous flare and cells detected by laser flare-cell photometry in patients with Behcet's disease.

Authors:  Peizeng Yang; Wang Fang; Xiangkun Huang; Hongyan Zhou; Li Wang; Bo Jiang
Journal:  Int Ophthalmol       Date:  2008-05-15       Impact factor: 2.031

9.  Pattern of uveitis in Behçet's disease in a referral center in Tunisia, North Africa.

Authors:  Moncef Khairallah; Sonia Attia; Salim Ben Yahia; Salah Jenzeri; Rim Ghrissi; Bechir Jelliti; Sonia Zaouali; Riadh Messaoud
Journal:  Int Ophthalmol       Date:  2008-03-26       Impact factor: 2.031

10.  Hypericum perforatum modulates apoptosis and calcium mobilization through voltage-gated and TRPM2 calcium channels in neutrophil of patients with Behcet's disease.

Authors:  Mustafa Nazıroğlu; Mehmet Sahin; Bilal Ciğ; Mehmet Aykur; Ijlal Erturan; Yunus Ugan
Journal:  J Membr Biol       Date:  2014-01-23       Impact factor: 1.843

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