Literature DB >> 23881265

Systemic involvements and preferred treatments in a large cohort of Behçet's disease.

Sedat Yilmaz1, Omer Karadag, Veli Yazisiz, Battal Altun, Mustafa Gezer, Murat Karaman, Muhammet Cinar, Hakan Erdem, Salih Pay, Ayhan Dinc.   

Abstract

The immunosuppressive drugs are widely used in systemic involvements of Behçet's disease. This study is aimed to investigate the extent of clinical involvement and preferred treatment approaches for type of involvements in Behçet's patients from the whole country. All patients with the diagnosis of Behçet's disease were enrolled to the study. These patients analyzed whether they fulfill the International Study Group Criteria, and only those were further evaluated. Demographic and clinical characteristics, laboratory results and treatments ever used were recorded. Further analysis is done regarding clinical manifestations and preferred therapeutic approaches. A total of 863 patients with the diagnosis of Behçet's disease were detected, but 682 of them (female/male: 113/569) found to be appropriate for analysis. The remaining patients were included to the analysis. The frequencies of articular, ophthalmic and vascular involvement were 49, 43 and 21 %, respectively. Colchicine and corticosteroids were the most preferred agents. The immunosuppressive agents frequently used for organ involvements were azathioprine, cyclosporine A, interferon-α, sulphasalazine and cyclophosphamide with decreasing order of frequency. In this relatively young population composed from all over the country, the frequency of ophthalmologic, venous and neurological involvement is less frequent than previous reported cohorts. Azathioprine and cyclosporine were the drugs of choice as a chronic immunosuppressive agent in patients with organ involvement. The previously reported increased frequencies in other cohorts could be a result of the reference of severe patients to dedicated centers.

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Year:  2013        PMID: 23881265     DOI: 10.1007/s00296-013-2830-0

Source DB:  PubMed          Journal:  Rheumatol Int        ISSN: 0172-8172            Impact factor:   2.631


  13 in total

1.  Clinical manifestations of Behçet's disease in 137 Italian patients: results of a multicenter study.

Authors:  N Pipitone; L Boiardi; I Olivieri; F Cantini; F Salvi; R Malatesta; R La Corte; G Triolo; A Ferrante; D Filippini; G Paolazzi; P Sarzi-Puttini; G Restuccia; C Salvarani
Journal:  Clin Exp Rheumatol       Date:  2004       Impact factor: 4.473

Review 2.  Standard and novel therapeutic approaches to Behçet's disease.

Authors:  Ahmet Gul
Journal:  Drugs       Date:  2007       Impact factor: 9.546

3.  EULAR recommendations for the management of Behçet disease.

Authors:  G Hatemi; A Silman; D Bang; B Bodaghi; A M Chamberlain; A Gul; M H Houman; I Kötter; I Olivieri; C Salvarani; P P Sfikakis; A Siva; M R Stanford; N Stübiger; S Yurdakul; H Yazici
Journal:  Ann Rheum Dis       Date:  2008-01-31       Impact factor: 19.103

Review 4.  Criteria for diagnosis of Behçet's disease. International Study Group for Behçet's Disease.

Authors: 
Journal:  Lancet       Date:  1990-05-05       Impact factor: 79.321

5.  Major vessel thrombosis in Behçet's disease: the dilemma of anticoagulant therapy - the approach of rheumatologists from different countries.

Authors:  Oshrat E Tayer-Shifman; Emire Seyahi; Johannes Nowatzky; Eldad Ben-Chetrit
Journal:  Clin Exp Rheumatol       Date:  2012-10-17       Impact factor: 4.473

6.  Behçet disease: clinical features and management in a Brazilian tertiary hospital.

Authors:  Ana Cecília Diniz Oliveira; Ana Letícia Pirozzi Buosi; Lívia Almeida Dutra; Alexandre Wagner Silva de Souza
Journal:  J Clin Rheumatol       Date:  2011-12       Impact factor: 3.517

7.  Behçet's disease in Saudi Arabia.

Authors:  A N al-Dalaan; S R al Balaa; K el Ramahi; Z al-Kawi; S Bohlega; S Bahabri; M A al Janadi
Journal:  J Rheumatol       Date:  1994-04       Impact factor: 4.666

8.  Behçet's disease in Tunisia. Demographic, clinical and genetic aspects in 260 patients.

Authors:  M H Houman; H Neffati; A Braham; O Harzallah; M Khanfir; M Miled; K Hamzaoui
Journal:  Clin Exp Rheumatol       Date:  2007 Jul-Aug       Impact factor: 4.473

Review 9.  Behçet's syndrome.

Authors:  Sebahattin Yurdakul; Hasan Yazici
Journal:  Best Pract Res Clin Rheumatol       Date:  2008-10       Impact factor: 4.098

10.  Epidemiologic and clinical survey of Behcet's disease in Korea: the first multicenter study.

Authors:  D Bang; J H Lee; E S Lee; S Lee; J S Choi; Y K Kim; B K Cho; J K Koh; Y H Won; N I Kim; S D Park; H J Ahn; Y W Lee; H Y Wang; W W Lee; H C Eun; E S Song; S W Lee; C W Lee; C J Lee; J H Park; Y W Song; S T Kim; C Y Kim; J K Park; K S Kwon
Journal:  J Korean Med Sci       Date:  2001-10       Impact factor: 2.153

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  4 in total

Review 1.  Similarities and differences between Behçet's disease and Crohn's disease.

Authors:  Veli Yazısız
Journal:  World J Gastrointest Pathophysiol       Date:  2014-08-15

Review 2.  Left ventricular intracardiac thrombus in a patient with Behçet disease successfully treated with immunosuppressive agents without anticoagulation: a case report and review of the literature.

Authors:  Tatiana Lisitsyna; Zemfira Alekberova; Pavel Ovcharov; Alexander Volkov; Julia Korsakova; Evgeni Nasonov
Journal:  Rheumatol Int       Date:  2015-06-09       Impact factor: 2.631

3.  Epidemiology and treatment of Behçet's disease in the USA: insights from the Rheumatology Informatics System for Effectiveness (RISE) Registry with a comparison with other published cohorts from endemic regions.

Authors:  Nevin Hammam; Jing Li; Michael Evans; Julia L Kay; Zara Izadi; Christine Anastasiou; Milena A Gianfrancesco; Jinoos Yazdany; Gabriela Schmajuk
Journal:  Arthritis Res Ther       Date:  2021-08-30       Impact factor: 5.606

4.  Behçet's disease in the United States: A single center descriptive and comparative study.

Authors:  Nathan C Kilian; Amr H Sawalha
Journal:  Eur J Rheumatol       Date:  2017-11-03
  4 in total

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