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Beh?et's disease and familial Mediterranean fever: Two sides of the same coin or just an association? A cross-sectional study

机译:ET的疾病和家族地中海发热:同一硬币的两侧或只是一个协会? 横断面研究

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ABSTRACTBackground: Familial Mediterranean fever (FMF) is a genetic disease, characterized by attacks of fever, arthritis, serositis and pain. Beh?et's disease (BD) is an inflammatory disorder with a genetic basis, characterized by oral and genital ulcers, uveitis, pustular erythematous cutaneous lesions, arthritis, central nervous system involvement and possible vascular manifestations such as venous thrombosis, arteritis and aneurysms. Objectives: To investigate the association and actual differentiation between these two entities in a large-scale population-based study.Methods: Data for this study was collected from the databases of "Clalit Health Services", the largest state-mandated health service organization in Israel. All adult members diagnosed with BD were included (n = 892) and as well as their age- and sex-matched controls (n = 4444), creating a cross-sectional population-based study. Medical records of all subjects were analyzed for documented FMF. A logistic regression model was done to estimate how BD, age, gender, BMI, ethnicity and socioeconomic status contributed as risk factors for FMF. Results: The proportion of FMF in patients with BD increased compared with those reported in controls (5.83% and 0.23%, respectively, P b 0.001). This coexistence was prominent among both sex groups but was much stronger among female BD patients (females with OR of 177 and of 8.4 in males, P b 0.001). In a multivariate analysis, BD was identified as an independent risk factor for FMF (OR 25.16,95% CI 13-53.3).Conclusion: BD diagnosis was found to be independently associated with higher incidence of FMF, especially in females, people of Arab descent and BMI N 30. Our data imply that understating the differentiation between FMF and BD is not evident and clear in a real-life population of patients with BD.? 2016 European Federation of Internal Medicine. Published by Elsevier B.V. All rights reserved.
机译:AbstractBackground:家族地中海热(FMF)是一种遗传疾病,其特征是发烧,关节炎,浆膜和疼痛的攻击。 ET的疾病(BD)是一种遗传障碍的炎症性疾病,其特征在于口服和生殖器溃疡,葡萄炎,脓肿性红斑皮肤病变,关节炎,中枢神经系统受累和可能的血管表现,如静脉血栓形成,动脉瘤和动脉瘤等可能的血管表现。目标:调查这两个实体在基于大规模的学习中的关联和实际差异。方法:本研究的数据是从“Clalit卫生服务”的数据库中,是最大的国家任务卫生服务组织以色列。包括诊断出BD的所有成员(n = 892),以及其年龄和性别匹配的对照(n = 4444),产生基于横截面的人群的研究。分析了所有受试者的病历,以记录的FMF。逻辑回归模型是为了估计BD,年龄,性别,BMI,种族和社会经济地位如何为FMF的危险因素贡献。结果:与对照中报道的人相比,BD患者FMF的比例增加(分别为5.83%和0.23%,p b 0.001)。这种共存在两个性别群体中都很突出,但在女性BD患者中更强大(男性为177例,男性177人,P <0.001)。在多变量分析中,BD被鉴定为FMF的独立危险因素(或25.16,95%CI 13-53.3)。结论:发现BD诊断与FMF的发病率较高,特别是在女性中,阿拉伯人下降和BMI N 30.我们的数据意味着低估FMF和BD之间的差异并不明显,并且在BD患者的现实寿命中清楚地清楚。 2016年欧洲内科联合会。 elsevier b.v出版。保留所有权利。

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