behaperet病神经系统受累的表现和预测因素。

IF 1.4 4区 医学 Q3 RHEUMATOLOGY
ARP Rheumatology Pub Date : 2025-04-01
Margarida Lucas Rocha, Roberto Pereira da Costa, Ana Teodósio Chícharo, Joana Martins-Martinho, Carla Macieira, Cristina Ponte, Nikita Khmelinskii
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引用次数: 0

摘要

背景:behet病(BD)是一种主要影响皮肤粘膜组织的多系统炎症性疾病。中枢神经系统(CNS)受累,神经性双相障碍(NBD),是双相障碍潜在的严重表现,患病率不同(1-59%)。目的:我们的目的是表征中枢神经系统受累的BD患者,并确定这种临床亚型的预测因素。方法:我们进行了一项单中心观察性回顾性研究,数据来自2014年10月至2023年5月在葡萄牙风湿病登记处(Reuma.pt)登记的符合2013年国际BD标准的患者。根据NBD诊断的国际共识推荐标准定义NBD。收集了人口统计学、临床和治疗数据。结果:我们纳入157例BD患者,其中116例(74%)为女性,127例(81%)为白种人,诊断时的平均±SD年龄为32.0±12.2岁,中位(IQR)随访时间为11.0(11.8)年。24例(15%)患者被诊断为NBD, 2例(1%)患者在发病时被确诊。NBD诊断的平均年龄为31.6±8.7岁,发病4.7(1.0)年。在NBD患者中,15例(63%)有实质性中枢神经系统受累,8例(33%)无实质中枢神经系统受累,1例(4%)有混合性中枢神经系统受累。与非NBD患者相比,NBD患者更有可能是非高加索人(27%对17%,p=0.026),发病时有生殖器溃疡(68%对34%,p=0.002),在病程中有眼部表现(58%对35%,p=0.028)。NBD患者更频繁地接受全身性糖皮质激素(100%对78%,p=0.008)和常规合成改善疾病的抗风湿药物(86%对62%,p=0.035),特别是环磷酰胺(48%对1%)。结论:总之,我们的队列显示CNS受累的患病率为15%,实质影响是主要形式。发病时的生殖器溃疡和眼部表现是NBD的独立预测因素,可作为识别高危患者的潜在临床标志物。在这些患者中观察到的高死亡率强调了NBD的严重性和及时识别的迫切需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Manifestations and predictors of neurologic involvement in Behçet's disease.

Background: Behçet's disease (BD) is a multisystem inflammatory disorder primarily affecting mucocutaneous tissues. Central nervous system (CNS) involvement, Neuro-BD (NBD), is a potentially severe manifestation of BD with a variable prevalence (1-59%).

Aims: We aimed to characterize BD patients with CNS involvement and to identify predictors of this clinical subtype.

Methods: We performed a single-centre observational retrospective study using data from patients fulfilling the 2013 International Criteria for BD registered at the Rheumatic Diseases Portuguese Registry (Reuma.pt) between October 2014 and May 2023. NBD was defined according to International Consensus Recommendation Criteria for NBD diagnosis. Demographic, clinical and treatment data were collected.

Results: We included 157 patients with BD, 116 (74%) of them were females and 127 (81%) Caucasian with a mean±SD age at diagnosis of 32.0±12.2 years and the median (IQR) follow-up was 11.0 (11.8) years. NBD was diagnosed in 24 (15%) patients, with two (1%) cases identified at disease onset. The mean age at NBD diagnosis was 31.6±8.7 years, occurring 4.7 (1.0) years after BD onset. Among NBD patients, 15 (63%) had parenchymal, eight (33%) non-parenchymal and one (4%) mixed CNS involvement. Compared to patients without NBD, those with NBD were more likely to be non-Caucasian (27% vs 17%, p=0.026), have genital ulcers at disease onset (68% vs 34%, p=0.002) and present with ocular manifestations during the disease course (58% vs 35%, p=0.028). NBD patients more frequently received systemic glucocorticoids (100% vs 78%, p=0.008) and conventional synthetic disease-modifying anti-rheumatic drugs (86% vs 62%, p=0.035), particularly cyclophosphamide (48% vs 1%, p<0.001). Mortality was also significantly higher among NBD (13% vs 2%, p=0.026). On multivariable analysis, genital ulcers at presentation (OR 4.50, 1.68-12.06) and ocular involvement during the disease course (OR 2.69, 1.01-6.76) were independent predictors of CNS involvement.

Conclusion: In summary, our cohort showed a 15% prevalence of CNS involvement, with parenchymal affection being the predominant form. Genital ulcers at onset and ocular manifestations emerged as independent predictors of NBD, serving as potential clinical markers for identifying high-risk patients. The high mortality rate observed among these patients underscores the severity of NBD and the critical need for prompt recognition.

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