伴有活动性疾病的轴性脊柱炎患者是否有更大的疾病负担和工作障碍?轴性脊柱炎国际地图(IMAS)结果

Marco Garrido-Cumbrera , Denis Poddubnyy , Fernando Sommerfleck , Christine Bundy , Souzi Makri , José Correa-Fernández , Shashank Akerkar , Jo Lowe , Elie Karam , Victoria Navarro-Compán
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引用次数: 0

摘要

背景:在国际轴性脊柱炎地图(IMAS)研究的全球大量患者样本中,评估轴性脊柱炎(axSpA)临床活动性疾病的患病率及其相关因素。方法simas是一项针对5557例axSpA患者的横断面在线调查(2017-2022)。患者分为活动性疾病组(BASDAI≥4)和非活动性疾病组(BASDAI <4)。评估的因素包括社会人口统计学、生活方式、患者报告的结果、就业、疾病特征、肌肉骨骼外表现和治疗。采用按性别分层的Logistic回归分析评价调查因素与活动性疾病的关系。结果本研究共纳入5295例对BASDAI量表有反应的患者,其中欧洲3231例,北美770例,亚洲600例,拉丁美洲548例,非洲146例。平均年龄43.8±12.9岁,女性占55.4%。患者报告BASDAI平均为5.4(±2.1),其中75%为活动性疾病(BASDAI≥4)。在南非,87.0%的患者报告患有活动性疾病,而亚洲为68.5%。多变量logistic回归显示,活动性疾病与较高的功能限制、较高的脊柱僵硬、由于axSpA导致的找工作困难以及较差的心理健康状况在两性中均存在关联。对于男性,较年轻和较短的诊断延迟,以及对于女性,没有身体活动和存在炎症性肠病与活动性疾病相关。结论3 / 4的axSpA患者报告临床活动性疾病,其中南非的活动性疾病比例较高,亚洲的比例较低。我们的研究结果强调了axSpA临床疾病活动概念的复杂性,以及在患者管理、护理和治疗中采用整体方法的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Do patients with axial spondyloarthritis with active disease suffer from greater disease burden and work impairment? Results from the International Map of Axial Spondyloarthritis (IMAS)

Background

To assess the prevalence of clinically active disease in axial spondyloarthritis (axSpA) and its associated factors in a large global sample of patients from the International Map of Axial Spondyloarthritis (IMAS) study.

Methods

IMAS is a cross-sectional online survey (2017–2022) of 5557 axSpA patients. Patients were divided between those with active disease (BASDAI ≥4) and without active disease (BASDAI <4). The factors evaluated were sociodemographic, lifestyle, patient-reported outcomes, employment, disease characteristics, extra-musculoskeletal manifestations, and treatment. Logistic regression analysis stratified by gender were used to evaluate the relationship between investigated factors and active disease.

Results

In the present study, 5295 patients who had responded to the BASDAI scale were included in the present study: 3231 were from Europe, 770 from North America, 600 from Asia, 548 from Latin America, and 146 from Africa. The mean age was 43.8 ± 12.9 years and 55.4% were females. Patients reported a mean BASDAI of 5.4 (±2.1) with 75% having active disease (BASDAI ≥4). In South Africa, 87.0% of patients reported having active disease, compared to 68.5% in Asia. Multivariable logistic regression showed an association of active disease with higher functional limitation, greater spinal stiffness, difficulty finding a job due to axSpA and worse mental health in both genders. For males, younger age and shorter diagnostic delay, and for females, no physical activity and presence of inflammatory bowel disease were associated with active disease.

Conclusions

Three quarters of patients with axSpA reported clinically active disease, with higher proportion of patients with active disease in South Africa and lower proportion in Asia. Our results underline the complexity of the clinical disease activity concept in axSpA and the need for a holistic approach in the patient management, care and treatment.
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