Almansouri Abdulrahman Y, Alsindi Eman, Almani Ibraheem, Basalama Mohmed, Attar Suzan, Abdulaziz Sultana
Division of Rheumatology, Department of Medicine, King Fahad Hospital, Jeddah, Saudi Arabia.
Department of Medicine, King Faisal Specialist Hospital and Research Centre, Madinah, Saudi Arabia.
Curr Rheumatol Rev. 2024 Oct 21. doi: 10.2174/0115733971326045241016070431.
BACKGROUND/AIM: Earlier treatment in axial spondyloarthritis (axSpA) was proposed to alter disease prognosis in this often-challenging condition. We aimed to assess the proportion of patients and prognostic factors associated with axSpA remission.
The aim was to determine the number of patients with Ankylosing Spondylitis Disease Activity Score with C-reactive protein (ASDAS-CRP) of <2.1 (inactive/moderate disease activity). We also evaluated global functioning and health using the Assessment of Spondyloarthritis International Society-Health Index (ASAS-HI).
Patients with axSpA who were receiving targeted synthetic/biological disease- modifying anti-rheumatic drug (ts/bDMARDs) treatments and visited the rheumatology units at two tertiary-care centers between December 2021 and December 2022 were prospectively interviewed. Data regarding patient demographics, disease features, active and previous ts/bDMARDs treatments, and disease activity scores were obtained. Patients were assessed using the ASDAS- CRP, ASDAS-erythrocyte sedimentation rate (ASDAS-ESR), Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), and ASAS-HI.
Overall, 60 patients with axSpA were included in this study (women, n = 35); 25 (41.7%) and 36 (62.1%) achieved an ASDAS-CRP of <2.1 and an ASAS-HI of ≤5 (good health), respectively. Out of the 60 patients, 75% (n = 45) were treated with anti-tumor necrosis factor. Factors associated with achieving the target ASDAS-CRP included age (p = 0.019), sex (p = 0.015), employment status (p = 0.015), education level (p = 0.030), and the number of previous ts/bDMARDs treatments (p = 0.019). Additionally, the ASDAS-CRP strongly correlated with spinal pain and moderately correlated with the ASAS-HI, BASDAI, and the number of previous ts/bDMARDs treatments.
Remission was observed in 41.7% of patients, indicating a challenge in achieving target disease activity. However, 62.1% attained good health. Achieving remission was associated with younger age, male sex, a higher level of education, lower level of spinal pain, better global function by ASAS-HI, employment, and receiving their first ts/bDMARDs treatment. Our findings may potentially improve disease prognosis with the earlier use of ts/bDMARDs in those without favorable features by implementing an early axSpA intervention strategy.
背景/目的:对于强直性脊柱炎(axSpA)这种常具有挑战性的疾病,早期治疗被认为可改变疾病预后。我们旨在评估axSpA缓解患者的比例及相关预后因素。
确定强直性脊柱炎疾病活动度评分(采用C反应蛋白,即ASDAS-CRP)<2.1(疾病活动度为不活动/中度)的患者数量。我们还使用国际脊柱关节炎协会健康指数(ASAS-HI)评估整体功能和健康状况。
对2021年12月至2022年12月期间在两家三级医疗中心的风湿病科接受靶向合成/生物改善病情抗风湿药物(ts/bDMARDs)治疗的axSpA患者进行前瞻性访谈。获取了患者的人口统计学数据、疾病特征、正在使用及既往使用的ts/bDMARDs治疗情况以及疾病活动度评分。使用ASDAS-CRP、ASDAS-红细胞沉降率(ASDAS-ESR)、巴斯强直性脊柱炎疾病活动指数(BASDAI)和ASAS-HI对患者进行评估。
本研究共纳入60例axSpA患者(女性35例);分别有25例(41.7%)和36例(62.1%)患者的ASDAS-CRP<2.1以及ASAS-HI≤5(健康状况良好)。在这60例患者中,75%(n = 45)接受了抗肿瘤坏死因子治疗。与达到目标ASDAS-CRP相关的因素包括年龄(p = 0.019)、性别(p = 0.015)、就业状况(p = 0.015)、教育水平(p = 0.030)以及既往ts/bDMARDs治疗的次数(p = 0.019)。此外,ASDAS-CRP与脊柱疼痛强烈相关,与ASAS-HI、BASDAI以及既往ts/bDMARDs治疗的次数中度相关。
41.7%的患者实现了缓解,这表明实现疾病活动度目标具有挑战性。然而,62.1%的患者健康状况良好。实现缓解与年龄较轻、男性、教育水平较高、脊柱疼痛程度较低、ASAS-HI评估的整体功能较好、就业以及首次接受ts/bDMARDs治疗有关。我们的研究结果可能通过对那些无有利特征的患者实施早期axSpA干预策略,早期使用ts/bDMARDs来潜在地改善疾病预后。