Department of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Arthritis Research UK Centre for Epidemiology, Centre for Musculoskeletal Research, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Rheumatology (Oxford). 2018 May 1;57(5):835-843. doi: 10.1093/rheumatology/kex528.
To investigate the relationship between depressive symptoms and treatment response and disease activity in RA over a 1-year follow-up.
Data from the British Society for Rheumatology Biologics Register were used, representing 18 421 RA patients receiving biologic treatment. Depressive symptoms were identified through one of three assessments: reporting a history of depression, the Medical Outcomes Survey 36-item Short Form or the EuroQol five-dimension scale. Logistic regression analyses examined the relationship between baseline depressive symptoms and odds of good treatment response by 1 year. Multilevel models addressed the association between baseline depressive symptoms and disease activity outcomes over 1-year follow-up, adjusting for age, gender, disease duration, comorbidities and baseline disease activity and physical disability.
Depression symptoms at biologic treatment initiation were associated with 20-40% reduced odds of achieving a good treatment response at 1 year. Depressive symptoms at baseline also associated with reduced improvement in disease activity over the course of follow-up. Patients with a history of depression or reporting symptoms of depression according to the EuroQol five-dimension scale showed reduced improvement in tender and swollen joints, patient global assessment and ESR over 1-year follow-up. Patients with depression symptoms according to the 36-item Short Form showed reduced improvement in tender and swollen joints, but not ESR or patient global assessment.
Experiencing symptoms of depression at the start of biologics treatment may reduce the odds of achieving a good treatment response, and reduce improvement in disease activity over time. Depression should be managed as part of routine clinical care to optimize treatment outcomes.
在为期 1 年的随访中,调查 RA 患者抑郁症状与治疗反应和疾病活动之间的关系。
使用英国风湿病学会生物制剂登记处的数据,代表 18421 名接受生物制剂治疗的 RA 患者。抑郁症状通过以下三种评估之一确定:报告有抑郁病史、医疗结果调查 36 项简明健康调查问卷或欧洲五维健康量表。逻辑回归分析检查了基线抑郁症状与 1 年内良好治疗反应的可能性之间的关系。多层次模型解决了基线抑郁症状与 1 年随访期间疾病活动结果之间的关联,调整了年龄、性别、疾病持续时间、合并症以及基线疾病活动和身体残疾。
生物治疗开始时出现抑郁症状与 1 年内达到良好治疗反应的可能性降低 20%-40%有关。基线时的抑郁症状也与疾病活动随时间的改善减少有关。有抑郁病史或根据欧洲五维健康量表报告抑郁症状的患者在 1 年随访期间,其压痛关节和肿胀关节、患者整体评估和 ESR 的改善减少。根据 36 项短表报告有抑郁症状的患者压痛关节和肿胀关节的改善减少,但 ESR 或患者整体评估没有减少。
在生物制剂治疗开始时出现抑郁症状可能会降低达到良好治疗反应的可能性,并随时间减少疾病活动的改善。应将抑郁作为常规临床护理的一部分进行管理,以优化治疗结果。