Department of Internal Medicine, Division of Rheumatology, Maastricht University Medical Centre, PO Box 5800, Maastricht, 6202 AZ, The Netherlands.
Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, the Netherlands.
Arthritis Res Ther. 2020 Sep 29;22(1):225. doi: 10.1186/s13075-020-02305-w.
Patients with ankylosing spondylitis (AS) are at increased risk of depression. This increased risk has been hypothesized to be solely secondary due to AS-related symptoms, or additionally due to a common inflammatory pathway. From a clinical perspective, it is important to know whether treatment with tumor necrosis factor alpha inhibitors reduces depressive symptoms, while from a pathophysiological point of view, it would be insightful to understand whether such an effect would be a direct result of reduced inflammation, the result of reduced AS-related symptoms, or both. The objective of this study was to evaluate the effect of infliximab on depressive symptoms in patients with AS in a randomized-controlled trial setting.
Data were retrieved from a subgroup of patients from the AS Study for the Evaluation of Recombinant Infliximab Therapy (ASSERT). Patients were randomly allocated to infliximab (n = 16) or placebo (n = 7) until week 24, after which all received infliximab until week 54. Associations between treatment group and depressive symptoms, measured with the Center for Epidemiological Studies Depression scale (CES-D, range 0-60 (best-worst)) at baseline and over time, were explored with generalized estimating equations (GEE).
Mean CES-D score at baseline was 15.5 (SD 9.3) in the infliximab group and 17.3 (SD 5.7) in the placebo group. Twelve patients (52%) had a CES-D score > 16, suggestive for clinical depression. After 24 weeks, mean CES-D had decreased to 9.5 (SD 11.4) in the infliximab group, but was 18.0 (SD 6.9) in the placebo group. GEE revealed larger improvements in depressive symptoms (B = - 6.63, 95%CI - 13.35 to 0.09) and odds of possible depression (OR = 0.02, 95%CI 0.00 to 0.72) in the infliximab group, compared to the placebo group. Both associations largely disappeared when adjusted for self-reported disease activity and/or physical function. Additional adjustment for C-reactive protein (CRP) did not change results.
Depressive symptoms are common in patients with AS and active disease. Infliximab improves these depressive symptoms in AS when compared to placebo by improving disease symptoms. We did not find an indication for a direct link between CRP-mediated inflammation and depressive symptoms.
Trial registration (ASSERT): NCT00207701 . Registered on September 21, 2005 (retrospectively registered).
强直性脊柱炎(AS)患者患抑郁症的风险增加。这种风险增加的假设仅归因于与 AS 相关的症状,或者还归因于共同的炎症途径。从临床角度来看,了解肿瘤坏死因子 α 抑制剂的治疗是否可以减轻抑郁症状非常重要,而从病理生理学角度来看,了解这种影响是否是炎症减轻的直接结果、与 AS 相关症状减轻的结果或两者兼而有之,将具有洞察力。本研究的目的是在随机对照试验环境中评估英夫利昔单抗对 AS 患者抑郁症状的影响。
数据来自 AS 研究评估重组英夫利昔单抗治疗(ASSERT)的亚组患者。患者被随机分配至英夫利昔单抗(n=16)或安慰剂(n=7)组,直至第 24 周,此后所有患者均接受英夫利昔单抗治疗至第 54 周。使用广义估计方程(GEE)探索基线和随时间变化时治疗组与抑郁症状(用流行病学研究中心抑郁量表(CES-D,范围 0-60(最差-最好))测量)之间的关联。
英夫利昔单抗组基线时 CES-D 平均得分为 15.5(SD 9.3),安慰剂组为 17.3(SD 5.7)。12 名患者(52%)的 CES-D 评分>16,提示存在临床抑郁。24 周后,英夫利昔单抗组 CES-D 平均得分降至 9.5(SD 11.4),而安慰剂组为 18.0(SD 6.9)。GEE 显示,与安慰剂组相比,英夫利昔单抗组抑郁症状(B=−6.63,95%CI−13.35 至 0.09)和可能出现抑郁的几率(OR=0.02,95%CI 0.00 至 0.72)均有较大改善。当调整自我报告的疾病活动度和/或身体功能时,这两种关联均基本消失。进一步调整 C 反应蛋白(CRP)并不能改变结果。
抑郁症状在 AS 患者中很常见,且与疾病活动有关。与安慰剂相比,英夫利昔单抗通过改善疾病症状来改善 AS 患者的这些抑郁症状。我们没有发现 CRP 介导的炎症与抑郁症状之间存在直接联系的迹象。
ASSERT 试验注册:NCT00207701。于 2005 年 9 月 21 日注册(追溯性注册)。