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戈利木单抗可减少活动性强直性脊柱炎患者的睡眠障碍:一项随机、安慰剂对照试验的结果。

Golimumab reduces sleep disturbance in patients with active ankylosing spondylitis: results from a randomized, placebo-controlled trial.

机构信息

Oregon Health & Science University, Portland, OR 97239, USA.

出版信息

Arthritis Care Res (Hoboken). 2010 Sep;62(9):1266-71. doi: 10.1002/acr.20233.

Abstract

OBJECTIVE

To evaluate the effect of golimumab on sleep disturbance in patients with active ankylosing spondylitis (AS).

METHODS

Golimumab was studied in a multicenter, randomized, placebo-controlled study (GO-RAISE). At baseline, 356 patients were randomly assigned in a 1.8:1.8:1 ratio to subcutaneous golimumab 50 mg, 100 mg, or placebo every 4 weeks. Sleep disturbance was assessed using the Jenkins Sleep Evaluation Questionnaire (JSEQ), which was administered at baseline, week 14, and week 24. Treatment effect was evaluated using analysis of variance on the van der Waerden normal scores.

RESULTS

Median JSEQ scores at baseline were 9.0 in the placebo group, 10.0 in the 50-mg group, and 11.0 in the 100-mg group, indicating moderate to severe sleep disturbance. Patients who received golimumab showed significantly greater median improvement from baseline in JSEQ scores compared with placebo at week 14 (-3.0 versus 0.0; P < 0.001) and week 24 (-3.0 versus -1.0; P < 0.001). Changes from baseline in JSEQ scores significantly correlated with changes from baseline in Short Form 36 summary scores, Bath AS Functional Index scores, total back pain, night back pain, and Bath AS Disease Activity Index scores. Multiple regression analyses indicated that improvement in the night back pain score was the most consistent predictor of change in JSEQ score or reduction in sleep disturbance.

CONCLUSION

Patients with active AS showed significant sleep disturbance at baseline due to underlying pain associated with AS. Treatment with subcutaneous golimumab every 4 weeks significantly reduced sleep disturbance and improved health-related quality of life.

摘要

目的

评估戈利木单抗治疗活动期强直性脊柱炎(AS)患者睡眠障碍的效果。

方法

戈利木单抗的研究采用多中心、随机、安慰剂对照试验(GO-RAISE)。在基线时,356 例患者按 1.8:1.8:1 的比例随机分配接受皮下注射戈利木单抗 50mg、100mg 或安慰剂,每 4 周 1 次。睡眠障碍采用詹金斯睡眠评估问卷(JSEQ)进行评估,在基线、第 14 周和第 24 周进行评估。采用范德瓦尔登正态评分的方差分析评估治疗效果。

结果

安慰剂组基线时 JSEQ 评分中位数为 9.0,50mg 组为 10.0,100mg 组为 11.0,表明存在中重度睡眠障碍。与安慰剂组相比,接受戈利木单抗治疗的患者在第 14 周(-3.0 分比 0.0 分;P<0.001)和第 24 周(-3.0 分比-1.0 分;P<0.001)JSEQ 评分的中位数改善更显著。JSEQ 评分从基线的变化与简明健康状况调查问卷 36 项简表评分、巴斯强直性脊柱炎功能指数评分、总背痛、夜间背痛和巴斯强直性脊柱炎疾病活动指数评分从基线的变化显著相关。多元回归分析表明,夜间背痛评分的改善是 JSEQ 评分变化或睡眠障碍减轻的最一致预测因素。

结论

活动期 AS 患者由于与 AS 相关的基础疼痛而在基线时出现明显的睡眠障碍。每 4 周皮下注射戈利木单抗治疗可显著减轻睡眠障碍并改善健康相关生活质量。

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