Department of Internal Medicine, Stavanger University Hospital, Stavanger, Norway.
Department of Dermatology, Stavanger University Hospital, Stavanger, Norway.
Drugs. 2023 Jul;83(10):909-921. doi: 10.1007/s40265-023-01888-3. Epub 2023 May 23.
Fatigue is a frequent complaint in patients with inflammatory bowel disease. Biological drugs have demonstrated beneficial effects on some extraintestinal manifestations, but the effect on fatigue is not clear.
This study investigated the effects of biological and small molecule drugs approved for inflammatory bowel disease on fatigue.
We performed a systematic review and meta-analysis of randomized, placebo-controlled trials reporting Federal Drug Agency (FDA)-approved biological and small molecule drugs for use in ulcerative colitis and Crohn's disease in which measures of fatigue were recorded before and after treatment. Only induction studies were included. Maintenance studies were excluded. We searched Embase (Ovid), Medline (Ovid), PsycINFO (Ovid), Cinahl (EBSCOhost), Web of Science Core Collection, Cochrane Central Register of Controlled Trials, and ClinicalTrials.gov in May 2022. Risk of bias was analyzed using the Cochrane risk-of-bias tool. Standardized mean difference was used to measure the treatment effect.
A total of seven randomized controlled trials composed of 3835 patients were included in the meta-analysis. All of the studies included patients with moderately to severely active ulcerative colitis or Crohn's disease. The studies used three different generic fatigue instruments: the Functional Assessment of Chronic Illness Therapy-Fatigue and the Short Form 36 Health Survey Vitality Subscale versions 1 and 2. Overall treatment with biological or small molecule agents showed a beneficial effect compared with placebo, with a standardized mean difference of 0.25 (95% confidence interval 0.15-0.34, p < 0.001). The effect was independent of type of drug or subtype of inflammatory bowel disease.
The risk of bias was considered to be low for all domains except for missing outcome data. Even though the included studies were of high methodological quality, the review is limited by the small number of studies included and that the available studies were not designed to evaluate fatigue specifically.
Biological and small molecule drugs used in inflammatory bowel disease have a consistent, though small, beneficial effect on fatigue.
疲劳是炎症性肠病患者常见的主诉。生物制剂已被证明对一些肠外表现有效,但对疲劳的影响尚不清楚。
本研究旨在调查已批准用于炎症性肠病的生物制剂和小分子药物对疲劳的影响。
我们对报告了在接受治疗前后记录疲劳测量结果的、已批准用于溃疡性结肠炎和克罗恩病的生物制剂和小分子药物的随机、安慰剂对照试验进行了系统评价和荟萃分析。仅纳入诱导治疗研究,排除维持治疗研究。我们于 2022 年 5 月在 Embase(Ovid)、Medline(Ovid)、PsycINFO(Ovid)、Cinahl(EBSCOhost)、Web of Science 核心合集、Cochrane 对照试验中心注册库和 ClinicalTrials.gov 进行了检索。使用 Cochrane 偏倚风险工具分析偏倚风险。使用标准化均数差来衡量治疗效果。
共有 7 项随机对照试验(纳入 3835 例患者)纳入荟萃分析。所有研究均纳入中重度活动期溃疡性结肠炎或克罗恩病患者。这些研究使用了三种不同的通用疲劳量表:慢性疾病治疗功能评估-疲劳量表和健康调查简表 36 生命质量量表版本 1 和版本 2。与安慰剂相比,生物制剂或小分子药物的总体治疗效果较好,标准化均数差为 0.25(95%置信区间 0.15-0.34,p<0.001)。这种效果与药物类型或炎症性肠病亚型无关。
除结局数据缺失外,所有领域的偏倚风险均被认为较低。尽管纳入的研究方法学质量较高,但由于纳入的研究数量较少,以及现有研究并非专门设计用于评估疲劳,因此该综述存在一定的局限性。
用于炎症性肠病的生物制剂和小分子药物对疲劳有一致的、虽小但有临床意义的改善作用。