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乳铁蛋白治疗对新冠后综合征患者症状及身体机能的影响:一项随机、双盲、安慰剂对照试验

Effect of lactoferrin treatment on symptoms and physical performance in long COVID patients: a randomised, double-blind, placebo-controlled trial.

作者信息

Redel Anne-Lotte, Miry Fatana, Hellemons Merel Elise, Oswald Laurien Maria Amarentia, Braunstahl Gerrit Johannes

机构信息

Department of Pulmonology, Franciscus Gasthuis & Vlietland, Rotterdam, the Netherlands.

Department of Pulmonology, Erasmus University Medical Center, Rotterdam, the Netherlands.

出版信息

ERJ Open Res. 2024 Jul 29;10(4). doi: 10.1183/23120541.00031-2024. eCollection 2024 Jul.

Abstract

BACKGROUND

Long COVID is a heterogeneous condition with a variety of symptoms that persist at least 3 months after SARS-CoV-2 infection, often with a profound impact on quality of life. Lactoferrin is an iron-binding glycoprotein with anti-inflammatory and antiviral properties. Current hypotheses regarding long COVID aetiology include ongoing immune activation, viral persistence and auto-immune dysregulation. Therefore, we hypothesised that long COVID patients may potentially benefit from lactoferrin treatment. The aims of the present study were to investigate the effect of lactoferrin on various long COVID domains: fatigue, anxiety, depression, cognitive failure and muscle strength.

METHODS

We performed a randomised, double-blind, placebo-controlled trial in long COVID patients aged 18-70 years within 12 months after proven SARS-CoV-2 infection. Patients were randomised (1:1) to 6 weeks of lactoferrin (1200 mg daily) or placebo. At three hospital visits (T0, T6 and T12 weeks), patient-reported outcome measures were collected, physical performance tests were performed and blood was drawn. The difference in fatigue at T6 was the primary outcome.

RESULTS

72 participants were randomised to lactoferrin (n=36) or placebo (n=36). We found a significant decrease in fatigue, as measured with the Fatigue Assessment Scale, between T0 and T6 in both study arms, but without significant difference between the study arms (lactoferrin: 3.9, 95% CI 2.3-5.5, p=0.007; placebo: 4.1, 95% CI 2.3-5.9, p=0.013). No significant differences were found in any of the other outcomes in favour of the lactoferrin arm at T6 or T12.

CONCLUSION

Although both long COVID arms showed improved clinical outcomes at T6, the improvement did not continue until T12. Lactoferrin provided no benefit in terms of fatigue, other patient-reported outcome measures or physical functioning.

摘要

背景

新冠后遗症是一种异质性疾病,具有多种症状,在严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染后至少持续3个月,常对生活质量产生深远影响。乳铁蛋白是一种具有抗炎和抗病毒特性的铁结合糖蛋白。目前关于新冠后遗症病因的假说包括持续的免疫激活、病毒持续存在和自身免疫失调。因此,我们推测新冠后遗症患者可能会从乳铁蛋白治疗中获益。本研究的目的是调查乳铁蛋白对新冠后遗症各个方面的影响:疲劳、焦虑、抑郁、认知功能障碍和肌肉力量。

方法

我们对确诊感染SARS-CoV-2后12个月内年龄在18至70岁的新冠后遗症患者进行了一项随机、双盲、安慰剂对照试验。患者被随机(1:1)分为两组,分别接受为期6周的乳铁蛋白治疗(每日1200毫克)或安慰剂治疗。在三次医院就诊时(第0、6和12周),收集患者报告的结局指标,进行身体机能测试并采集血液样本。第6周时疲劳程度的差异是主要结局指标。

结果

72名参与者被随机分为乳铁蛋白组(n = 36)或安慰剂组(n = 36)。我们发现,在两个研究组中,用疲劳评估量表测量的疲劳程度在第0周和第6周之间均有显著下降,但两组之间无显著差异(乳铁蛋白组:3.9,95%置信区间2.3 - 5.5,p = 0.007;安慰剂组:4.1,95%置信区间2.3 - 5.9,p = 0.013)。在第6周或第12周时,在任何其他结局指标方面,均未发现有利于乳铁蛋白组的显著差异。

结论

尽管两个新冠后遗症组在第6周时临床结局均有所改善,但这种改善在第12周时并未持续。乳铁蛋白在疲劳、其他患者报告的结局指标或身体机能方面未显示出益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3327/11284587/29c66520a0f7/00031-2024.01.jpg

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