The effects of 3-month supplementation with synbiotic on patient-reported outcomes, exercise tolerance, and brain and muscle metabolism in adult patients with post-COVID-19 chronic fatigue syndrome (STOP-FATIGUE): a randomized Placebo-controlled clinical trial.

IF 4.1 2区 医学 Q2 NUTRITION & DIETETICS European Journal of Nutrition Pub Date : 2024-11-26 DOI:10.1007/s00394-024-03546-0
Marijana Ranisavljev, Valdemar Stajer, Nikola Todorovic, Jelena Ostojic, Jelena Helena Cvejic, Robert E Steinert, Sergej M Ostojic
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Abstract

Purpose: Considering the observed gastrointestinal issues linked to post-COVID-19 myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), beneficially modulating the gut microbiota could offer a safe, cost-effective nutritional strategy. This trial aimed to evaluate the effects of medium-term synbiotic supplementation on patient-reported outcomes, exercise tolerance, and tissue metabolism in patients with post-COVID-19 ME/CFS.

Methods: Between September 2022 and December 2023, we investigated the impact of 3-month supplementation with a synbiotic mixture including L. rhamnosus DSM 32550, Humiome® L. plantarum DSM 34532, B. lactis DSM 32269, B. longum DSM 32946, fructooligosaccharides and zinc, on predetermined primary and secondary outcome measures in twenty six post-COVID-19 ME/CFS patients utilizing a parallel-group, randomized, placebo-controlled, double-blind design.

Results: Both the synbiotic and placebo intake resulted in a significant reduction in general fatigue after 3 months compared to the baseline values (P ≤ 0.05). This was accompanied by a significant interaction effect (time vs. treatment) for post-exercise malaise (P = 0.02), with synbiotic superior to placebo to attenuate post-exercise malaise. The synbiotic also demonstrated a significant advantage over placebo in increasing choline levels at the thalamus (P = 0.02), and creatine levels at left frontal white matter (P = 0.05) and left frontal grey matter (P = 0.04).

Conclusion: Taking the synbiotic mixture for three months improves tissue metabolism and mitigates clinical features of post-COVID-19 fatigue syndrome. The presented data show promise in addressing the widespread issue of ME/CFS following the COVID-19 pandemic; however, further validation is needed before endorsing the synbiotics within this clinical context. The study is registered at ClinicalTrials.gov (NCT06013072).

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为期 3 个月的合生元补充剂对 COVID-19 后慢性疲劳综合征(STOP-FATIGUE)成年患者的患者报告结果、运动耐受性以及大脑和肌肉代谢的影响:随机安慰剂对照临床试验。
目的:考虑到观察到的与COVID-19后肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)相关的胃肠道问题,有益地调节肠道微生物群可提供一种安全、经济有效的营养策略。本试验旨在评估中期补充合生元对COVID-19后ME/CFS患者的患者报告结果、运动耐受性和组织代谢的影响:方法:在2022年9月至2023年12月期间,我们采用平行组、随机、安慰剂对照、双盲设计,对26名COVID-19后ME/CFS患者进行了为期3个月的益生菌混合物补充,包括鼠李糖DSM 32550、Humiome®植物乳杆菌DSM 34532、乳酸杆菌DSM 32269、长芽孢杆菌DSM 32946、果寡糖和锌,以研究其对预定的主要和次要结果指标的影响:结果:与基线值相比,服用合生元和安慰剂都能在三个月后显著减轻全身疲劳(P ≤ 0.05)。与此同时,运动后乏力的交互效应(时间与治疗)也很明显(P = 0.02),益生菌在减轻运动后乏力方面优于安慰剂。在提高丘脑胆碱水平(P = 0.02)、左额叶白质肌酸水平(P = 0.05)和左额叶灰质肌酸水平(P = 0.04)方面,益生菌也比安慰剂有明显优势:结论:连续三个月服用益生菌混合物可改善组织代谢,缓解 COVID-19 后疲劳综合征的临床特征。所提供的数据表明,COVID-19 大流行后,ME/CFS 这一普遍问题有望得到解决;然而,在临床上认可益生菌之前,还需要进一步的验证。该研究已在 ClinicalTrials.gov 上注册(NCT06013072)。
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来源期刊
CiteScore
10.20
自引率
2.00%
发文量
295
审稿时长
6 months
期刊介绍: The European Journal of Nutrition publishes original papers, reviews, and short communications in the nutritional sciences. The manuscripts submitted to the European Journal of Nutrition should have their major focus on the impact of nutrients and non-nutrients on immunology and inflammation, gene expression, metabolism, chronic diseases, or carcinogenesis, or a major focus on epidemiology, including intervention studies with healthy subjects and with patients, biofunctionality of food and food components, or the impact of diet on the environment.
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