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新冠后综合征患者高剂量辅酶Q10治疗与安慰剂对照:一项随机、2期、交叉试验

High-dose coenzyme Q10 therapy versus placebo in patients with post COVID-19 condition: a randomized, phase 2, crossover trial.

作者信息

Hansen Kristoffer S, Mogensen Trine H, Agergaard Jane, Schiøttz-Christensen Berit, Østergaard Lars, Vibholm Line K, Leth Steffen

机构信息

Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.

Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

出版信息

Lancet Reg Health Eur. 2023 Jan;24:100539. doi: 10.1016/j.lanepe.2022.100539. Epub 2022 Nov 2.

Abstract

BACKGROUND

Post COVID-19 condition (PCC) is defined as symptoms lasting more than 12 weeks after developing COVID-19. Evidence of mitochondrial dysfunction has been reported in peripheral blood mononuclear cells obtained from patients with COVID-19. We hypothesized that PCC is caused by prolonged mitochondrial dysfunction. Given that coenzyme Q10 (CoQ10) can improve mitochondrial function, we examined whether high-dose CoQ10 can reduce the number and/or severity of PCC-related symptoms.

METHODS

In this placebo-controlled, double-blind, 2 × 2 crossover interventional trial, participants were recruited from two centres at Aarhus University Hospital and Gødstrup Hospital, Denmark. They were randomly assigned to receive either oral capsules of CoQ10 in a dose of 500 mg/day or placebo for 6 weeks, with crossover treatment after a 4-week washout period. The ED-5Q and a PCC-symptom specific questionnaire were completed by the participants at 5 visits during the 20-week study period. The primary endpoint was the change in the number and/or severity of PCC-related symptoms after the 6-week intervention compared to placebo. Participants who completed the two-dosing period were included in the primary analysis, while all participants receiving one dose were included in safety assessment.

FINDINGS

From May 25th, 2021, to September 22nd, 2021, 121 participants underwent randomization, and 119 completed both dosing periods - 59 and 60 in group A and B, respectively. At baseline, the mean PCC-related symptom score was 43.06 (95% CI: 40.18; 45.94), and the mean EQ-5D health index was 0.66 (95% CI: 0.64; 0.68). The difference between CoQ10 and placebo was not significant with respect to either the change in EQ-5D health index (with a mean difference of 0.01; 95% CI: -0.02; 0.04;  = 0.45) or the change in PCC-related symptom score (with a mean difference of -1.18; 95% CI: -3.54; 1.17;  = 0.32).

INTERPRETATION

Based on self-reported data, CoQ10 treatment does not appear to significantly reduce the number or severity of PCC-related symptoms when compared to placebo. However, we observed a significant spontaneous improvement on both scores regardless of treatment during 20 weeks observation.

FUNDING

Placebo and CoQ10 capsules were provided by Pharma Nord, and the trial was supported by grants from the Novo Nordisk Foundation (NNF21OC0066984). This trial is registered with EudraCT, 2020-005961-16 and ClinicalTrials.gov, NCT04960215. The trial is completed.

摘要

背景

新冠后状况(PCC)被定义为新冠病毒感染(COVID-19)后持续超过12周的症状。在从COVID-19患者获取的外周血单核细胞中已报告有线粒体功能障碍的证据。我们推测PCC是由长期线粒体功能障碍引起的。鉴于辅酶Q10(CoQ10)可改善线粒体功能,我们研究了高剂量CoQ10是否能减少PCC相关症状的数量和/或严重程度。

方法

在这项安慰剂对照、双盲、2×2交叉干预试验中,参与者从丹麦奥胡斯大学医院和戈德斯特鲁普医院的两个中心招募。他们被随机分配接受每日剂量为500毫克的CoQ10口服胶囊或安慰剂,为期6周,在4周的洗脱期后进行交叉治疗。在为期20周的研究期间,参与者在5次访视时完成了欧洲五维度健康量表(ED-5Q)和一份PCC症状特异性问卷。主要终点是与安慰剂相比,6周干预后PCC相关症状的数量和/或严重程度的变化。完成两个给药期的参与者纳入主要分析,而所有接受一剂的参与者纳入安全性评估。

研究结果

从2021年5月25日至2021年9月22日,121名参与者接受了随机分组,119名完成了两个给药期,A组和B组分别为59名和60名。基线时,PCC相关症状的平均评分为43.06(95%置信区间:40.18;45.94),平均EQ-5D健康指数为0.66(95%置信区间:0.64;0.68)。CoQ10与安慰剂在EQ-5D健康指数变化方面(平均差异为0.01;95%置信区间:-0.02;0.04;P=0.45)或PCC相关症状评分变化方面(平均差异为-1.18;95%置信区间:-3.54;1.17;P=0.32)均无显著差异。

解读

基于自我报告数据,与安慰剂相比,CoQ10治疗似乎并未显著减少PCC相关症状的数量或严重程度。然而,在20周的观察期内,无论治疗如何,我们观察到两个评分均有显著的自发改善。

资金来源

安慰剂和CoQ10胶囊由北欧制药公司提供,该试验由诺和诺德基金会(NNF21OC0066984)的资助支持。本试验已在欧洲临床试验数据库(EudraCT)注册,注册号为2020-005961-16,在美国国立医学图书馆临床试验注册库(ClinicalTrials.gov)注册,注册号为NCT04960215。该试验已完成。

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