Effect of spirulina on risk of hospitalization among patients with COVID-19: the TOGETHER randomized trial

被引:1
|
作者
Reis, Gilmar [1 ,2 ,3 ]
Silva, Eduardo Augusto dos Santos Moreira [1 ,2 ]
Silva, Daniela Carla Medeiros [1 ,2 ]
Thabane, Lehana [3 ]
Ferreira, Thiago Santiago [1 ]
dos Santos, Castilho Vitor Quirino [1 ,2 ]
Almeida, Ana Paula Figueiredo Guimaraes [6 ]
Savassi, Leonardo Cancado Monteiro [4 ]
Neto, Adhemar Dias de Figueiredo [7 ]
Reis, Luiza Lanna Franca [1 ,2 ]
Campos, Vitoria Helena de Souza [2 ]
Bitaraes, Carina [4 ,5 ]
Callegari, Eduardo Diniz [8 ]
Simplicio, Maria Izabel Campos [1 ]
Ribeiro, Luciene Barra [1 ]
Oliveira, Rosemary [1 ]
Harari, Ofir [9 ]
Forrest, Jamie [9 ]
Lat, Prince Kumar [9 ]
Dron, Louis [10 ]
Thorlund, Kristian [3 ]
Mills, Edward [9 ]
机构
[1] Cardresearch Cardiol Assistencial & Pesquisa, Res Div, Belo Horizonte, MG, Brazil
[2] Pontif Univ Catolica Minas Gerais, Dept Med, Fac Med, Belo Horizonte, MG, Brazil
[3] McMaster Univ, Dept Hlth Res Methods Evidence & Impact, Hamilton, ON, Canada
[4] Univ Fed Ouro Preto, Mental & Family Med Dept, Publ Hlth, Ouro Preto, MG, Brazil
[5] Publ Hlth Care Div, City Ibirite, Ibirite, MG, Brazil
[6] Dept Publ Hlth UniFipMoc, Family Med Fellowship Program, Montes Claros, MG, Brazil
[7] Governador Valadares Publ Hlth Author, Publ Hlth Fellowship Program, Valadares, MG, Brazil
[8] Publ Hlth Care Div, Brumadinho, MG, Brazil
[9] Purpose Life Sci, Vancouver, BC, Canada
[10] Cascade Outcomes Res, Vancouver, BC, Canada
关键词
Brazil; SARS-CoV-2; repurposed drugs; outpatients; spirulina;
D O I
10.1016/j.ajcnut.2024.06.016
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Algae-derived nutraceuticals, such as spirulina, have been reported to have biological activities that may minimize clinical consequences to COVID-19 infections. Objectives: This study aimed to determine whether spirulina is an effective treatment for high-risk patients with early COVID-19 in an outpatient setting. Methods: The TOGETHER trial is a placebo-controlled, randomized, platform trial conducted in Brazil. Eligible participants were symptomatic adults with a positive rapid test for SARS-CoV-2 older than 50 y or with a known risk factor for disease severity. Patients were randomly assigned to receive placebo or spirulina (1 g twice daily for 14 d). The primary end point was hospitalization defined as either retention in a COVID-19 emergency setting for >6 h or transfer to tertiary hospital owing to COVID-19 at 28 d. Secondary outcomes included time-to-hospitalization, mortality, and adverse drug reactions. We used a Bayesian framework to compare spirulina with placebo. Results: We recruited 1126 participants, 569 randomly assigned to spirulina and 557 to placebo. The median age was 49.0 y, and 65.3% were female. The primary outcome occurred in 11.2% in the spirulina group and 8.1% in the placebo group (odds ratio [OR]: 1.24; 95% credible interval: 0.84, 1.86). There were no differences in emergency department visit (OR: 1.21; 95% credible interval: 0.81, 1.83), nor time to symptom relief (hazard ratio: 0.90; 95% credible interval: 0.79, 1.03). Spirulina also not demonstrate important treatment effects in the prespecified subgroups defined by age, sex, BMI, days since symptom onset, or vaccination status. Conclusions: Spirulina has no any clinical benefits as an outpatient therapy for COVID-19 compared with placebo with respect to reducing the retention in an emergency setting or COVID-19-related hospitalization. There are no differences between spirulina and placebo for other secondary outcomes.
引用
收藏
页码:602 / 609
页数:8
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