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0 0.5 1 1.5 2+ Mortality, combined 85% Improvement Relative Risk Mortality, Non-ICU 87% Mortality, ICU 84% Discharge, combined 75% Discharge, Non-ICU 85% Discharge, ICU 61% Spirulina  Aghasadeghi et al.  LATE TREATMENT  RCT Is late treatment with spirulina beneficial for COVID-19? RCT 189 patients in Iran (June 2021 - February 2022) Lower mortality (p=0.00017) and higher discharge (p=0.0026) c19early.org Aghasadeghi et al., Frontiers in Immun.., Apr 2024 Favors spirulina Favors control

Effect of high-dose Spirulina supplementation on hospitalized adults with COVID-19: a randomized controlled trial

Aghasadeghi et al., Frontiers in Immunology, doi:10.3389/fimmu.2024.1332425, IRCT20210216050373N1
Apr 2024  
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RCT 189 hospitalized COVID-19 patients showing lower mortality and faster recovery with high-dose spirulina. Spirulina treatment also resulted in greater reductions in inflammatory markers such as IL-6, TNF-a, IP-10, CRP, ESR, and ferritin. All patients received remdesivir. Spirulina contains many components including calcium spirulan, a sulfated polysaccharide shown to inhibit the replication of various enveloped viruses in vitro, and many nutrients showing benefits for COVID-19 including vitamins A, C, and D, selenium, and zinc.
risk of death, 84.8% lower, HR 0.15, p < 0.001, treatment 47, control 52, combined.
risk of death, 87.0% lower, HR 0.13, p = 0.04, treatment 0 of 44 (0.0%), control 4 of 46 (8.7%), NNT 12, adjusted per study, Non-ICU, overall mortality.
risk of death, 84.0% lower, HR 0.16, p = 0.002, treatment 0 of 47 (0.0%), control 15 of 52 (28.8%), NNT 3.5, adjusted per study, ICU, overall mortality.
risk of no hospital discharge, 75.4% lower, HR 0.25, p = 0.003, treatment 47, control 52, combined.
risk of no hospital discharge, 84.8% lower, HR 0.15, p < 0.001, treatment 0 of 44 (0.0%), control 4 of 46 (8.7%), NNT 12, adjusted per study, inverted to make HR<1 favor treatment, Non-ICU, overall discharge.
risk of no hospital discharge, 61.4% lower, HR 0.39, p < 0.001, treatment 0 of 47 (0.0%), control 37 of 52 (71.2%), NNT 1.4, adjusted per study, inverted to make HR<1 favor treatment, ICU, overall discharge.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Aghasadeghi et al., 8 Apr 2024, Randomized Controlled Trial, Iran, peer-reviewed, mean age 45.8, 26 authors, study period June 2021 - February 2022, trial IRCT20210216050373N1. Contact: a_alinaghi@sina.tums.ac.ir.
This PaperMiscellaneousAll
Effect of high-dose Spirulina supplementation on hospitalized adults with COVID-19: a randomized controlled trial
Mohammad Reza Aghasadeghi, Mohammad Ali Zaheri Birgani, Saeedreza Jamalimoghadamsiyahkali, Hadiseh Hosamirudsari, Ali Moradi, Majid Jafari-Sabet, Nooshin Sadigh, Pooneh Rahimi, Rezvan Tavakoli, Mojtaba Hamidi-Fard, Golnaz Bahramali, Zohal Parmoon, Sina Arjmand Hashjin, Ghasem Mirzajani, Reza Kouhkheil, Somayeh Roshangaran, Samineh Khalaf, Mohammad Khademi Nadoushan, Ghazaleh Gholamiyan Yousef Abad, Nima Shahryarpour, Mohammad Izadi, Abolfazl Zendedel, Shayesteh Jahanfar, Omid Dadras, Seyedahmad Seyedalinaghi, Daniel Hackett
Frontiers in Immunology, doi:10.3389/fimmu.2024.1332425
Objective: Spirulina (arthrospira platensis) is a cyanobacterium proven to have anti-inflammatory, antiviral, and antioxidant effects. However, the effect of highdose Spirulina supplementation on hospitalized adults with COVID-19 is currently unclear. This study aimed to evaluate the efficacy and safety of highdose Spirulina platensis for SARS-CoV-2 infection. Study Design: We conducted a randomized, controlled, open-label trial involving 189 patients with COVID-19 who were randomly assigned in a 1:1 ratio to an experimental group that received 15.2g of Spirulina supplement plus standard treatment (44 non-intensive care unit (non-ICU) and 47 ICU), or to a control group that received standard treatment alone (46 non-ICU and 52 ICU). The study was conducted over six days. Immune mediators were monitored on days 1, 3, 5, and 7. The primary outcome of this study was mortality or hospital Frontiers in Immunology frontiersin.org 01
Ethics statement This study is a multicenter, randomized controlled trialapproved by the Research Ethics Committee of Tehran University of Medical Sciences (IR.TUMS.IKHC.REC.1399.481) and the Iranian Registry of Clinical Trials (IRCT) registry team. The s tu dy pro t oco l is re gi stered w ith IRCT u n d e r IRCT20210216050373N1, available at https://irct.ir/trial/54375. All patients gave written informed consent before starting the study. Author contributions Conflict of interest The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. Publisher's note All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher. Supplementary material The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2024.1332425/ full#supplementary-material
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Late treatment
is less effective
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