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Diacerein reduces inflammasome activation and SARS-CoV-2 virus replication: a proof-of-concept translational study

Carmo et al., Frontiers in Pharmacology, doi:10.3389/fphar.2024.1402032, NCT05226754, Oct 2024
https://c19early.org/carmo.html
Hospitalization time -10% improvement lower risk ← → higher risk Diacerein  Carmo et al.  LATE TREATMENT RCT Is late treatment with diacerein beneficial for COVID-19? Double-blind RCT 14 patients in Brazil (April - December 2022) No significant difference in hospitalization c19early.org Carmo et al., Frontiers in Pharmacology, Oct 2024 0 0.5 1 1.5 2+ RR
RCT 14 hospitalized patients with mild to moderate COVID-19 showing reduced plasma inflammasome markers with diacerein treatment, but no significant difference in duration of hospitalization. The study was halted early due to declining COVID-19 hospitalizations, limiting statistical power.
hospitalization time, 9.9% higher, relative time 1.10, p = 0.79, treatment mean 7.8 (±4.9) n=7, control mean 7.1 (±4.7) n=7.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Carmo et al., 7 Oct 2024, Double Blind Randomized Controlled Trial, placebo-controlled, Brazil, peer-reviewed, median age 62.0, 28 authors, study period 6 April, 2022 - 14 December, 2022, trial NCT05226754 (history). Contact: sposito@unicamp.br.
$0 $500 $1,000+ Efficacy vs. cost for COVID-19 treatment protocols c19early.org November 2025 Brazil United Kingdom Russia Sudan Angola Colombia Kenya Mozambique Vietnam Peru Philippines China Uzbekistan Nepal Ethiopia Iran Ghana Mexico South Korea Germany Bangladesh Saudi Arabia Algeria Morocco Yemen Poland India DR Congo Madagascar Thailand Uganda Venezuela Nigeria Egypt Bolivia Taiwan Zambia Fiji Bosnia-Herzegovina Ukraine Côte d'Ivoire Bulgaria Greece Slovakia Singapore Iceland New Zealand Czechia Mongolia Israel Trinidad and Tobago Hong Kong North Macedonia Belarus Qatar Panama Serbia CAR Brazil favored high-profit treatments.The average efficacy of treatments was very low.High-cost protocols reduce early treatment, andforgo complementary/synergistic benefits. More effective More expensive 75% 50% 25% ≤0%
$0 $500 $1,000+ Efficacy vs. cost for COVID-19treatment protocols worldwide c19early.org November 2025 Brazil United Kingdom Russia USA Sudan Angola Colombia Kenya Mozambique Vietnam Peru Philippines China Uzbekistan Nepal Ethiopia Iran Ghana Mexico South Korea Germany Bangladesh Saudi Arabia Algeria Morocco Yemen Poland India DR Congo Madagascar Thailand Uganda Venezuela Nigeria Egypt Bolivia Taiwan Zambia Fiji Bosnia-Herzegovina Ukraine Côte d'Ivoire Eritrea Bulgaria Greece Slovakia Singapore New Zealand Malawi Czechia Mongolia Israel Trinidad and Tobago North Macedonia Belarus Qatar Panama Serbia Syria Brazil favored high-profit treatments.The average efficacy was very low.High-cost protocols reduce early treatment,and forgo complementary/synergistic benefits. More effective More expensive 75% 50% 25% ≤0%
Diacerein reduces inflammasome activation and SARS-CoV-2 virus replication: a proof-of-concept translational study
Helison R P Carmo, Alejandro Rossel Castillo, Isabella Bonilha, Erica I L Gomes, Joaquim Barreto, Filipe A Moura, Gustavo Gastão Davanzo, Lauar De Brito Monteiro, Stéfanie Primon Muraro, Gabriela Fabiano De Souza, Joseane Morari, Flávia Elisa Galdino, Natália S Brunetti, Guilherme Reis-De-Oliveira, Victor Corasolla Carregari, Wilson Nadruz, Daniel Martins-De-Souza, Alessandro S Farias, Licio A Velloso, José Luiz Proenca-Modena, Marcelo A Mori, Watson Loh, Deepak L Bhatt, Derek M Yellon, Sean M Davidson, Pedro G De Oliveira, Pedro M Moraes-Vieira, Andrei C Sposito
Frontiers in Pharmacology, doi:10.3389/fphar.2024.1402032
Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is linked to high mortality, primarily through an intense inflammatory response. Diacerein has emerged as a potential therapy for COVID-19 due to its potential impact in decreasing the inflammasome activation and coronavirus replication. This study aims to explore diacerein's influence in inhibiting both viral replication and the inflammatory response after SARS-CoV-2 infection.
Conflict of interest Amgen, AstraZeneca, Bayer, Beren, Boehringer Ingelheim, Boston Scientific, Bristol-Myers Squibb, Cardax, CellProthera, Cereno Scientific, Chiesi, CinCor, Cleerly, CSL Behring, Eisai, Ethicon, Faraday Pharmaceuticals, Ferring Pharmaceuticals, Forest Laboratories, Fractyl, Garmin, HLS Therapeutics, Idorsia, Ironwood, Ischemix, Janssen, Javelin, Lexicon, Lilly, Medtronic, Merck, Moderna, MyoKardia, NirvaMed, Novartis, Novo (FAPESP) . Dr. Pedro Gonç alves de Oliveira is responsible for R&D activities at TRB Pharma Indú stria Quí mica e Farmace utica Ltda, SP, Brazil. TRB Pharma is the owner of the product ARTRODAR ® a diacerein-based product for osteoarthritis treatment. The remaining 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/fphar.2024.1402032/ full#supplementary-material
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DOI record: { "DOI": "10.3389/fphar.2024.1402032", "ISSN": [ "1663-9812" ], "URL": "http://dx.doi.org/10.3389/fphar.2024.1402032", "abstract": "<jats:sec><jats:title>Background</jats:title><jats:p>Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is linked to high mortality, primarily through an intense inflammatory response. Diacerein has emerged as a potential therapy for COVID-19 due to its potential impact in decreasing the inflammasome activation and coronavirus replication. This study aims to explore diacerein’s influence in inhibiting both viral replication and the inflammatory response after SARS-CoV-2 infection.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Human peripheral blood mononuclear cells (PBMCs) were obtained from healthy volunteers and infected <jats:italic>in vitro</jats:italic> with SARS-CoV-2. Additionally, we carried out a pilot randomized, double-blind, placebo-controlled study with 14 participants allocated to diacerein (n = 7) or placebo (n = 7) therapies every 12 h for 10 days. The primary endpoint was change in plasma markers of inflammasome activation (NLRP3, caspase-1, and gasdermin-D).</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p><jats:italic>In vitro</jats:italic> protocols have shown that rhein, diacerein’s primary metabolite, decreased IL-1β secretion caused by SARS-CoV-2 infection in human PBMCs (<jats:italic>p</jats:italic> &amp;lt; 0.05), and suppressed viral replication when administered either before or after the virus incubation (<jats:italic>p</jats:italic> &amp;lt; 0.05). This later effect was, at least partially, attributed to its inhibitory effect on 3-chymotrypsin-like protease (SARS-CoV-2 3CL<jats:sup>pro</jats:sup>) and papain-like protease in the SARS-CoV-2 (SARS-CoV-2 PL<jats:sup>pro</jats:sup>) virus and in the phosphorylation of proteins related cytoskeleton network (<jats:italic>p</jats:italic> &amp;lt; 0.05). Diacerein-treated COVID-19 patients presented a smaller area under the curve for NLRP3, caspase-1 and GSDM-D measured on days 2, 5, and 10 after hospitalization compared to those receiving a placebo (<jats:italic>p</jats:italic> &amp;lt; 0.05).</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>The indicated mechanisms of action of diacerein/rhein can reduce viral replication and mitigate the inflammatory response related to SARS-CoV-2. These findings are preliminary and require confirmation in clinical trials.</jats:p></jats:sec>", "alternative-id": [ "10.3389/fphar.2024.1402032" ], "author": [ { "affiliation": [], "family": "Carmo", "given": "Helison R. P.", "sequence": "first" }, { "affiliation": [], "family": "Castillo", "given": "Alejandro Rossel", "sequence": "additional" }, { "affiliation": [], "family": "Bonilha", "given": "Isabella", "sequence": "additional" }, { "affiliation": [], "family": "Gomes", "given": "Erica I. L.", "sequence": "additional" }, { "affiliation": [], "family": "Barreto", "given": "Joaquim", "sequence": "additional" }, { "affiliation": [], "family": "Moura", "given": "Filipe A.", "sequence": "additional" }, { "affiliation": [], "family": "Davanzo", "given": "Gustavo Gastão", "sequence": "additional" }, { "affiliation": [], "family": "de Brito Monteiro", "given": "Lauar", "sequence": "additional" }, { "affiliation": [], "family": "Muraro", "given": "Stéfanie Primon", "sequence": "additional" }, { "affiliation": [], "family": "Fabiano de Souza", "given": "Gabriela", "sequence": "additional" }, { "affiliation": [], "family": "Morari", "given": "Joseane", "sequence": "additional" }, { "affiliation": [], "family": "Galdino", "given": "Flávia Elisa", "sequence": "additional" }, { "affiliation": [], "family": "Brunetti", "given": "Natália S.", "sequence": "additional" }, { "affiliation": [], "family": "Reis-de-Oliveira", "given": "Guilherme", "sequence": "additional" }, { "affiliation": [], "family": "Carregari", "given": "Victor Corasolla", "sequence": "additional" }, { "affiliation": [], "family": "Nadruz", "given": "Wilson", "sequence": "additional" }, { "affiliation": [], "family": "Martins-de-Souza", "given": "Daniel", "sequence": "additional" }, { "affiliation": [], "family": "Farias", "given": "Alessandro S.", "sequence": "additional" }, { "affiliation": [], "family": "Velloso", "given": "Licio A.", "sequence": "additional" }, { "affiliation": [], "family": "Proenca-Modena", "given": "José Luiz", "sequence": "additional" }, { "affiliation": [], "family": "Mori", "given": "Marcelo A.", "sequence": "additional" }, { "affiliation": [], "family": "Loh", "given": "Watson", "sequence": "additional" }, { "affiliation": [], "family": "Bhatt", "given": "Deepak L.", "sequence": "additional" }, { "affiliation": [], "family": "Yellon", "given": "Derek M.", "sequence": "additional" }, { "affiliation": [], "family": "Davidson", "given": "Sean M.", "sequence": "additional" }, { "affiliation": [], "family": "De Oliveira", "given": "Pedro G.", "sequence": "additional" }, { "affiliation": [], "family": "Moraes-Vieira", "given": "Pedro M.", "sequence": "additional" }, { "affiliation": [], "family": "Sposito", "given": "Andrei C.", "sequence": "additional" } ], "container-title": "Frontiers in Pharmacology", "container-title-short": "Front. 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Late treatment
is less effective
Please send us corrections, updates, or comments. c19early involves the extraction of 200,000+ datapoints from thousands of papers. Community updates help ensure high accuracy. Treatments and other interventions are complementary. All practical, effective, and safe means should be used based on risk/benefit analysis. No treatment or intervention is 100% available and effective for all current and future variants. We do not provide medical advice. Before taking any medication, consult a qualified physician who can provide personalized advice and details of risks and benefits based on your medical history and situation. IMA and WCH provide treatment protocols.
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