Results of Open-Label non-Randomized Comparative Clinical Trial: “BromhexIne and Spironolactone for CoronаvirUs Infection requiring hospiTalization (BISCUIT)
https://doi.org/10.18087/cardio.2020.11.n1440
Abstract
Introduction The aim of this study was to assess the efficacy and safety of a combination of bromhexine at a dose of 8 mg 4 times a day and spironolactone 50 mg per day in patients with mild and moderate COVID 19.
Material and methods It was an open, prospective comparative non-randomized study. 103 patients were included (33 in the bromhexine and spironolactone group and 70 in the control group). All patients had a confirmed 2019 novel coronavirus infection (COVID 19) based on a positive polymerase chain reaction (PCR) for SARS-CoV-2 virus RNA and/or a typical pattern of viral pneumonia on multispiral computed tomography. The severity of lung damage was limited to stage I-II, the level of CRP should not exceed 60 mg / dL and SO2 in the air within 92-98%. The duration of treatment is 10 days.
Results The decrease in scores on the SHOKS-COVID scale, which, in addition to assessing the clinical status, the dynamics of CRP (a marker of inflammation), D-dimer (a marker of thrombus formation), and the degree of lung damage on CT (primary endpoint) was statistically significant in both groups and differences between them was not identified. Analysis for the group as a whole revealed a statistically significant reduction in hospitalization time from 10.4 to 9.0 days (by 1.5 days, p=0.033) and fever time from 6.5 to 3.9 days (by 2.5 days, p<0.001). Given the incomplete balance of the groups, the main analysis included 66 patients who were match with using propensity score matching. In matched patients, temperature normalization in the bromhexine/spironolactone group occurred 2 days faster than in the control group (p=0.008). Virus elimination by the 10th day was recorded in all patients in the bromhexine/spironolactone group; the control group viremia continued in 23.3% (p=0.077). The number of patients who had a positive PCR to the SARS-CoV-2 virus on the 10th day of hospitalization or longer (≥10 days) hospitalization in the control group was 20/21 (95.2%), and in the group with bromhexine /spironolactone -14/24 (58.3%), p=0.012. The odds ratio of having a positive PCR or more than ten days of hospitalization was 0.07 (95% CI: 0.008 - 0.61, p=0.0161) with bromhexine and spironolactone versus controls. No side effects were reported in the study group.
Conclusion The combination of bromhexine with spironolactone appeared effective in treating a new coronavirus infection by achieving a faster normalization of the clinical condition, lowering the temperature one and a half times faster, and reducing explanatory combine endpoint the viral load or long duration of hospitalization (≥ 10 days).
About the Authors
V. Yu. MareevRussian Federation
Chief Researcher Medical Research and Education Center of Moscow State University M.V. Lomonosova, Moscow, Russia
Ya. A. Orlova
Russian Federation
Head of the Department of Age-Associated Diseases Medical Research Center of Moscow State University M.V. Lomonosova
A. G. Plisyk
Russian Federation
Senior Researcher
E. P. Pavlikova
Russian Federation
Deputy Director Clinical Work, Chief Physician Medical Research and Education Center of Moscow State University M.V. Lomonosova
S. T. Matskeplishvili
Russian Federation
Deputy Director for Research, Cardiologist Medical Research and Education Center of Moscow State University M.V. Lomonosova
Z. A. Akopyan
Russian Federation
Deputy Director of the Moscow State University
E. M. Seredenina
Russian Federation
Head of the Department of Therapy, Senior Researcher
A. V. Potapenko
Russian Federation
Head of the Admissions Department, Senior Researcher
M. A. Agapov
Russian Federation
Head of the Surgery department
D. A. Asratyan
Russian Federation
Head of the Department of Traumatology, Associate Professor
L. I. Dyachuk
Russian Federation
Head of Cardiology departmеnt
L. M. Samokhodskaya
Russian Federation
Head of the Laboratory Diagnostics Department Medical Research and Education Center of Moscow State University M.V. Lomonosova
Е. А. Mershina
Russian Federation
Head Department of X-ray diagnostics, CT and MRI, radiologist Medical Scientific and Educational Center of Moscow State University M.V. Lomonosova
V. E. Sinitsyn
Russian Federation
Head of the Department of Radiation Diagnostics Medical Research and Educational Center of Moscow State University M.V. Lomonosova
P. V. Pakhomov
Russian Federation
CLINICAL ORDINATOR
M. M. Bulanova
Russian Federation
student
A. A. Fuks
Russian Federation
student
Yu. V. Mareev
Russian Federation
Senior Researcher
Yu. L. Begrambekova
Russian Federation
Leading Researcher Medical Research and Education Center of Moscow State University M.V. Lomonosova
А. А. Kamalov
Russian Federation
Director Medical Research and Educational Center of Moscow State University M.V. Lomonosova
References
1. Cao B, Wang Y, Wen D, Liu W, Wang J, Fan G et al. A Trial of Lopinavir–Ritonavir in Adults Hospitalized with Severe Covid-19. New England Journal of Medicine. 2020;382(19):1787–99. DOI: 10.1056/NEJMoa2001282
2. Horby PW, Mafham M, Bell JL, Linsell L, Staplin N, Emberson J et al. Lopinavir–ritonavir in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform tr al. The Lancet. 2020;396(10259):1345–52. DOI: 10.1016/S0140-6736(20)32013-4
3. Beigel JH, Tomashek KM, Dodd LE, Mehta AK, Zingman BS, Kalil AC et al. Remdesivir for the Treatment of Covid-19 — Preliminary Report. New England Journal of Medicine. 2020;NEJMoa2007764. [Epub ahead of print]. DOI: 10.1056/NEJMoa2007764
4. Wang Y, Zhang D, Du G, Du R, Zhao J, Jin Y et al. Remdesivir in adults with severe COVID-19: a randomised, double-blind, placebo-controlled, multicentre trial. The Lancet. 2020;395(10236):1569–78. DOI: 10.1016/S0140-6736(20)31022-9
5. Adamsick ML, Gandhi RG, Bidell MR, Elshaboury RH, Bhattacharyya RP, Kim AY et al. Remdesivir in Patients with Acute or Chronic Kidney Disease and COVID-19. Journal of the American Society of Nephrology. 2020;31(7):1384–6. DOI: 10.1681/ASN.2020050589
6. Fan Q, Zhang B, Ma J, Zhang S. Safety profile of the antiviral drug remdesivir: An update. Biomedicine & Pharmacotherapy. 2020;130:110532. DOI: 10.1016/j.biopha.2020.110532
7. Pharmaceutical technology. Fujifilm to seek approval for Avigan in Covid-19 after positive data. 23 September 2020. [Internet] Available at: https://www.pharmaceutical-technology.com/news/fujifilm-avigan-covid-data/#:~:text=Japan’s%20Fujifilm%20Toyama%20Chemical%20plans,in%20Japan%20to%20treat%20influenza
8. Medvestnik. RDIF announced the first results of the Favipiravir study for COVID-19 in Russia. 14.05.2020. Available at: https://medvestnik.ru/content/news/Bolee-polovinyprinimavshih-Favipiravir-uchastnikov-issledovanii-izlechilis-ot-koronavirusa.html
9. Ministry of Health of Russian Federation. Temporary methodical recommendations. Prevention, diagnosis and treatment of new coronavirus infection (COVID-2019). Version 9 (26.10.2020).
10. Av. at: https://static-.minzdrav.gov.ru/system/attachments/attaches/000/052/548/original/%D0%9C%D0%A0_COVID19_%28v.9%29.pdf?1603730062.
11. Mareev V.Yu., Orlova Ya.A., Pavlikova E.P., Matskeplishvili S.T., Krasnova T.N., Malahov P.S. et al. Steroid pulse-therapy in patients With coronAvirus Pneumonia (COVID-19), sYstemic inFlammation And Risk of vEnous thRombosis and thromboembolism (WAYFARER Study). Kardiologiia. 2020;60(6):15–29. DOI: 10.18087/cardio.2020.6.n1226
12. Sonawane K, Barale SS, Dhanavade MJ, Waghmare SR, Nadaf NH, Kamble SA et al. Homology Modeling and Docking Studies of TMPRSS2 with Experimentally Known Inhibitors Camostat Mesylate, Nafamostat and Bromhexine Hydrochloride to Control SARS-Coronavirus-2. 2020. [Av. at: https://chemrxiv.org/articles/Homology_Modeling_and_Docking_Studies_of_TMPRSS2_with_Experimentally_Known_Inhibitors_Camostat_Mesylate_Nafamostat_and_Bromhexine_Hydrochloride_to_Control_SARS-Coronavirus-2/12162360/1].
13. Zanasi A, Mazzolini M, Kantar A. A reappraisal of the mucoactive activity and clinical efficacy of bromhexine. Multidisciplinary Respiratory Medicine. 2017;12(1):7. DOI: 10.1186/s40248-017-0088-1
14. Ji W-J, Ma Y-Q, Zhou X, Zhang Y-D, Lu R-Y, Guo Z-Z et al. Spironolactone Attenuates Bleomycin-Induced Pulmonary Injury Partially via Modulating Mononuclear Phagocyte Phenotype Switching in Circulating and Alveolar Compartments. PLoS ONE. 2013;8(11):e81090. DOI: 10.1371/journal.pone.0081090
15. Wambier CG, Goren A, Ossimetha A, Nau G, Qureshi AA. Androgen-driven COVID-19 pandemic theory. ResearchGate. 2020; DOI: 10.13140/RG.2.2.21254.11848
16. Goren A, Vaño‐Galván S, Wambier CG, McCoy J, Gomez‐Zubiaur A, Moreno‐Arrones OM et al. A preliminary observation: Male pattern hair loss among hospitalized COVID‐19 patients in Spain – A potential clue to the role of androgens in COVID‐19 severity. Journal of Cosmetic Dermatology. 2020;19(7):1545–7. DOI: 10.1111/jocd.13443
17. Asselta R, Paraboschi EM, Mantovani A, Duga S. ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy. 2020. [Av. at: http://medrxiv.org/lookup/doi/10.1101/2020.03.30.20047878].
18. Mareev V.Yu., Orlova Ya.A., Pavlikova E.P., Matskeplishvili S.T., Akopyan Zh.A., Plisyk A.G. et al. Combination therapy at an early stage of the novel coronavirus infection (COVID-19). Case series and design of the clinical trial “BromhexIne and Spironolactone for CoronаvirUs Infection requiring hospiTalization (BISCUIT)”. Kardiologiia. 2020;60(8):4–15. DOI: 10.18087/cardio.2020.8.n1307
19. Lomonosov Moscow State University Medical Research and Educational Center. Open Label Randomized Clinical Trial BromhexIne And Spironolactone For CoronаVirUs Infection Requiring HospiTalization. ClinicalTrials.gov Identifier: NCT04424134. 2020. [Av. at: https://clinicaltrials.gov/ct2/show/NCT04424134].
20. Royal College of Physicians. National Early Warning Score (NEWS) 2. [Av. at: https://www.rcplondon.ac.uk/projects/outputs/national-early-warning-score-news-2]. 2017.
21. Liao X, Wang B, Kang Y. Novel coronavirus infection during the 2019–2020 epidemic: preparing intensive care units—the experience in Sichuan Province, China. Intensive Care Medicine. 2020;46(2):357–60. DOI: 10.1007/s00134-020-05954-2
22. Spinner CD, Gottlieb RL, Criner GJ, Arribas López JR, Cattelan AM, Soriano Viladomiu A et al. Effect of Remdesivir vs Standard Care on Clinical Status at 11 Days in Patients With Moderate COVID-19: A Randomized Clinical Trial. JAMA. 2020;324(11):1048. DOI: 10.1001/jama.2020.16349
23. Geleris J, Sun Y, Platt J, Zucker J, Baldwin M, Hripcsak G et al. Observational Study of Hydroxychloroquine in Hospitalized Patients with Covid-19. New England Journal of Medicine. 2020;382(25):2411–8. DOI: 10.1056/NEJMoa2012410
24. Horby P, Mafham M, Linsell L, Bell JL, Staplin N, Emberson JR et al. Effect of Hydroxychloroquine in Hospitalized Patients with COVID-19: Preliminary results from a multi-centre, randomized, controlled trial. 2020. [Av. at: http://medrxiv.org/lookup/doi/10.1101/2020.07.15.20151852].
25. WHO Solidarity trial consortium, Pan H, Peto R, Karim QA, Alejandria M, Henao-Restrepo AM et al. Repurposed antiviral drugs for COVID-19 –interim WHO SOLIDARITY trial results. [Av. at: http://medrxiv.org/lookup/doi/10.1101/2020.10.15.20209817]. 2020.
26. Sanders JM, Monogue ML, Jodlowski TZ, Cutrell JB. Pharmacologic Treatments for Coronavirus Disease 2019 (COVID- 19): A Review. JAMA. 2020;323(18):1824–36. DOI: 10.1001/jama.2020.6019
27. Cai Q, Yang M, Liu D, Chen J, Shu D, Xia J et al. Experimental Treatment with Favipiravir for COVID-19: An Open-Label Control Study. Engineering. 2020; [Epub ahead of print]. DOI: 10.1016/j.eng.2020.03.007
28. Hung IF-N, Lung K-C, Tso EY-K, Liu R, Chung TW-H, Chu M-Y et al. Triple combination of interferon beta-1b, lopinavir–ritonavir, and ribavirin in the treatment of patients admitted to hospital with COVID-19: an open-label, randomised, phase 2 trial. The Lancet. 2020;395(10238):1695–704. DOI: 10.1016/S0140-6736(20)31042-4
29. Shen LW, Mao HJ, Wu YL, Tanaka Y, Zhang W. TMPRSS2: A potential target for treatment of influenza virus and coronavirus infections. Biochimie. 2017;142:1–10. DOI: 10.1016/j.biochi.2017.07.016
30. Olaleye OA, Kaur M, Onyenaka CC. Ambroxol Hydrochloride Inhibits the Interaction between Severe Acute Respiratory Syndrome Coronavirus 2 Spike Protein’s Receptor Binding Domain and Recombinant Human ACE2. [Av. at: http://biorxiv.org/lookup/doi/10.1101/2020.09.13.295691]. 2020.
31. Ansarin K, Tolouian R, Ardalan M, Taghizadieh A, Varshochi M, Teimouri S et al. Effect of bromhexine on clinical outcomes and mortality in COVID-19 patients: A randomized clinical trial. BioImpacts. 2020;10(4):209–15. DOI: 10.34172/bi.2020.27
32. Yavas G, Yavas C, Celik E, Sen E, Ata O, Afsar RE. The impact of spironolactone on the lung injury induced by concomitant trastuzumab and thoracic radiotherapy. International Journal of Radiation Research. 2019;17(1):87–95. [Av. at: http://ijrr.com/article1-2461-en.html]
33. Chen D, Li X, Song Q, Hu C, Su F, Dai J et al. Assessment of Hypokalemia and Clinical Characteristics in Patients With Coronavirus Disease 2019 in Wenzhou, China. JAMA Network Open. 2020;3(6):e2011122. DOI: 10.1001/jamanetworkopen.2020.11122
34. Juurlink DN, Mamdani MM, Lee DS, Kopp A, Austin PC, Laupacis A et al. Rates of Hyperkalemia after Publication of the Randomized Aldactone Evaluation Study. New England Journal of Medicine. 2004;351(6):543–51. DOI: 10.1056/NEJMoa040135
35. The Human Protein Atlas. Tissue expression of ADAM17. [Internet] Available at: https://www.proteinatlas.org/ENSG00000151694-ADAM17/tissue
36. Lin B, Ferguson C, White JT, Wang S, Vessella R, True LD et al. Prostate-localized and androgen-regulated expression of the membrane-bound serine protease TMPRSS2. Cancer Research. 1999;59(17):4180–4. PMID: 10485450
37. Mikkonen L, Pihlajamaa P, Sahu B, Zhang F-P, Jänne OA. Androgen receptor and androgen-dependent gene expression in lung. Molecular and Cellular Endocrinology. 2010;317(1–2):14–24. DOI: 10.1016/j.mce.2009.12.022
38. Montopoli M, Zumerle S, Vettor R, Rugge M, Zorzi M, Catapano V et al. Androgen-deprivation therapies for prostate cancer and risk of infection by SARS-CoV-2: a population-based study (N = 4532). Annals of Oncology. 2020;31(8):1040–5. DOI: 10.1016/j.annonc.2020.04.479
39. Loriaux DL. Spironolactone and Endocrine Dysfunction. Annals of Internal Medicine. 1976;85(5):630. DOI: 10.7326/0003-4819-85-5-630
40. McMullen GR, Van Herle AJ. Hirsutism and the effectiveness of spironolactone in its management. Journal of Endocrinological Investigation. 1993;16(11):925–32. DOI: 10.1007/BF03348960
41. Liaudet L, Szabo C. Blocking mineralocorticoid receptor with spironolactone may have a wide range of therapeutic actions in severe COVID-19 disease. Critical Care. 2020;24(1):318. DOI: 10.1186/s13054-020-03055-6
42. Flávio C, Wambier C, Goren A. Spironolactone protection for SARSCoV-2: Targeting androgens and angiotensin converting enzyme 2 (ACE2). ResearchGate. 2020; [Av. at: https://www.researchgate.net/publication/341103985]
Review
For citations:
Mareev V.Yu., Orlova Ya.A., Plisyk A.G., Pavlikova E.P., Matskeplishvili S.T., Akopyan Z.A., Seredenina E.M., Potapenko A.V., Agapov M.A., Asratyan D.A., Dyachuk L.I., Samokhodskaya L.M., Mershina Е.А., Sinitsyn V.E., Pakhomov P.V., Bulanova M.M., Fuks A.A., Mareev Yu.V., Begrambekova Yu.L., Kamalov А.А. Results of Open-Label non-Randomized Comparative Clinical Trial: “BromhexIne and Spironolactone for CoronаvirUs Infection requiring hospiTalization (BISCUIT). Kardiologiia. 2020;60(11):4-15. https://doi.org/10.18087/cardio.2020.11.n1440