Treatment with Zinc is Associated with Reduced In-Hospital Mortality Among COVID-19 Patients: A Multi-Center Cohort Study
Jennifer A Frontera, Joseph O Rahimian, Shadi Yaghi, Mengling Liu, Ariane Lewis, Adam De Havenon, Shraddha Mainali, Joshua Huang, Erica Scher, Thomas Wisniewski, Andrea B Troxel, Sharon Meropol, Laura J Balcer, Steven L Galetta
doi:10.21203/rs.3.rs-94509/v1
Background: Zinc impairs replication of RNA viruses such as SARS-CoV-1, and may be effective against SARS-CoV-2. However, to achieve adequate intracellular zinc levels, administration with an ionophore, which increases intracellular zinc levels, may be necessary. We evaluated the impact of zinc with an ionophore (Zn+ionophore) on COVID-19 in-hospital mortality rates. Methods: A multicenter cohort study was conducted of 3,473 adult hospitalized patients with reverse-transcriptase-polymerase-chain-reaction (RT-PCR) positive SARS-CoV-2 infection admitted to four New York City hospitals between March 10 through May 20, 2020. Exclusion criteria were: death or discharge within 24h, comfort-care status, clinical trial enrollment, treatment with an IL-6 inhibitor or remdesivir. Patients who received Zn+ionophore were compared to patients who did not using multivariable time-dependent cox proportional hazards models for time to in-hospital death adjusting for confounders including age, sex, race, BMI, diabetes, week of admission, hospital location, sequential organ failure assessment (SOFA) score, intubation, acute renal failure, neurological events, treatment with corticosteroids, azithromycin or lopinavir/ritonavir and the propensity score of receiving Zn+ionophore. A sensitivity analysis was performed using a propensity score-matched cohort of patients who did or did not receive Zn+ionophore matched by age, sex and ventilator status. Results: Among 3,473 patients (median age 64, 1947 [56%] male, 522 [15%] ventilated, 545[16%] died), 1,006 (29%) received Zn+ionophore. Zn+ionophore was associated with a 24% reduced risk of in-hospital mortality (12% of those who received Zn+ionophore died versus 17% who did not; adjusted Hazard Ratio [aHR] 0.76, 95% CI 0.60-0.96, P=0.023). More patients who received Zn+ionophore were discharged home (72% Zn+ionophore vs 67% no Zn+ionophore, P=0.003) Neither Zn nor the ionophore alone were associated with decreased mortality rates. Propensity scorematched sensitivity analysis (N=1356) validated these results (Zn+ionophore aHR for mortality 0.63, 95%CI 0.44-0.91, P=0.015). There were no signi cant interactions for Zn+ionophore with other COVID-19 speci c medications. Conclusions: Zinc with an ionophore was associated with increased rates of discharge home and a 24% reduced risk of in-hospital mortality among COVID-19 patients, while neither zinc alone nor the ionophore alone reduced mortality. Further randomized trials are warranted.
Summery In this study of 3,473 hospitalized COVID-19 patients, treatment with zinc and an ionophore was associated with a 24% reduced risk of in-hospital mortality in multivariable Cox regression analysis. A sensitivity analysis in a propensity score-matched cohort supported this nding.
Figure 2 Forest plot of subgroups evaluating the impact of treatment with zinc plus an ionophore on in-hospital mortality Supplementary Files This is a list of supplementary les associated with this preprint. Click to download.
SupplementaryAppendixZincBMCID.docx
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' <jats:p><jats:bold>Background:</jats:bold> Zinc impairs replication of RNA viruses '
'such as SARS-CoV-1, and may be effective against SARS-CoV-2. However, to achieve adequate '
'intracellular zinc levels, administration with an ionophore, which increases intracellular '
'zinc levels, may be necessary. We evaluated the impact of zinc with an ionophore '
'(Zn+ionophore) on COVID-19 in-hospital mortality rates.<jats:bold>Methods: </jats:bold>A '
'multicenter cohort study was conducted of 3,473<jats:bold> </jats:bold>adult '
'hospitalized<jats:bold> </jats:bold>patients with '
'reverse-transcriptase-polymerase-chain-reaction (RT-PCR) positive SARS-CoV-2 infection '
'admitted to four New York City hospitals between March 10 through May 20, 2020. Exclusion '
'criteria were: death or discharge within 24h, comfort-care status, clinical trial enrollment, '
'treatment with an IL-6 inhibitor or remdesivir. Patients who received Zn+ionophore were '
'compared to patients who did not using multivariable time-dependent cox proportional hazards '
'models for time to in-hospital death adjusting for confounders including age, sex, race, BMI, '
'diabetes, week of admission, hospital location, sequential organ failure assessment (SOFA) '
'score, intubation, acute renal failure, neurological events, treatment with corticosteroids, '
'azithromycin or lopinavir/ritonavir and the propensity score of receiving Zn+ionophore. A '
'sensitivity analysis was performed using a propensity score-matched cohort of patients who '
'did or did not receive Zn+ionophore matched by age, sex and ventilator '
'status.<jats:bold>Results: </jats:bold>Among 3,473 patients (median age 64, 1947 [56%] male, '
'522 [15%] ventilated, 545[16%] died), 1,006 (29%) received Zn+ionophore. Zn+ionophore was '
'associated with a 24% reduced risk of in-hospital mortality (12% of those who received '
'Zn+ionophore died versus 17% who did not; adjusted Hazard Ratio [aHR] 0.76, 95% CI 0.60-0.96, '
'P=0.023). More patients who received Zn+ionophore were discharged home (72% Zn+ionophore vs '
'67% no Zn+ionophore, P=0.003) Neither Zn nor the ionophore alone were associated with '
'decreased mortality rates. Propensity score-matched sensitivity analysis (N=1356) validated '
'these results (Zn+ionophore aHR for mortality 0.63, 95%CI 0.44-0.91, P=0.015). There were no '
'significant interactions for Zn+ionophore with other COVID-19 specific '
'medications.<jats:bold>Conclusions: </jats:bold>Zinc with an ionophore was associated with '
'increased rates of discharge home and a 24% reduced risk of in-hospital mortality among '
'COVID-19 patients, while neither zinc alone nor the ionophore alone reduced mortality. '
'Further randomized trials are warranted.</jats:p>',
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