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      Pharmacogenomics and COVID-19: clinical implications of human genome interactions with repurposed drugs

      review-article
      1 , 2 ,
      The Pharmacogenomics Journal
      Nature Publishing Group UK
      Genetic association study, Drug development

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          Abstract

          The outbreak of Coronavirus disease 2019 (COVID-19) has evolved into an emergent global pandemic. Many drugs without established efficacy are being used to treat COVID-19 patients either as an offlabel/compassionate use or as a clinical trial. Although drug repurposing is an attractive approach with reduced time and cost, there is a need to make predictions on success before the start of therapy. For the optimum use of these repurposed drugs, many factors should be considered such as drug–gene or dug–drug interactions, drug toxicity, and patient co-morbidity. There is limited data on the pharmacogenomics of these agents and this may constitute an obstacle for successful COVID-19 therapy. This article reviewed the available human genome interactions with some promising repurposed drugs for COVID-19 management. These drugs include chloroquine (CQ), hydroxychloroquine (HCQ), azithromycin, lopinavir/ritonavir (LPV/r), atazanavir (ATV), favipiravir (FVP), nevirapine (NVP), efavirenz (EFV), oseltamivir, remdesivir, anakinra, tocilizumab (TCZ), eculizumab, heme oxygenase 1 (HO-1) regulators, renin–angiotensin–aldosterone system (RAAS) inhibitors, ivermectin, and nitazoxanide. Drug-gene variant pairs that may alter the therapeutic outcomes in COVID-19 patients are presented. The major drug variant pairs that associated with variations in clinical efficacy include CQ/HCQ ( CYP2C8, CYP2D6, ACE2, and HO-1); azithromycin ( ABCB1); LPV/r ( SLCO1B1, ABCB1, ABCC2 and CYP3A); NVP ( ABCC10); oseltamivir (CES1 and ABCB1); remdesivir ( CYP2C8, CYP2D6, CYP3A4, and OATP1B1); anakinra ( IL-1a); and TCZ ( IL6R and FCGR3A). The major drug variant pairs that associated with variations in adverse effects include CQ/HCQ ( G6PD; hemolysis and ABCA4; retinopathy), ATV ( MDR1 and UGT1A1*28; hyperbilirubinemia; and APOA5; dyslipidemia), NVP ( HLA-DRB1*01, HLA-B*3505 and CYP2B6; skin rash and MDR1; hepatotoxicity), and EFV ( CYP2B6; depression and suicidal tendencies).

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          Most cited references115

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          Hydroxychloroquine and azithromycin as a treatment of COVID-19: results of an open-label non-randomized clinical trial

          Background Chloroquine and hydroxychloroquine have been found to be efficient on SARS-CoV-2, and reported to be efficient in Chinese COV-19 patients. We evaluate the role of hydroxychloroquine on respiratory viral loads. Patients and methods French Confirmed COVID-19 patients were included in a single arm protocol from early March to March 16th, to receive 600mg of hydroxychloroquine daily and their viral load in nasopharyngeal swabs was tested daily in a hospital setting. Depending on their clinical presentation, azithromycin was added to the treatment. Untreated patients from another center and cases refusing the protocol were included as negative controls. Presence and absence of virus at Day6-post inclusion was considered the end point. Results Six patients were asymptomatic, 22 had upper respiratory tract infection symptoms and eight had lower respiratory tract infection symptoms. Twenty cases were treated in this study and showed a significant reduction of the viral carriage at D6-post inclusion compared to controls, and much lower average carrying duration than reported of untreated patients in the literature. Azithromycin added to hydroxychloroquine was significantly more efficient for virus elimination. Conclusion Despite its small sample size our survey shows that hydroxychloroquine treatment is significantly associated with viral load reduction/disappearance in COVID-19 patients and its effect is reinforced by azithromycin.
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            In Vitro Antiviral Activity and Projection of Optimized Dosing Design of Hydroxychloroquine for the Treatment of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)

            Abstract Background The Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) first broke out in Wuhan (China) and subsequently spread worldwide. Chloroquine has been sporadically used in treating SARS-CoV-2 infection. Hydroxychloroquine shares the same mechanism of action as chloroquine, but its more tolerable safety profile makes it the preferred drug to treat malaria and autoimmune conditions. We propose that the immunomodulatory effect of hydroxychloroquine also may be useful in controlling the cytokine storm that occurs late-phase in critically ill SARS-CoV-2 infected patients. Currently, there is no evidence to support the use of hydroxychloroquine in SARS-CoV-2 infection. Methods The pharmacological activity of chloroquine and hydroxychloroquine was tested using SARS-CoV-2 infected Vero cells. Physiologically-based pharmacokinetic models (PBPK) were implemented for both drugs separately by integrating their in vitro data. Using the PBPK models, hydroxychloroquine concentrations in lung fluid were simulated under 5 different dosing regimens to explore the most effective regimen whilst considering the drug’s safety profile. Results Hydroxychloroquine (EC50=0.72 μM) was found to be more potent than chloroquine (EC50=5.47 μM) in vitro. Based on PBPK models results, a loading dose of 400 mg twice daily of hydroxychloroquine sulfate given orally, followed by a maintenance dose of 200 mg given twice daily for 4 days is recommended for SARS-CoV-2 infection, as it reached three times the potency of chloroquine phosphate when given 500 mg twice daily 5 days in advance. Conclusions Hydroxychloroquine was found to be more potent than chloroquine to inhibit SARS-CoV-2 in vitro.
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              Epidemiologic Features and Clinical Course of Patients Infected With SARS-CoV-2 in Singapore

              Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in Wuhan, China, in December 2019 and has spread globally with sustained human-to-human transmission outside China.
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                Author and article information

                Contributors
                osama.badary@bue.edu.eg
                Journal
                Pharmacogenomics J
                Pharmacogenomics J
                The Pharmacogenomics Journal
                Nature Publishing Group UK (London )
                1470-269X
                1473-1150
                4 February 2021
                : 1-10
                Affiliations
                [1 ]GRID grid.440862.c, ISNI 0000 0004 0377 5514, Clinical Pharmacy Practice Department, Faculty of Pharmacy, , The British University in Egypt (BUE), ; Cairo, Egypt
                [2 ]GRID grid.7269.a, ISNI 0000 0004 0621 1570, Clinical Pharmacy Department, Faculty of Pharmacy, , Ain Shams University, ; Cairo, Egypt
                Author information
                http://orcid.org/0000-0002-5676-6692
                Article
                209
                10.1038/s41397-021-00209-9
                7859465
                33542445
                ed2913ae-ae3d-4d58-a23e-8599dfcc9676
                © The Author(s), under exclusive licence to Springer Nature Limited part of Springer Nature 2021

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 13 June 2020
                : 7 December 2020
                : 15 January 2021
                Categories
                Review Article

                Pharmacology & Pharmaceutical medicine
                genetic association study,drug development
                Pharmacology & Pharmaceutical medicine
                genetic association study, drug development

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