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  1. Article ; Online: Molnupiravir Revisited-Critical Assessment of Studies in Animal Models of COVID-19.

    Rasmussen, Henrik Berg / Hansen, Peter Riis

    Viruses

    2023  Volume 15, Issue 11

    Abstract: Molnupiravir, a prodrug known for its broad antiviral activity, has demonstrated efficacy in animal models of COVID-19, prompting clinical trials, in which initial results indicated a significant effect against the disease. However, subsequent clinical ... ...

    Abstract Molnupiravir, a prodrug known for its broad antiviral activity, has demonstrated efficacy in animal models of COVID-19, prompting clinical trials, in which initial results indicated a significant effect against the disease. However, subsequent clinical studies did not confirm these findings, leading to the refusal of molnupiravir for permanent market authorization in many countries. This report critically assessed 22 studies published in 18 reports that investigated the efficacy of molnupiravir in animal models of COVID-19, with the purpose of determining how well the design of these models informed human studies. We found that the administered doses of molnupiravir in most studies involving animal COVID-19 models were disproportionately higher than the dose recommended for human use. Specifically, when adjusted for body surface area, over half of the doses of molnupiravir used in the animal studies exceeded twice the human dose. Direct comparison of reported drug exposure across species after oral administration of molnupiravir indicated that the antiviral efficacy of the dose recommended for human use was underestimated in some animal models and overestimated in others. Frequently, molnupiravir was given prophylactically or shortly after SARS-CoV-2 inoculation in these models, in contrast to clinical trials where such timing is not consistently achieved. Furthermore, the recommended five-day treatment duration for humans was exceeded in several animal studies. Collectively, we suggest that design elements in the animal studies under examination contributed to a preference favoring molnupiravir, and thus inflated expectations for its efficacy against COVID-19. Addressing these elements may offer strategies to enhance the clinical efficacy of molnupiravir for the treatment of COVID-19. Such strategies include dose increment, early treatment initiation, administration by inhalation, and use of the drug in antiviral combination therapy.
    MeSH term(s) Animals ; Humans ; COVID-19 ; SARS-CoV-2 ; Models, Animal ; Antiviral Agents/therapeutic use
    Chemical Substances molnupiravir (YA84KI1VEW) ; Antiviral Agents
    Language English
    Publishing date 2023-10-25
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2516098-9
    ISSN 1999-4915 ; 1999-4915
    ISSN (online) 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v15112151
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Nucleoside analog GS-441524: pharmacokinetics in different species, safety, and potential effectiveness against Covid-19.

    Rasmussen, Henrik Berg / Thomsen, Ragnar / Hansen, Peter Riis

    Pharmacology research & perspectives

    2022  Volume 10, Issue 2, Page(s) e00945

    Abstract: GS-441524, the parent nucleoside of remdesivir, has been proposed to be effective against Covid-19 based on in vitro studies and studies in animals. However, randomized clinical trials of the agent to treat Covid-19 have not been conducted. Here, we ... ...

    Abstract GS-441524, the parent nucleoside of remdesivir, has been proposed to be effective against Covid-19 based on in vitro studies and studies in animals. However, randomized clinical trials of the agent to treat Covid-19 have not been conducted. Here, we evaluated GS-441524 for Covid-19 treatment based on studies reporting pharmacokinetic parameters of the agent in mice, rats, cats, dogs, monkeys, and the single individual in the first-in-human trial supplemented with information about its activity against severe acute respiratory syndrome coronavirus 2 and safety. A dosing interval of 8 h was considered clinically relevant and used to calculate steady-state plasma concentrations of GS-441524. These ranged from 0.27 to 234.41 μM, reflecting differences in species, doses, and administration routes. Fifty percent maximal inhibitory concentrations of GS-441524 against severe acute respiratory syndrome coronavirus 2 ranged from 0.08 μM to above 10 μM with a median of 0.87 μM whereas concentrations required to produce 90% of the maximal inhibition of the virus varied from 0.18 µM to more than 20 µM with a median of 1.42 µM in the collected data. Most of these concentrations were substantially lower than the calculated steady-state plasma concentrations of the agent. Plasma exposures to orally administered GS-441524, calculated after normalization of doses, were larger for dogs, mice, and rats than cynomolgus monkeys and humans, probably reflecting interspecies differences in oral uptake with reported oral bioavailabilities below 8.0% in cynomolgus monkeys and values as high as 92% in dogs. Reported oral bioavailabilities in rodents ranged from 12% to 57%. Using different presumptions, we estimated human oral bioavailability of GS-441524 at 13% and 20%. Importantly, doses of GS-441524 lower than the 13 mg/kg dose used in the first-in-human trial may be effective against Covid-19. Also, GS-441524 appears to be well-tolerated. In conclusion, GS-441524 has potential for oral treatment of Covid-19.
    MeSH term(s) Adenosine/analogs & derivatives ; Animals ; Antiviral Agents ; COVID-19/drug therapy ; Dogs ; Furans ; Humans ; Mice ; Nucleosides ; Rats ; SARS-CoV-2 ; Triazines
    Chemical Substances Antiviral Agents ; Furans ; Nucleosides ; Triazines ; GS-441524 (1BQK176DT6) ; Adenosine (K72T3FS567)
    Language English
    Publishing date 2022-04-08
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2740389-0
    ISSN 2052-1707 ; 2052-1707
    ISSN (online) 2052-1707
    ISSN 2052-1707
    DOI 10.1002/prp2.945
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Pharmacogenetic testing of CYP2D6, CYP2C19 and CYP2C9 in Denmark: Agreement between publicly funded genotyping tests and the subsequent phenotype classification.

    Baltzer Houlind, Morten / Hansen, Luise / Iversen, Esben / Rasmussen, Henrik Berg / Larsen, Jens Borggaard / Jørgensen, Steffen / Dalhoff, Kim / Damkier, Per / Walls, Anne B / Vermehren, Charlotte / Andersen, Trine Rune Høgh / Kallemose, Thomas / Christrup, Lona / Westergaard, Niels

    Basic & clinical pharmacology & toxicology

    2024  Volume 134, Issue 5, Page(s) 756–763

    MeSH term(s) Cytochrome P-450 CYP2D6/genetics ; Cytochrome P-450 CYP2C9/genetics ; Genotype ; Cytochrome P-450 CYP2C19/genetics ; Pharmacogenomic Testing ; Phenotype ; Denmark
    Chemical Substances Cytochrome P-450 CYP2D6 (EC 1.14.14.1) ; Cytochrome P-450 CYP2C9 (EC 1.14.13.-) ; Cytochrome P-450 CYP2C19 (EC 1.14.14.1)
    Language English
    Publishing date 2024-02-25
    Publishing country England
    Document type Journal Article
    ZDB-ID 2134679-3
    ISSN 1742-7843 ; 1742-7835
    ISSN (online) 1742-7843
    ISSN 1742-7835
    DOI 10.1111/bcpt.13990
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Carboxylesterase 1 genes: systematic review and evaluation of existing genotyping procedures.

    Rasmussen, Henrik Berg / Madsen, Majbritt Busk

    Drug metabolism and personalized therapy

    2018  Volume 33, Issue 1, Page(s) 3–14

    Abstract: The carboxylesterase 1 gene (CES1) encodes a hydrolase that metabolizes commonly used drugs. The CES1-related pseudogene, carboxylesterase 1 pseudogene 1 (CES1P1), has been implicated in gene exchange with CES1 and in the formation of hybrid genes ... ...

    Abstract The carboxylesterase 1 gene (CES1) encodes a hydrolase that metabolizes commonly used drugs. The CES1-related pseudogene, carboxylesterase 1 pseudogene 1 (CES1P1), has been implicated in gene exchange with CES1 and in the formation of hybrid genes including the carboxylesterase 1A2 gene (CES1A2). Hence, the CES1 region is complex. Using in silico PCR and alignment, we assessed the specificity of PCR-assisted procedures for genotyping CES1, CES1A2 and CES1P1 in studies identified in PubMed. We identified 33 such studies and excluded those that were not the first to use a procedure or lacked sequence information. After this 17 studies remained. Ten of these used haplotype-specific amplification, restriction enzyme treatment or amplicon sequencing, and included five that were predicted to lack specificity. All procedures for genotyping of single nucleotide polymorphisms in eight studies lacked specificity. One of these studies also used amplicon sequencing, thus being present in the group above. Some primers and their intended targets were mismatched. We provide experimental evidence that one of the procedures lacked specificity. Additionally, a complex pattern of segmental duplications in the CES1 region was revealed. In conclusion, many procedures for CES1, CES1A2 and CES1P1 genotyping appear to lack specificity. Knowledge about the segmental duplications may improve the typing of these genes.
    MeSH term(s) Carboxylic Ester Hydrolases/genetics ; Genotyping Techniques/methods ; Humans ; Polymorphism, Single Nucleotide/genetics ; Sensitivity and Specificity
    Chemical Substances CES1P1 protein, human (EC 3.1.1.-) ; Carboxylic Ester Hydrolases (EC 3.1.1.-) ; CES1 protein, human (EC 3.1.1.1)
    Language English
    Publishing date 2018-02-11
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review ; Systematic Review
    ZDB-ID 2822040-7
    ISSN 2363-8915 ; 2363-8907
    ISSN (online) 2363-8915
    ISSN 2363-8907
    DOI 10.1515/dmpt-2017-0023
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Novel approach for CES1 genotyping: integrating single nucleotide variants and structural variation.

    Bjerre, Ditte / Berg Rasmussen, Henrik / Indices Consortium, The

    Pharmacogenomics

    2018  Volume 19, Issue 4, Page(s) 349–359

    Abstract: Aim: Development of a specific procedure for genotyping of CES1A1 (CES1) and CES1A2, a hybrid of CES1A1  and the pseudogene CES1P1.: Materials & methods: The number of CES1A1 and CES1A2  copies and that of CES1P1  were determined using real-time PCR. ...

    Abstract Aim: Development of a specific procedure for genotyping of CES1A1 (CES1) and CES1A2, a hybrid of CES1A1  and the pseudogene CES1P1.
    Materials & methods: The number of CES1A1 and CES1A2  copies and that of CES1P1  were determined using real-time PCR. Long range PCRs followed by secondary PCRs allowed sequencing of single nucleotide variants in CES1A1 and CES1A2.
    Results & conclusion: A procedure consisting of two main steps was developed. Its first main step, the copy number determination, informed about presence of CES1A2 . This information enabled choice of PCR in the second main step, which selectively amplified CES1A1 and, if present, also CES1A2, for subsequent sequencing. Examination of 501 DNA samples suggested that our procedure is specific with potential for personalization of drug treatments.
    MeSH term(s) Carboxylic Ester Hydrolases/genetics ; DNA/genetics ; Genotype ; Genotyping Techniques/methods ; Humans ; Polymerase Chain Reaction/methods ; Polymorphism, Single Nucleotide/genetics
    Chemical Substances DNA (9007-49-2) ; Carboxylic Ester Hydrolases (EC 3.1.1.-) ; CES1 protein, human (EC 3.1.1.1)
    Language English
    Publishing date 2018-02-19
    Publishing country England
    Document type Journal Article
    ZDB-ID 2019513-8
    ISSN 1744-8042 ; 1462-2416
    ISSN (online) 1744-8042
    ISSN 1462-2416
    DOI 10.2217/pgs-2016-0145
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Pulmonary administration of remdesivir in the treatment of COVID-19.

    Rasmussen, Henrik Berg / Hansen, Peter Riis / Taboureau, Olivier / Thomsen, Ragnar / Jürgens, Gesche

    The AAPS journal

    2020  Volume 22, Issue 6, Page(s) 121

    MeSH term(s) Adenosine Monophosphate/analogs & derivatives ; Alanine/analogs & derivatives ; Betacoronavirus ; COVID-19 ; Coronavirus Infections/drug therapy ; Humans ; Pandemics ; Pneumonia, Viral ; SARS-CoV-2
    Chemical Substances remdesivir (3QKI37EEHE) ; Adenosine Monophosphate (415SHH325A) ; Alanine (OF5P57N2ZX)
    Keywords covid19
    Language English
    Publishing date 2020-09-17
    Publishing country United States
    Document type Letter ; Comment
    ISSN 1550-7416
    ISSN (online) 1550-7416
    DOI 10.1208/s12248-020-00506-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Disruptive mutations in the serotonin transporter associate serotonin dysfunction with treatment-resistant affective disorder.

    Støier, Jonatan Fullerton / Jørgensen, Trine Nygaard / Sparsø, Thomas / Rasmussen, Henrik Berg / Kumar, Vivek / Newman, Amy Hauck / Blakely, Randy D / Werge, Thomas / Gether, Ulrik / Herborg, Freja

    medRxiv : the preprint server for health sciences

    2023  

    Abstract: Affective or mood disorders are a leading cause of disability worldwide. The serotonergic system has been heavily implicated in the complex etiology and serves as a therapeutic target. The serotonin transporter (SERT) is a major regulator of serotonin ... ...

    Abstract Affective or mood disorders are a leading cause of disability worldwide. The serotonergic system has been heavily implicated in the complex etiology and serves as a therapeutic target. The serotonin transporter (SERT) is a major regulator of serotonin neurotransmission, yet the disease-relevance of impaired SERT function remains unknown. Here, we present the first identification and functional characterization of disruptive coding SERT variants found in patients with psychiatric diseases. In a unique cohort of 144 patients characterized by treatment-resistant chronic affective disorders with a lifetime history of electroconvulsive therapy, we identified two previously uncharacterized coding SERT variants: SERT-N217S and SERT-A500T. Both variants were significantly enriched in the patient cohort compared to GnomAD (SERT-N217S: OR = 151,
    Language English
    Publishing date 2023-08-29
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.08.29.23294386
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Pulmonary administration of remdesivir in the treatment of COVID-19

    Rasmussen, Henrik Berg / Hansen, Peter Riis / Taboureau, Olivier / Thomsen, Ragnar / Jürgens, Gesche

    The AAPS Journal

    2020  Volume 22, Issue 6

    Keywords covid19
    Language English
    Publisher Springer Science and Business Media LLC
    Publishing country us
    Document type Article ; Online
    ISSN 1550-7416
    DOI 10.1208/s12248-020-00506-4
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Blood Pressure and Oxygen Targets on Kidney Injury After Cardiac Arrest.

    Rasmussen, Sebastian Buhl / Jeppesen, Karoline Korsholm / Kjaergaard, Jesper / Hassager, Christian / Schmidt, Henrik / Mølstrøm, Simon / Beske, Rasmus Paulin / Grand, Johannes / Ravn, Hanne Berg / Winther-Jensen, Matilde / Meyer, Martin Abild Stengaard / Møller, Jacob Eifer

    Circulation

    2023  Volume 148, Issue 23, Page(s) 1860–1869

    Abstract: Background: Acute kidney injury (AKI) represents a common and serious complication to out-of-hospital cardiac arrest. The importance of post-resuscitation care targets for blood pressure and oxygenation for the development of AKI is unknown.: Methods!# ...

    Abstract Background: Acute kidney injury (AKI) represents a common and serious complication to out-of-hospital cardiac arrest. The importance of post-resuscitation care targets for blood pressure and oxygenation for the development of AKI is unknown.
    Methods: This is a substudy of a randomized 2-by-2 factorial trial, in which 789 comatose adult patients who had out-of-hospital cardiac arrest with presumed cardiac cause and sustained return of spontaneous circulation were randomly assigned to a target mean arterial blood pressure of either 63 or 77 mm Hg. Patients were simultaneously randomly assigned to either a restrictive oxygen target of a partial pressure of arterial oxygen (Pao
    Results: The main population characteristics at admission were: age, 64 (54-73) years; 80% male; 90% shockable rhythm; and time to return of spontaneous circulation, 18 (12-26) minutes. Patients allocated to a low blood pressure and liberal oxygen target had an increased risk of developing AKI compared with patients with high blood pressure and liberal oxygen target (84/193 [44%] versus 56/187 [30%]; adjusted odds ratio, 1.87 [95% CI, 1.21-2.89]). Multinomial logistic regression revealed that the increased risk of AKI was only related to mild-stage AKI (KDIGO stage 1). There was no difference in risk of AKI in the other groups. Plasma creatinine remained high during hospitalization in the low blood pressure and liberal oxygen target group but did not differ between groups at 6- and 12-month follow-up.
    Conclusions: In comatose patients who had been resuscitated after out-of-hospital cardiac arrest, patients allocated to a combination of a low mean arterial blood pressure and a liberal oxygen target had a significantly increased risk of mild-stage AKI. No difference was found in terms of more severe AKI stages or other kidney-related adverse outcomes, and creatinine had normalized at 1 year after discharge.
    Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03141099.
    MeSH term(s) Adult ; Humans ; Male ; Middle Aged ; Female ; Blood Pressure ; Out-of-Hospital Cardiac Arrest/therapy ; Out-of-Hospital Cardiac Arrest/complications ; Oxygen ; Coma ; Creatinine ; Hypertension/complications ; Acute Kidney Injury/etiology ; Acute Kidney Injury/therapy ; Kidney ; Hypotension/complications
    Chemical Substances Oxygen (S88TT14065) ; Creatinine (AYI8EX34EU)
    Language English
    Publishing date 2023-10-04
    Publishing country United States
    Document type Randomized Controlled Trial ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80099-5
    ISSN 1524-4539 ; 0009-7322 ; 0069-4193 ; 0065-8499
    ISSN (online) 1524-4539
    ISSN 0009-7322 ; 0069-4193 ; 0065-8499
    DOI 10.1161/CIRCULATIONAHA.123.066012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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