Publications by authors named "J L Terrier"

Background And Objective: Fexofenadine is commonly used as a probe substrate to assess P-glycoprotein (Pgp) activity. While its use in healthy volunteers is well documented, data in older adult and polymorbid patients are lacking. Age- and disease-related physiological changes are expected to affect the pharmacokinetics of fexofenadine.

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Aims: Liver cytochromes (CYPs) play an important role in drug metabolism but display a large interindividual variability resulting both from genetic and environmental factors. Most drug dose adjustment guidelines are based on genetics performed in healthy volunteers. However, hospitalized patients are not only more likely to be the target of new prescriptions and drug treatment modifications than healthy volunteers, but will also be more subject to polypharmacy, drug-drug interactions, or to suffer from disease or inflammation affecting CYP activities.

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Dexamethasone (DEX) is currently the treatment of choice for patients with oxygen-dependent COVID-19. It has been observed, primarily in vitro, that dexamethasone induces the expression of CYP3A and the ABCB1 gene, which encodes P-glycoprotein (P-gp). This has raised concerns about potential interactions between DEX and substrates of CYP3A and P-gp, such as direct oral anticoagulants (DOAC).

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Article Synopsis
  • The study investigates tacrolimus dosing by analyzing its dose-response relationships, particularly focusing on continuous intravenous administration when oral intake is not possible, leading to potential misinterpretation of blood levels.
  • Utilizing physiologically based pharmacokinetic (PBPK) modeling, the research estimated the oral/intravenous dose ratios and Css/Cmin ratios for tacrolimus under various conditions, including the impact of genetic factors and drug interactions.
  • Findings showed a 4.25 PO/IV dose ratio and a Css/Cmin ratio of 1.40 in healthy subjects, with variations noted for liver donors and recipients, indicating important implications for individualized dosing in clinical settings.
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Trans people have diverse life experiences which may include gender-affirming care (GAC). GAC positively impacts the quality of life of trans adults. However, they are often met with barriers to care and are particularly vulnerable within the healthcare system.

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