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Background: The initial dose of tacrolimus after liver transplantation (LT) is critical for rapidly achieving the steady state of the drug concentration, minimizing the potential adverse reactions and warranting long-term patient prognosis. We aimed to develop and validate a genotype-guided model for determining personalized initial dose of tacrolimus.
Methods: By combining pharmacokinetic modeling, pharmacogenomic analysis and multiple statistical methods, we developed a genotype-guided model to predict individualized tacrolimus initial dose after LT in the discovery (n = 150) and validation cohorts (n = 97) respectively. This model was further validated in a prospective, randomized and single-blind clinical trial from August, 2021 to February, 2022 (n = 40, ChiCTR2100050288).
Findings: Our model included donor's and recipient's genotypes, recipient's weight and total bilirubin, which achieved an area under the curve of receiver operating characteristic curve (AUC of ROC) of 0.88 and 0.79 in the discovery and validation cohorts, respectively. We found that patients who were given tacrolimus within the recommended concentration range (RCR) (4-10 ng/mL), the new-onset metabolic syndromes are lower, especially for new-onset diabetes (p = 0.043). In the clinical trial, compared to those in experience-based (EB) group, patients in the model-based (MB) group were more likely to achieving the RCR (75% 40%, p = 0.025) with a more variable individualized dose (0.023-0.096 mg/kg/day 0.045-0.057 mg/kg/day). Moreover, significantly fewer medication adjustments were required for the MB group than the EB group (2.75 ± 2.01 6.05 ± 3.35, p = 0.001).
Interpretation: Our genotype-based model significantly improved the initial dosing accuracy of tacrolimus and reduced the number of medication adjustments, which are critical for improving the prognosis of LT patients.
Funding: National Natural Science Foundation of China, Shanghai three-year action plan, National Science and Technology Major Project of China.
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http://dx.doi.org/10.1016/j.eclinm.2022.101752 | DOI Listing |
Georgian Med News
June 2025
4Department of Cardiac Surgery and Heart Transplantation, Joint-Stock Company "National Scientific Center of Surgery named after A.N. Syzganov", Almaty, Kazakhstan.
Objective: To evaluate the clinical outcome, safety, and application of personalized therapy using pharmacogenetic warfarin dosing algorithms in cardiac surgery patients systemically.
Methods: This systematic review focused on 17 published studies between January 2015 to March 2025 regarding warfarin dosing algorithms incorporating CYP2C9 and VKORC1 polymorphisms in patients who underwent cardiac surgery. The primary outcomes were TTR, BER, and INR stability.
NPJ Genom Med
August 2025
Pharmaceutical Sciences Research Center, Department of Pharmacy, Children's Hospital of Nanjing Medical University, Nanjing, China.
Personalized precision dosing remains an unmet clinical need. This study used population pharmacokinetic (PopPK) modeling to evaluate transitioning lacosamide (LCM) in children with epilepsy from body weight (BW)-based (mg/kg) to simplified BW-band or fixed-dose (mg) regimens. Real-world data from 190 patients were analyzed using nonlinear mixed-effects modeling program, comparing a BW-based model (Model I) and a genotype-guided model (Model II); the latter showed superior predictive performance.
View Article and Find Full Text PDFFront Physiol
July 2025
Food Allergy Institute, Long Beach, CA, United States.
Clinical trials of a treatment in traditional mass medicine are based on the concept of proof of efficacy. It must be proven for a group of subjects that meet certain selection criteria. Subject variability must be demonstrated to exist and yet not to invalidate the proof of efficacy.
View Article and Find Full Text PDFDrug Alcohol Depend
September 2025
Crescenz VA Medical Center, Philadelphia, PA 19104, United States; Department of Psychiatry, University of Pennsylvania, Philadelphia, PA 19104, United States. Electronic address:
Background: Few individuals with alcohol use disorder (AUD) receive treatment. Previous studies have shown drinking behavior, psychological problems, and substance dependence to predict treatment seeking. However, to date, no studies have incorporated polygenic scores (PGS), a measure of genetic risk for AUD.
View Article and Find Full Text PDFJ Am Heart Assoc
July 2025
Division of Cardiology and McAllister Heart Institute, School of Medicine University of North Carolina at Chapel Hill Chapel Hill NC USA.
Background: Use of genotyping to guide antiplatelet therapy is associated with improved clinical outcomes in patients naïve to P2Y inhibitors undergoing percutaneous coronary intervention. The relationship between genotype and clinical outcomes in patients on maintenance clopidogrel at the time of percutaneous coronary intervention is unknown.
Methods: This was a retrospective, multicenter cohort study.