1.Erratum: R-based reproduction of the estimation process hidden behind NONMEM Part 2: First-order conditional estimation
Translational and Clinical Pharmacology 2018;26(2):99-99
The equations on page 162 should be corrected.
2.Erratum: Development of R packages: ‘NonCompart’ and ‘ncar’ for noncompartmental analysis (NCA)
Hyungsub KIM ; Sungpil HAN ; Yong Soon CHO ; Seok Kyu YOON ; Kyun Seop BAE
Translational and Clinical Pharmacology 2018;26(3):141-141
There are some errors in the published article. The authors would like to make corrections in the original version of the article.
3.Analytical solution of linear multi-compartment models with non-zero initial condition and its implementation with R
David Z D'ARGENIO ; Kyun Seop BAE
Translational and Clinical Pharmacology 2019;27(2):43-51
The analytical solution for multi-compartment models with a non-zero initial condition is complex because of the inter-compartmental transfer. An elegant solution and its implementation in the ‘wnl' R package can be useful in solving examples of textbooks and developing software of therapeutic drug monitoring, pharmacokinetic simulation, and parameter estimation. This solution uses Laplace transformation, convolution, matrix inversion, and the fact that the general solution of an inhomogeneous ordinary differential equation is the sum of a homogenous and a particular solution, together.
Drug Monitoring
4.R-based reproduction of the estimation process hidden behind NONMEM® Part 2: First-order conditional estimation.
Translational and Clinical Pharmacology 2016;24(4):161-168
The first-order conditional estimation (FOCE) method is more complex than the first-order (FO) approximation method because it estimates the empirical Bayes estimate (EBE) for each iteration. By contrast, it is a further approximation of the Laplacian (LAPL) method, which uses second-order expansion terms. FOCE without INTERACTION can only be used for an additive error model, while FOCE with INTERACTION (FOCEI) can be used for any error model. The formula for FOCE without INTERACTION can be derived directly from the extension of the FO method, while the FOCE with INTERACTION method is a slight simplification of the LAPL method. Detailed formulas and R scripts are presented here for the reproduction of objective function values by NONMEM.
Bays
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Methods
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Reproduction*
5.Bioequivalence data analysis
Gowooni PARK ; Hyungsub KIM ; Kyun-Seop BAE
Translational and Clinical Pharmacology 2020;28(4):175-180
SAS® is commonly used for bioequivalence (BE) data analysis. R is a free and open software for general purpose data analysis, and is less frequently used than SAS® for BE data analysis. This tutorial explains how R can be used for BE data analysis to generate comparable results with SAS® . The main SAS® procedures for BE data analysis are PROC GLM and PROC MIXED, and the corresponding R main packages are “sasLM” and “nlme” respectively. For fixed effects only or balanced data, the SAS® PROC GLM and R “sasLM” provide good estimates; however, for a mixed-effects model with unbalanced data, the SAS® PROC MIXED and R “nlme” are better for providing estimates without bias. The SAS® and R scripts are provided for convenience.
6.Bioequivalence data analysis
Gowooni PARK ; Hyungsub KIM ; Kyun-Seop BAE
Translational and Clinical Pharmacology 2020;28(4):175-180
SAS® is commonly used for bioequivalence (BE) data analysis. R is a free and open software for general purpose data analysis, and is less frequently used than SAS® for BE data analysis. This tutorial explains how R can be used for BE data analysis to generate comparable results with SAS® . The main SAS® procedures for BE data analysis are PROC GLM and PROC MIXED, and the corresponding R main packages are “sasLM” and “nlme” respectively. For fixed effects only or balanced data, the SAS® PROC GLM and R “sasLM” provide good estimates; however, for a mixed-effects model with unbalanced data, the SAS® PROC MIXED and R “nlme” are better for providing estimates without bias. The SAS® and R scripts are provided for convenience.
7.A simple time-to-event model with NONMEM featuring right-censoring
Quyen Thi TRAN ; Jung-woo CHAE ; Kyun-Seop BAE ; Hwi-yeol YUN
Translational and Clinical Pharmacology 2022;30(2):75-82
In healthcare situations, time-to-event (TTE) data are common outcomes. A parametric approach is often employed to handle TTE data because it is possible to easily visualize different scenarios via simulation. Not all pharmacometricians are familiar with the use of non-linear mixed effects models (NONMEMs) to deal with TTE data. Therefore, this tutorial simply explains how to analyze TTE data using NONMEM. We show how to write the code and evaluate the model. We also provide an example of a hands-on model for training.
8.Implementation of Miettinen-Nurminen score method with or without stratification in R
Translational and Clinical Pharmacology 2022;30(3):155-162
Analysis of a 2 × 2 table for clinical data involves computing the point estimate and confidence interval for risk difference, relative risk, or odds ratio. While point estimates of these comparative parameters are uniquely defined, several statistical methods have been proposed to estimate the confidence interval for each parameter. The Miettinen-Nurminen (MN) score method is expected to be used increasingly over traditional interval estimation methods. The MN score method has not been previously implemented in R software for data with stratification. There is a need for a comprehensive software implementation of the MN score method. This article describes the implementation of the MN score method in the sasLM R software package. To demonstrate the usage of the sasLM functions introduced, recently published clinical data are provided as examples.
9.Pharmacodynamic Comparison of Two Formulations of Voglibose 0.3-mg Tablet.
Mi Jo KIM ; Hyeong Seok LIM ; Sang Heon CHO ; Kyun Seop BAE
Journal of Korean Society for Clinical Pharmacology and Therapeutics 2013;21(1):34-40
BACKGROUND: Voglibose, an inhibitor of alpha-glucosidase of the small intestine brush border, is used to treat type 2 diabetic patients. Bioequivalence test based on pharmacokinetic parameters is difficult because voglibose does not cross the enterocytes after ingestion. This study was conducted to establish bioequivalence of two formulations of 0.3-mg voglibose with pharmacodynamic endpoints. METHODS: This study was an open, single-dose, randomized, 6-sequence, 3-period crossover design in healthy volunteers. In each period, subjects received placebo or three tablets of either test formulation or reference formulation with sucrose, with a 7-day washout period each dosing period. Serial blood samples were collected after each administration. The maximum concentrations of serum glucose and serum insulin (C(max)(G) and C(max)(I)) and the area under the serum concentration - time curve from dosing to 2 or 4 hours after dosing for serum glucose and insulin (AUC(0-2h)(G), AUC(0-4h)(G), AUC(0-2h)(I) and AUC(0-4h)(I), respectively) were determined by noncompartmental analysis. Formulation-related differences were tested in accordance with the Korean regulatory bioequivalence criteria. RESULTS: A total of 54 subjects completed study in accordance with protocol. The geometric mean ratios (GMRs) of the test formulation to the reference formulation for Cmax(G), AUC(0-2h)(G), AUC(0-4h)(G), C(max)(I), AUC(0-2h)(I) and AUC(0-4h)(I) were 0.945, 1.014, 0.995, 0.937, 0.985 and 0.983, respectively and the 90% confidence intervals (CIs) of corresponding values were 0.985-1.026, 0.991-1.038, 0.977-1.014, 0.830-1.057, 0.901-1.078 and 0.911-1.014, respectively. CONCLUSION: This single-dose study found that two formulations of 0.3-mg voglibose did not meet the regulatory criteria for bioequivalence in these healthy volunteers.
alpha-Glucosidases
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Cross-Over Studies
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Eating
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Enterocytes
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Glucose
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Humans
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Inositol
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Insulin
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Intestine, Small
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Microvilli
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Sucrose
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Tablets
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Therapeutic Equivalency
10.Forensic science meets clinical pharmacology: pharmacokinetic model based estimation of alcohol concentration of a defendant as requested by a local prosecutor's office.
Hyeong Seok LIM ; Jea Hyen SOUNG ; Kyun Seop BAE
Translational and Clinical Pharmacology 2017;25(1):5-9
Drunk driving is a serious social problem. We estimated the blood alcohol concentration of a defendant on the request of local prosecutor's office in Korea. Based on the defendant's history, and a previously constructed pharmacokinetic model for alcohol, we estimated the possible alcohol concentration over time during his driving using a Bayesian method implemented in NONMEM®. To ensure generalizability and to take the parameter uncertainty of the alcohol pharmacokinetic models into account, a non-parametric bootstrap with 1,000 replicates was applied to the Bayesian estimations. The current analysis enabled the prediction of the defendant's possible blood alcohol concentrations over time with a 95% prediction interval. The results showed a high probability that the alcohol concentration was ≥ 0.05% during driving. The current estimation of the alcohol concentration during driving by the Bayesian method could be used as scientific evidence during court trials.
Bayes Theorem
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Blood Alcohol Content
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Driving Under the Influence
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Forensic Sciences*
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Korea
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Pharmacology, Clinical*
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Social Problems
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Uncertainty