Evidence map›Paper›PMID 36001534›Full record

ArticlePloS one2022

Comparative pharmacokinetics of valproic acid among Pakistani and South Korean patients: A population pharmacokinetic study.

Muhammad Usman, Qurrat-Ul-Ain Shaukat, Muhammad Imran Khokhar, Rabiea Bilal, Rizwan Rasul Khan, Hafiz Asad Saeed, Mohsin Ali, Humaira Majeed Khan

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Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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  3. Evaluation ofPharmacogenomics and personalized medicine · 2024
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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Muhammad UsmanInstitute of Pharmaceutical Sciences, University of Veterinary and Animal Sciences, Lahore, Pakistan.
Qurrat-Ul-Ain ShaukatInstitute of Pharmacy, Faculty of Pharmaceutical and Allied Health Sciences, Lahore College for Women University, Lahore, Pakistan.
Muhammad Imran KhokharAmeer-ud-Din Medical College, Post-Graduate Medical Institute (PGMI), Lahore General Hospital, Lahore, Pakistan.
Rabiea BilalCMH Lahore Medical College & IOD, NUMS, Lahore, Pakistan.
Rizwan Rasul KhanDepartment of Medicine, Aziz Fatima Medical & Dental College, Faisalabad, Pakistan.
Hafiz Asad SaeedPak Emirates Military Hospital, Rawalpindi, Pakistan.
Mohsin AliDepartment of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Govt College University, Faisalabad, Pakistan.
Humaira Majeed KhanInstitute of Pharmacy, Faculty of Pharmaceutical and Allied Health Sciences, Lahore College for Women University, Lahore, Pakistan.ORCID 0000-0001-8139-9890

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe pharmacokinetics of valproic acid have been evaluated in a variety of populations however, the comparison in two different populations was yet to be reported. This study is aimed to compare the pharmacokinetics of valproic acid in Pakistani and South Korean patients.

methodThe therapeutic drug monitoring (TDM) data of valproic acid from 92 Pakistani patients with 218 samples was combined with the data of 99 South Korean patients with 335 samples in order to form a pooled dataset of 191 patients with 553 samples. Population pharmacokinetic model was developed on NONMEM® software by using first order conditional estimation method for estimation of pharmacokinetic parameters. The influence of different covariates including ethnicity was evaluated the stepwise covariate modelling. The final model was evaluated for predictive performance and robustness by using goodness of fit plots and bootstrap analysis respectively.

resultsThe data was better described by one compartment model with first order elimination. The value for clearance (CL) of valproic in pooled data was 0.931 L/h with 43.4% interindividual variability (IIV) while volume of distribution (Vd) was 16.6 L with 22.3% IIV. In covariate analysis, ethnicity and body weight were significant covariates for CL while body weight was also significant for Vd.

conclusionA significant difference in CL of valproic acid among Pakistani and South Korean patients was observed. The model can be used for the dose tailoring of valproic acid based on ethnicity and body weight of Pakistani and South Korean patients.

Indexed as

Models, BiologicalValproic AcidBody WeightHumansPakistanRepublic of KoreaValproic Acid

Identifiers

PMID36001534
PMCPMC9401156

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.