Skip to main content
Log in

Estimation of apparent clearance of valproic acid in adult Saudi patients

  • Research Article
  • Published:
International Journal of Clinical Pharmacy Aims and scope Submit manuscript

Abstract

Background Valproic acid is one of several antiepileptic medications requiring therapeutic drug monitoring due to its complex and wide pharmacokinetic interindividual variability. Objective The objective of this study was to determine the population pharmacokinetics of valproic acid in adult Saudi patients and to identify factors that explain its pharmacokinetic variability. Setting Tertiary referral teaching hospital, Riyadh, Saudi Arabia. Method A retrospective chart review was performed at King Saud University Medical City of patients who received oral valproic acid. The population pharmacokinetic models were developed using Monolix 4.4. After development of the base model, we investigated several covariates including age, sex, weight, total daily dose, and cotherapy with carbamazepine and phenytoin. Main outcome measures the pharmacokinetic parameters of valproic acid and the variables that contributing towards its inter-individual variability. Results The analysis included a total of 54 valproic acid plasma concentrations from 54 patients (42.5% male). The data were sufficiently described by a one-compartment model with linear absorption and elimination processes. Average parameter estimates for valproic acid apparent clearance (CL/F) and apparent volume of distribution (V/F) were 0.14 L/h and 37.7 L (fixed), respectively. The inter-individual variability (coefficients of variation) in CL/F was 12%. The most significant covariates for valproic acid CL/F were age, body weight, total daily dose, and cotherapy with carbamazepine and phenytoin. Conclusion This model showed significant inter-individual variability between subjects. Our findings showed that patient age, body weight, total daily dose, and cotherapy with carbamazepine and phenytoin are the most significant covariates of valproic acid clearance. Collectively, healthcare providers should take these factors in consideration for optimal valproic acid dosage regimen.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Perucca E. An introduction to antiepileptic drugs. Epilepsia. 2005;46(Suppl 4):31–7.

    Article  CAS  PubMed  Google Scholar 

  2. Gidal BE, Pitterle ME, Spencer NW, Maly MM. Relationship between valproic acid dosage, plasma concentration and clearance in adult monotherapy patients with epilepsy. J Clin Pharm Ther. 1995;20(4):215–9.

    Article  CAS  PubMed  Google Scholar 

  3. Aluisio AR, Zehtabchi S. Valproate for adult migraine prophylaxis. Am Fam Physician. 2016;94(9):Online.

  4. Shah P, Mato A, Luger SM. Valproic acid for the treatment of myeloid malignancies. Cancer. 2008;112(10):2324–5.

    Article  CAS  PubMed  Google Scholar 

  5. Griswold KS, Pessar LF. Management of bipolar disorder. Am Fam Physician. 2000;62(6):1343–53, 57–8.

  6. Vella T, Mifsud J. Interactions between valproic acid and quetiapine/olanzapine in the treatment of bipolar disorder and the role of therapeutic drug monitoring. J Pharm Pharmacol. 2014;66(6):747–59.

    CAS  PubMed  Google Scholar 

  7. Gugler R, von Unruh GE. Clinical pharmacokinetics of valproic acid. Clin Pharmacokinet. 1980;5(1):67–83.

    Article  CAS  PubMed  Google Scholar 

  8. Zaccara G, Messori A, Moroni F. Clinical pharmacokinetics of valproic acid–1988. Clin Pharmacokinet. 1988;15(6):367–89.

    Article  CAS  PubMed  Google Scholar 

  9. Smith RL, Haslemo T, Refsum H, Molden E. Impact of age, gender and CYP2C9/2C19 genotypes on dose-adjusted steady-state serum concentrations of valproic acid-a large-scale study based on naturalistic therapeutic drug monitoring data. Eur J Clin Pharmacol. 2016;72(9):1099–104.

    Article  CAS  PubMed  Google Scholar 

  10. Correa T, Rodriguez I, Romano S. Population pharmacokinetics of valproate in Mexican children with epilepsy. Biopharm Drug Dispos. 2008;29(9):511–20.

    Article  CAS  PubMed  Google Scholar 

  11. El Desoky ES, Fuseau E, El Din Amry S, Cosson V. Pharmacokinetic modelling of valproic acid from routine clinical data in Egyptian epileptic patients. Eur J Clin Pharmacol. 2004;59(11):783–90.

    Article  CAS  Google Scholar 

  12. Lin WW, Jiao Z, Wang CL, Wang HY, Ma CL, Huang PF, et al. Population pharmacokinetics of valproic acid in adult Chinese epileptic patients and its application in an individualized dosage regimen. Ther Drug Monit. 2015;37(1):76–83.

    Article  CAS  PubMed  Google Scholar 

  13. Yukawa E, To H, Ohdo S, Higuchi S, Aoyama T. Population-based investigation of valproic acid relative clearance using nonlinear mixed effects modeling: influence of drug-drug interaction and patient characteristics. J Clin Pharmacol. 1997;37(12):1160–7.

    Article  CAS  PubMed  Google Scholar 

  14. Serrano BB, Garcia Sanchez MJ, Otero MJ, Buelga DS, Serrano J, Dominguez-Gil A. Valproate population pharmacokinetics in children. J Clin Pharm Ther. 1999;24(1):73–80.

    Article  CAS  PubMed  Google Scholar 

  15. Klotz U, Rapp T, Muller WA. Disposition of valproic acid in patients with liver disease. Eur J Clin Pharmacol. 1978;13(1):55–60.

    Article  CAS  PubMed  Google Scholar 

  16. DeVane CL. Pharmacokinetics, drug interactions, and tolerability of valproate. Psychopharmacol Bull. 2003;37(Suppl 2):25–42.

    PubMed  Google Scholar 

  17. Hamilton RA, Garnett WR, Kline BJ, Pellock JM. Effects of food on valproic acid absorption. Am J Hosp Pharm. 1981;38(10):1490–3.

    CAS  PubMed  Google Scholar 

  18. Lavielle M, Mentre F. Estimation of population pharmacokinetic parameters of saquinavir in HIV patients with the MONOLIX software. J Pharmacokinet Pharmacodyn. 2007;34(2):229–49.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Blanco-Serrano B, Otero MJ, Santos-Buelga D, Garcia-Sanchez MJ, Serrano J, Dominguez-Gil A. Population estimation of valproic acid clearance in adult patients using routine clinical pharmacokinetic data. Biopharm Drug Dispos. 1999;20(5):233–40.

    Article  CAS  PubMed  Google Scholar 

  20. Methaneethorn J. Population pharmacokinetics of valproic acid in patients with Mania: implication for individualized dosing regimens. Clin Ther. 2017;39(6):1171–81.

    Article  CAS  PubMed  Google Scholar 

  21. Jankovic SM, Milovanovic JR. Pharmacokinetic modeling of valproate from clinical data in Serbian epileptic patients. Methods Find Exp Clin Pharmacol. 2007;29(10):673–9.

    Article  CAS  PubMed  Google Scholar 

  22. Jankovic SM, Milovanovic JR, Jankovic S. Factors influencing valproate pharmacokinetics in children and adults. Int J Clin Pharmacol Ther. 2010;48(11):767–75.

    Article  CAS  PubMed  Google Scholar 

  23. Jiang D, Bai X, Zhang Q, Lu W, Wang Y, Li L, et al. Effects of CYP2C19 and CYP2C9 genotypes on pharmacokinetic variability of valproic acid in Chinese epileptic patients: nonlinear mixed-effect modeling. Eur J Clin Pharmacol. 2009;65(12):1187–93.

    Article  CAS  PubMed  Google Scholar 

  24. Nakashima H, Oniki K, Nishimura M, Ogusu N, Shimomasuda M, Ono T, et al. Determination of the optimal concentration of valproic acid in patients with epilepsy: a population pharmacokinetic-pharmacodynamic analysis. PLoS ONE. 2015;10(10):e0141266.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Park HM, Kang SS, Lee YB, Shin DJ, Kim ON, Lee SB, et al. Population pharmacokinetics of intravenous valproic acid in Korean patients. J Clin Pharm Ther. 2002;27(6):419–25.

    Article  CAS  PubMed  Google Scholar 

  26. Vucicevic K, Miljkovic B, Pokrajac M, Prostran M, Martinovic Z, Grabnar I. The influence of drug–drug interaction and patients’ characteristics on valproic acid’s clearance in adults with epilepsy using nonlinear mixed effects modeling. Eur J Pharm Sci. 2009;38(5):512–8.

    Article  CAS  PubMed  Google Scholar 

  27. Methaneethorn J. A systematic review of population pharmacokinetics of valproic acid. Br J Clin Pharmacol. 2018;84(5):816–34.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Birnbaum AK, Ahn JE, Brundage RC, Hardie NA, Conway JM, Leppik IE. Population pharmacokinetics of valproic acid concentrations in elderly nursing home residents. Ther Drug Monit. 2007;29(5):571–5.

    Article  CAS  PubMed  Google Scholar 

  29. Ibarra M, Vazquez M, Fagiolino P, Derendorf H. Sex related differences on valproic acid pharmacokinetics after oral single dose. J Pharmacokinet Pharmacodyn. 2013;40(4):479–86.

    Article  CAS  PubMed  Google Scholar 

  30. Chatzistefanidis D, Georgiou I, Kyritsis AP, Markoula S. Functional impact and prevalence of polymorphisms involved in the hepatic glucuronidation of valproic acid. Pharmacogenomics. 2012;13(9):1055–71.

    Article  CAS  PubMed  Google Scholar 

  31. Ho PC, Abbott FS, Zanger UM, Chang TK. Influence of CYP2C9 genotypes on the formation of a hepatotoxic metabolite of valproic acid in human liver microsomes. Pharmacogenomics J. 2003;3(6):335–42.

    Article  CAS  PubMed  Google Scholar 

  32. Kiang TK, Ho PC, Anari MR, Tong V, Abbott FS, Chang TK. Contribution of CYP2C9, CYP2A6, and CYP2B6 to valproic acid metabolism in hepatic microsomes from individuals with the CYP2C9*1/*1 genotype. Toxicol Sci. 2006;94(2):261–71.

    Article  CAS  PubMed  Google Scholar 

  33. Tan L, Yu JT, Sun YP, Ou JR, Song JH, Yu Y. The influence of cytochrome oxidase CYP2A6, CYP2B6, and CYP2C9 polymorphisms on the plasma concentrations of valproic acid in epileptic patients. Clin Neurol Neurosurg. 2010;112(4):320–3.

    Article  PubMed  Google Scholar 

  34. Zhu MM, Li HL, Shi LH, Chen XP, Luo J, Zhang ZL. The pharmacogenomics of valproic acid. J Hum Genet. 2017;62(12):1009–14.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The authors acknowledge support from the College of Pharmacy Research Center and the Deanship of Scientific Research, King Saud University (Riyadh, Saudi Arabia).

Funding

There was no specific funding source for this study.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Saeed Alqahtani.

Ethics declarations

Conflicts of interests

The author has no conflicts of interest to declare.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Alqahtani, S., Alandas, N. & Alsultan, A. Estimation of apparent clearance of valproic acid in adult Saudi patients. Int J Clin Pharm 41, 1056–1061 (2019). https://doi.org/10.1007/s11096-019-00864-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11096-019-00864-w

Keywords

Navigation