Pharmacopsychiatry 2014; 47(07): 268-269
DOI: 10.1055/s-0034-1390413
Letter
© Georg Thieme Verlag KG Stuttgart · New York

Katayama et al.: Therapeutic Window of Lamotrigine for Mood Disorders: A Naturalistic Retrospective Study. Pharmacopsychiatry 2014; 47: 111–114

H. Grunze
1   Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, United Kingdom
,
J. Walden
2   DRV Westfalen, Wissenschaftspark, Gelsenkirchen, Germany
› Author Affiliations
Further Information

Publication History

Publication Date:
06 October 2014 (online)

Abstract

Katayama and colleagues proposed in their article a therapeutic window for lamotrigine in affective disorders between 5 and 11 μg/mL. Despite potential differences in lamotrigine metabolism, the results of their retrospective study in a Japanese population match nicely with what we have previously reported in a Caucasian population with rapid cycling bipolar disorder. It is suggested that not only in epilepsy, but also in mood-disordered patients clinicians should rather consider lamotrigine plasma levels than dosage when in doubt about the efficacy of treatment.

 
  • References

  • 1 Katayama Y, Terao T, Kamei K et al. Therapeutic window of lamotrigine for mood disorders: a naturalistic retrospective study. Pharmacopsychiatry 2014; 47: 111-114
  • 2 Amann B, Born C, Crespo JM et al. Lamotrigine: when and where does it act in affective disorders? A systematic review. J Psychopharmacol 2011; 25: 1289-1294
  • 3 Hirsch LJ, Weintraub D, Du Y et al. Correlating lamotrigine serum concentrations with tolerability in patients with epilepsy. Neurology 2004; 63: 1022-1026
  • 4 Calabrese J, Bowden CL, Sachs G et al. A Placebo-Controlled 18-Month Trial of Lamotrigine and Lithium Maintenance Treatment in Recently Depressed Patients with Bipolar I Disorder. J Clin Psychiatry 2003; 64: 1024
  • 5 Bowden CL, Calabrese JR, Sachs G et al. A placebo-controlled 18-month trial of lamotrigine and lithium maintenance treatment in recently manic or hypomanic patients with bipolar I disorder. Arch Gen Psychiatry 2003; 60: 392-400
  • 6 US Prescriber Information Lamictal® . https://www.gsksource.com/gskprm/htdocs/documents/LAMICTAL-PI-MG.PDF 2-6-2014. Ref Type: Electronic Citation
  • 7 Reimers A, Helde G, Brodtkorb E. Ethinyl estradiol, not progestogens, reduces lamotrigine serum concentrations. Epilepsia 2005; 46: 1414-1417
  • 8 Clark CT, Klein AM, Perel JM et al. Lamotrigine dosing for pregnant patients with bipolar disorder. Am J Psychiatry 2013; 170: 1240-1247
  • 9 Hussein Z, Posner J. Population pharmacokinetics of lamotrigine monotherapy in patients with epilepsy: retrospective analysis of routine monitoring data. Br J Clin Pharmacol 1997; 43: 457-465
  • 10 Singkham N, Towanabut S, Lertkachatarn S et al. Influence of the UGT2B7-161C>T polymorphism on the population pharmacokinetics of lamotrigine in Thai patients. Eur J Clin Pharmacol 2013; 69: 1285-1291
  • 11 Walden J, Schaerer L, Schloesser S et al. An open longitudinal study of patients with bipolar rapid cycling treated with lithium or lamotrigine for mood stabilization. Bipolar Disord 2000; 2: 336-339