Update on pharmacogenetics in epilepsy: a brief review

被引:57
作者
Szoeke, CEI [1 ]
Newton, M
Wood, JM
Goldstein, D
Berkovic, SF
OBrien, TJ
Sheffield, LJ
机构
[1] Univ Melbourne, Dept Med, Melbourne, Vic, Australia
[2] Royal Melbourne Hosp, Dept Neurol, Melbourne, Vic, Australia
[3] Austin Hlth, Dept Neurol, Melbourne, Vic, Australia
[4] Mental Hlth Res Inst, Dept Pharmacogenom, Melbourne, Vic, Australia
[5] UCL, London, England
[6] Royal Childrens Hosp, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
关键词
D O I
10.1016/S1474-4422(06)70352-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Recent developments in the pharmacogenetics of antiepileptic drugs provide new prospects for predicting the efficacy of treatment and potential side-effects. Epilepsy is a common, serious, and treatable neurological disorder, yet current treatment is limited by high rates of adverse drug reactions and lack of complete seizure control in a significant proportion of patients. The disorder is especially suitable for pharmacogenetic investigation because treatment response can be quantified and side-effects can be assessed with validated measures. Additionally, there is substantial knowledge of the pharmacodynamics and kinetics of antiepileptic drugs, and some candidate genes implicated in the disorder have been identified. However, recent studies of the association of particular genes and their genetic variants with seizure control and adverse drug reactions have not provided unifying conclusions. This article reviews the published work and summarises the state of research in this area. Future directions for research and the application of this technology to the clinical practice of individualising treatment for epilepsy are discussed.
引用
收藏
页码:189 / 196
页数:8
相关论文
共 101 条
  • [1] The Neurotoxicity Scale .2. Results of a patient-based scale assessing neurotoxicity in patients with epilepsy
    Aldenkamp, AP
    Baker, GA
    [J]. EPILEPSY RESEARCH, 1997, 27 (03) : 165 - 173
  • [2] Pharmacogenetics and enzyme induction/inhibition properties of antiepileptic drugs
    Anderson, GD
    [J]. NEUROLOGY, 2004, 63 (10) : S3 - S8
  • [3] Cytochromes P450 and metabolism of xenobiotics
    Anzenbacher, P
    Anzenbacherová, E
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2001, 58 (5-6) : 737 - 747
  • [4] Expression and cellular distribution of multidrug resistance-related proteins in the hippocampus of patients with mesial temporal lobe epilepsy
    Aronica, E
    Gorter, JA
    Ramkema, M
    Redeker, S
    Özbas-Gerçeker, F
    van Vliet, EA
    Scheffer, GL
    Scheper, RJ
    van der Valk, P
    Baayen, JC
    Troost, D
    [J]. EPILEPSIA, 2004, 45 (05) : 441 - 451
  • [5] Overexpression of the human major vault protein in gangliogliomas
    Aronica, E
    Gorter, JA
    van Vliet, EA
    Spliet, WGM
    van Veelen, CWM
    van Rijen, PC
    Leenstra, S
    Ramkema, MD
    Scheffer, GL
    Scheper, RJ
    Sisodiya, SM
    Troost, D
    [J]. EPILEPSIA, 2003, 44 (09) : 1166 - 1175
  • [6] Aynacioglu AS, 1999, BRIT J CLIN PHARMACO, V48, P409
  • [7] Quality of life of people with epilepsy: A European study
    Baker, GA
    Jacoby, A
    Buck, D
    Stalgis, C
    Monnet, D
    [J]. EPILEPSIA, 1997, 38 (03) : 353 - 362
  • [8] BAKER GA, 1994, EPILEPSIA, V35, P80
  • [9] Pharmacogenomics and the evolution of healthcare - Is it time for cost-effectiveness analysis at the individual level?
    Bala, MV
    Zarkin, GA
    [J]. PHARMACOECONOMICS, 2004, 22 (08) : 495 - 498
  • [10] Estimating the cost of epilepsy
    Begley, CE
    Annegers, JF
    Lairson, DR
    Reynolds, TF
    [J]. EPILEPSIA, 1999, 40 : 8 - 13