Pharmacogenomics of Central Nervous System (CNS) Drugs

被引:16
|
作者
Cacabelos, Ramon [1 ]
机构
[1] Camilo Jose Cela Univ, EuroEspes Biomed Res Ctr, Inst CNS Disorders & Genom Med, EuroEspes Chair Biotechnol & Genom, Bergondo 15165, Corunna, Spain
关键词
CNS disorders; Alzheimer's disease; pharmacogenomics; CYP2D6; CYP2C9; CYP2C19; CYP3A4/5; APOE; transporters; psychotropic drugs; RNA INTERFERENCE; THERAPEUTIC PROSPECTS; GENETIC POLYMORPHISMS; EXPRESSION; TRANSPORTERS; GENOMICS; PROTEIN; IMPACT; FUTURE; ABCB1;
D O I
10.1002/ddr.21039
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Central nervous system (CNS) disorders represent a major problem of health in developed countries, with important consequences in disability and health economics. Recent findings in CNS genomics and pharmacogenomics suggest that the introduction of pharmacogenomic procedures in clinical practice may help to optimize therapeutics (efficacy and safety issues). The genes involved in the pharmacogenomics of CNS drugs fall into five categories: (i) genes associated with CNS pathogenesis; (ii) genes associated with the mechanism of action of drugs; (iii) genes associated with drug metabolism; (iv) genes associated with drug transporters; and (v) pleiotropic genes involved in multifaceted cascades and metabolic reactions. Pharmacogenomics accounts for 30-90% variability in pharmacokinetics and pharmacodynamics. Only 20-30% of the Caucasian population processes normally approximately 60% of the current drugs that are metabolized via CYP2D6, CYP2C9, and CYP2C19. Clinical pharmacogenomics may contribute to personalizing pharmacological treatment, predicting patient/drug-dose selection, minimizing drug interactions, increasing drug efficacy, and reducing unnecessary costs. Drug Dev Res 73 : 461476, 2012. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:461 / 476
页数:16
相关论文
共 50 条
  • [2] Central Nervous System (CNS) Thrombosis
    Th Mantziou
    H Platokouki
    B Karabelas
    Z Kapsimali
    E Adamtziki
    A Covanis
    A Skardoutsou
    A Constantopoulos
    S Aronis
    [J]. Pediatric Research, 1999, 45 : 766 - 766
  • [3] Prediction of the effect of injection volume on the exposure to intrathecal (IT) drugs in the central nervous system (CNS)
    Monine, Michael
    Sullivan, Jenna M.
    Verma, Ajay
    Nestorov, Ivan
    [J]. JOURNAL OF PHARMACOKINETICS AND PHARMACODYNAMICS, 2017, 44 : S80 - S80
  • [4] Central nervous system (CNS) thrombosis.
    Mantziou, T
    Platokouki, H
    Karabelas, B
    Kapsimali, Z
    Adamtziki, E
    Covanis, A
    Skardoutsou, A
    Constantopoulos, A
    Aronis, S
    [J]. PEDIATRIC RESEARCH, 1999, 45 (05) : 766 - 766
  • [5] MRI of central nervous system (CNS) vasculitis
    Abe, Kazuo
    [J]. CURRENT MEDICAL IMAGING REVIEWS, 2006, 2 (04) : 425 - 434
  • [6] "Terpenoids with activity in the Central Nervous System (CNS)".
    Passos, Carolina S.
    Arbo, Marcelo D.
    Rates, Stela. M. K.
    von Poser, Gilsane L.
    [J]. REVISTA BRASILEIRA DE FARMACOGNOSIA-BRAZILIAN JOURNAL OF PHARMACOGNOSY, 2009, 19 (1A): : 140 - 149
  • [7] Bevacizumab and central nervous system (CNS) hemorrhage
    Nathalie Letarte
    Linda R. Bressler
    John L. Villano
    [J]. Cancer Chemotherapy and Pharmacology, 2013, 71 : 1561 - 1565
  • [8] PRIMARY CENTRAL NERVOUS SYSTEM (CNS) PHLEBITIS
    Keat, Karuna
    Levy, Stanley
    [J]. RHEUMATOLOGY, 2019, 58 : 40 - 40
  • [9] PATTERNS OF CENTRAL NERVOUS SYSTEM (CNS) MALFORMATIONS
    Ng, L.
    White, M.
    Murphy, J. F. A.
    [J]. IRISH JOURNAL OF MEDICAL SCIENCE, 2010, 179 : S221 - S222
  • [10] Bevacizumab and central nervous system (CNS) hemorrhage
    Letarte, Nathalie
    Bressler, Linda R.
    Villano, John L.
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2013, 71 (06) : 1561 - 1565