Pharmacogenetics of antiparkinsonian drug treatment: a systematic review

被引:16
作者
Arbouw, Maurits E. L.
van Vugt, Jeroen P. P.
Egberts, Toine C. G.
Guchelaar, Henk-Jan
机构
[1] Leiden Univ, Med Ctr, Dept Clin Pharm & Toxicol, NL-2300 RC Leiden, Netherlands
[2] Univ Utrecht, Div Pharmacoepidemiol & Pharmacotherapy, Utrecht Inst Pharmaceut Sci, Fac Sci, Utrecht, Netherlands
[3] Med Spectrum Twente, Dept Clin Pharm, Enschede, Netherlands
[4] Med Spectrum Twente, Dept Neurol, Enschede, Netherlands
[5] Univ Med Ctr Utrecht, Dept Clin Pharm, Utrecht, Netherlands
关键词
apolipoproteine E; budipine; catechol-O-methyltransferase; cholecystokinin; dopamine; entacapone; hypocretin; levodopa; monoamine-oxidase; opioid; Parkinson's disease; pergolide; P-glycoprotein; pharmacogenetics; pharmacotherapy; pramipexole; receptors; ropinirole; serotonin; tolcapone;
D O I
10.2217/14622416.8.2.159
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pharmacotherapy is the mainstay in the treatment of Parkinson's disease and the armamentarium of drugs available for the therapy of this disease is still expanding. Anti-Parkinson's disease drugs are effective in reducing the physical symptoms, such as hypokinesia, bradykinesia, rigidity and tremor. However, there is a large interindividual variability in response to anti-Parkinson's disease drugs with respect to both drug efficacy and toxicity. It is thought that genetic variability in genes encoding drug-metabolizing enzymes, drug receptors and proteins involved in pathway signaling is an important factor in determining interindividual variability in drug response. Pharmacogenetics aims at identifying genetic markers associated with drug response. Ideally, knowledge of these genetic markers will enable us to predict an individual's drug response in terms of both efficacy and toxicity. The role of pharmacogenetics in the treatment of Parkinson's disease is relatively unexplored. Therefore, we aim to present a systematic review of the published pharmacogenetic studies in Parkinson's disease and to describe polymorphic genes of interest for future research.
引用
收藏
页码:159 / 176
页数:18
相关论文
共 85 条
[71]   Functional COMT variant predicts response to high dose pyridoxine in Parkinson's disease [J].
Tan, EK ;
Cheah, SY ;
Fook-Chong, S ;
Yew, K ;
Chandran, VR ;
Lum, SY ;
Yi, Z .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2005, 137B (01) :1-4
[72]   CLONING, MOLECULAR CHARACTERIZATION, AND CHROMOSOMAL ASSIGNMENT OF A GENE ENCODING A 2ND D1 DOPAMINE RECEPTOR SUBTYPE - DIFFERENTIAL EXPRESSION PATTERN IN RAT-BRAIN COMPARED WITH THE D1A RECEPTOR [J].
TIBERI, M ;
JARVIE, KR ;
SILVIA, C ;
FALARDEAU, P ;
GINGRICH, JA ;
GODINOT, N ;
BERTRAND, L ;
YANGFENG, TL ;
FREMEAU, RT ;
CARON, MG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (17) :7491-7495
[73]   The anti-Parkinson drug budipine is exported actively out of the brain by P-glycoprotein in mice [J].
Uhr, M ;
Ebinger, M ;
Rosenhagen, MC ;
Grauer, MT .
NEUROSCIENCE LETTERS, 2005, 383 (1-2) :73-76
[74]   Distinct functions of the two isoforms of dopamine D2 receptors [J].
Usiello, A ;
Baik, JH ;
Rougé-Pont, F ;
Picetti, R ;
Dierich, A ;
LeMeur, M ;
Piazza, PV ;
Borrelli, E .
NATURE, 2000, 408 (6809) :199-203
[75]  
VANTOL HHM, 1992, NATURE, V358, P149
[76]   Polymorphisms of dopamine receptor and transporter genes and hallucinations in Parkinson's disease [J].
Wang, J ;
Zhao, CY ;
Chen, B ;
Liu, ZL .
NEUROSCIENCE LETTERS, 2004, 355 (03) :193-196
[77]   Cholecystokinin, cholecystokinin-A receptor and cholecystokinin-B receptor gene polymorphisms in Parkinson's disease [J].
Wang, J ;
Si, YM ;
Liu, ZL ;
Yu, L .
PHARMACOGENETICS, 2003, 13 (06) :365-369
[78]   Association study of dopamine D2, D3 receptor gene polymorphisms with motor fluctuations in PD [J].
Wang, J ;
Liu, ZL ;
Chen, B .
NEUROLOGY, 2001, 56 (12) :1757-1759
[79]   Dopamine D5 receptor gene polymorphism and the risk of levodopa-induced motor fluctuations in patients with Parkinson's disease [J].
Wang, J ;
Liu, ZL ;
Chen, B .
NEUROSCIENCE LETTERS, 2001, 308 (01) :21-24
[80]   Association between catechol-O-methyltransferase gene polymorphisms and wearing-off and dyskinesia in Parkinson's disease [J].
Watanabe, M ;
Harada, S ;
Nakamura, T ;
Ohkoshi, N ;
Yoshikawa, K ;
Hayashi, A ;
Shoji, S .
NEUROPSYCHOBIOLOGY, 2003, 48 (04) :190-193