Dopamine receptors genes polymorphisms in Parkinson patients with levodopa-induced dyskinesia
Autor: | Irina Zhukova, Olga Yu Fedorenko, Yu. S. Mironova, Diana Z Osmanova, Ivan V Pozhidaev, Maxim B. Freidin, Valentina M. Alifirova, Berend Wilffert, Antonius Loonen, Svetlana A. Ivanova |
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Přispěvatelé: | Methods in Medicines evaluation & Outcomes research (M2O), Reproductive Origins of Adult Health and Disease (ROAHD), PharmacoTherapy, -Epidemiology and -Economics, Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET) |
Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
Oncology
endogenous compound genotype adverse event Pharmacology Gene mutation DISEASE single nucleotide polymorphism gender oxidative stress Pharmacology (medical) gene mutation DNA extraction Abnormal Involuntary Movement Scale statistical significance phosphodiesterase I adult levodopa-induced dyskinesia biological marker cohort analysis drug therapy Parkinson disease Psychiatry and Mental health female Neurology Medical genetics genetic marker medicine.symptom Hyperkinesia medicine.drug onset age Levodopa medicine.medical_specialty phenotype gene frequency analyzer male Internal medicine medicine Genetic predisposition dopamine 4 receptor human levodopa Biological Psychiatry data analysis software Levodopa-induced dyskinesia business.industry dopamine 2 receptor treatment response visually impaired person major clinical study drug metabolism dopamine 3 receptor Dyskinesia DRD2 Neurology (clinical) Gene polymorphism business genetic susceptibility |
Zdroj: | 30th ECNP Congress-Paris 2017 ResearcherID University of Groningen European Neuropsychopharmacology, 27, S590-S590. ELSEVIER SCIENCE BV European Neuropsychopharmacology, 27(Supplement 4). ELSEVIER SCIENCE BV |
ISSN: | 0924-977X |
Popis: | Dopamine receptors genes polymorphisms in Parkinson patients with levodopa-induced dyskinesia I. Pozhidaev(1), V.M. Alifirova(2), M.B. Freidin(3), I.A. Zhukova(2), O.Y. Fedorenko(1), D.Z. Osmanova(1), Y.S. Mironova(2), B. Wilffert(4), S.A. Ivanova(1), A.J.M. Loonen(5) (1)Mental Health Research Institute, Molecular Genetics and Biochemistry, Tomsk, Russia (2)Siberian State Medical University, Neurology and Neurosurgery, Tomsk, Russia (3)Research Institute for Medical Genetics, Laboratory of Population Genetics, Tomsk, Russia (4)Groningen Research Institute of Pharmacy, Pharmacotherapy and Clinical Pharmacology, Groningen, The Netherlands (5)Groningen Research Institute of Pharmacy, Pharmacotherapy in Psychiatric Patients, Groningen, The Netherlands Introduction: Long-term levodopa treatment of Parkinson's disease (PD) is frequently complicated by spontaneously occurring involuntary muscle movements called levodopa-induced dyskinesia (LID). LID are a substantial barrier to effective symptomatic management of Parkinson's disease (PD), as up to 45% of L-DOPA users develop LID within 5 years [1]. The exact pathological mechanism of this complication has not yet been elucidated. A lot of studies nowadays which approved complex genetic nature of LID. And these genes are involved not only for oxidative stress, but in drug metabolism too [2–4]. Objective: This study aimed to investigate a possible contribution of polymorphic variants of DRD1, DRD2, DRD2/ANKK1, DRD3, DRD4 genes in the development of LID in PD patients. Methods: 212 patients with Parkinson's disease on levodopa therapy were investigated. Dyskinesia was measured by using Abnormal Involuntary Movement Scale (AIMS). DNA extraction and fluorogenic 5′-exonuclease TaqMan genotyping assays were conducted according to standard protocols and blind to clinical status of the subjects. Genotyping was carried out on 28 SNPs of dopamine receptors (rs4532, rs936461, rs6275, rs1801028, rs4245147, rs134655, rs6277, rs1076560, rs2283265, rs179997, rs6279, rs1076562, rs2734842, rs2734849, rs11721264, rs167770, rs3773678, rs963468, rs7633291, rs2134655, rs9817063, rs324035, rs1800828, rs167771, rs6280, rs1587756, rs3758653, rs11246226) on the MassARRAY® Analyzer 4 (Agena Bioscience™) using the set SEQUENOM Consumables iPLEX Gold 384. SPSS software was used for statistical analysis. Statistical significance of the association testing was established using permutations. P-value |
Databáze: | OpenAIRE |
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