DRD2, dopamine receptor D2, 1813

N. diseases: 437; N. variants: 42
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE The importance of dopamine D2 receptors (DRD2) for central nervous dopaminergic signalling makes variants in the DRD2 gene potential modulators of the risk or course of various behavioural, psychiatric or neurologic diseases (e.g. addiction, schizophrenia, Parkinson's disease). 19512960 2009
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Association of the DRD2 and DRD3 polymorphisms with response to pramipexole in Parkinson's disease patients. 19396436 2009
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE This study identified apomorphine use and levodopa dosages between 500 and 1000 mg as non-genetic and the 15× DRD2 CA repeat allele as genetic determinants for the discontinuation of non-ergoline DA treatment in patients with PD. 19669131 2009
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Among non-Hispanic whites, homozygous carriers of Taq1A DRD2 (rs1800497) polymorphism had an increased risk of PD compared to homozygous wildtype carriers (OR=1.5, 95% CI 1.0-2.3). 21663922 2011
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE The DRD2 rs1800497 and DRD4 rs1800955 polymorphisms showed no association with PD. 21781348 2011
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Since genetic factors could play a role in determining the occurrence of these problems, the aim of the present study was to investigate whether possible functional polymorphisms among DRD2 and ANKK1 genes are associated with the risk of developing dyskinesia and motor fluctuations in Parkinson's disease patients. 23171335 2012
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE We assessed whether allelic variants of dopamine D2 receptors (DRD2), catechol-O-methyltransferase (COMT) and dopamine transporter (DAT) were associated with the development of ICDs in PD. 22113132 2012
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Antipsychotics and serotoninergic antidepressants may potentially attenuate PD risk, and lithium and bupropion may augment risk, through MAPT, GBA, CCDC62, HIP1R, BDNF, and DRD2 transcription, with MAPT, GBA, and CCDC62 being strongly associated with PD risk in recent meta-analyses. 22507762 2012
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE In the current study, we determined whether a dopamine D2 receptor DNA sequence polymorphism interacts with L-DOPA during motor tasks in patients with Parkinson's disease (PD). 23439215 2013
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE We examined the relation between inhibitory ability (measured by the Stop Signal Task) and polymorphisms of COMT Val158Met and DRD2 C957T in patients with idiopathic PD. 24749760 2014
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE Pharmacological modulation of A2ARs is particularly useful in Parkinson's disease (PD) due to their property of antagonizing dopamine D2 receptor activity. 24892887 2014
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE The DRD3 (rs6280) polymorphism, but not DRD2 (Taq1A) or GRIN2B, influences younger PD age of onset in the US Caucasian population. 26627941 2016
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Single nucleotide polymorphisms, rs2283265 and rs1076560, in the dopamine D2 receptor gene (DRD2) were found to be significantly associated with a favourable peak response to rasagiline at 12 weeks in early Parkinson's disease after controlling for multiple testing. 27190009 2016
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE In conclusion, we suggest that L-DOPA may attenuate the neuropathology of PD by regulating signaling related to DRD2 in neuronal cells under α-syn-induced toxicity. 28687316 2017
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE To investigate the association between Dopamine receptor D type 2 (DRD2) dinucleotide short tandem repeat (CA<sub>n</sub>-STR) and Dopamine receptor D type 3 (DRD3) Ser9Gly polymorphisms and the risk of PD, as well as the possible reasons for PD patients using different doses of DAs, we recruited 168 idiopathic PD patients and 182 controls. 27817855 2017
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE The aim of this study was to investigate the topographical distribution of dopamine transporter (DAT), dopamine D2 receptor, and glucose metabolism in Parkinson's disease (PD) using PET/computed tomography (CT) scanning and statistical parametric mapping (SPM) analysis. 27893588 2017
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Human genetic studies also show a significant association of DRD2 polymorphisms with disorders including schizophrenia and Parkinson's disease. 29107444 2017
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE The changes in expression at the mRNA and protein levels suggest that Snca may be involved in neurodegeneration and Drd2 may participate in the development of the compensatory mechanisms in the early stages of PD pathogenesis. 27757834 2017
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE The D2 dopamine receptor (DRD2) is the primary target for both typical and atypical antipsychotic drugs, and for drugs used to treat Parkinson's disease. 29466326 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Dopamine D2 receptor-mediated neuroprotection in a G2019S Lrrk2 genetic model of Parkinson's disease. 29434188 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE In the present study, we used 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced PD mouse model to investigate whether Drd2 could suppress astrocytic NLRP3 inflammasome activation. 29786071 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE The poorer cognitive performance in DRD2 <sup>957</sup> T/T carriers with PD occurred mainly in episodic memory and attention. 28869277 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE To determine whether dopaminergic (rs1076560 DRD2 G > T and rs4680 catechole-o-methyltranspherase (COMT) Val158Met) or brain derived neurotrophic factor (rs6265 BDNF Val66Met) genetic polymorphisms are associated with gait function and medication responsiveness in Parkinson's disease. 29249680 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Dopamine D2 receptor activation potently inhibits striatal glutamatergic transmission in a G2019S LRRK2 genetic model of Parkinson's disease. 29908325 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE Our study illustrates that astrocytic Drd2 inhibits neuroinflammation through a β-arrestin2-dependent mechanism and provides a new strategy for treatment of PD. 30200997 2018