Is there a role for ADORA2A polymorphisms in levodopa-induced dyskinesia in Parkinson's disease patients?

M Rieck, AF Schumacher-Schuh… - …, 2015 - Future Medicine
Aim: Levodopa is first line treatment of Parkinson's disease (PD). However, its use is
associated with the presence of motor fluctuations and dyskinesias. In recent years …

[HTML][HTML] ADORA2A rs5760423 and CYP1A2 rs762551 Polymorphisms as Risk Factors for Parkinson's Disease

V Siokas, AM Aloizou, Z Tsouris, I Liampas… - Journal of Clinical …, 2021 - mdpi.com
Background: Parkinson's disease (PD) is the second commonest neurodegenerative
disease. The genetic basis of PD is indisputable. Both ADORA2A rs5760423 and CYP1A2 …

Mutation in ADORA1 identified as likely cause of early‐onset parkinsonism and cognitive dysfunction

E Jaberi, M Rohani, GA Shahidi, S Nafissi… - Movement …, 2016 - Wiley Online Library
Background We aimed to identify the genetic cause of neurological disease in an Iranian
family whose manifestations include symptoms of parkinsonism and cognitive dysfunction …

[HTML][HTML] The ADORA1 mutation linked to early-onset Parkinson's disease alters adenosine A1-A2A receptor heteromer formation and function

LI Sarasola, CL Del Torrent, A Pérez-Arévalo… - Biomedicine & …, 2022 - Elsevier
Adenosine modulates neurotransmission through inhibitory adenosine A 1 receptors (A 1
Rs) and stimulatory A 2A receptors (A 2A Rs). These G protein-coupled receptors are …

Coffee, ADORA2A, and CYP1A2: the caffeine connection in Parkinson's disease

RA Popat, SK Van Den Eeden… - European journal of …, 2011 - Wiley Online Library
Background and purpose: In 1‐methyl‐4‐phenyl 1, 2, 3, 6‐tetrahydropyridine animal models
of Parkinson's disease (PD), caffeine protects neurons by blocking the adenosine receptor …

[HTML][HTML] Analysis of ADORA2A rs5760423 and CYP1A2 rs762551 genetic variants in patients with Alzheimer's disease

V Siokas, DS Mouliou, I Liampas, AM Aloizou… - International Journal of …, 2022 - mdpi.com
Various studies have been conducted, exploring the genetic susceptibility of Alzheimer's
disease (AD). Adenosine receptor subtype A2a (ADORA2A) and cytochrome P450 1A2 …

[HTML][HTML] Adenosine A1-A2A receptor heteromer as a possible target for early-onset Parkinson's disease

V Fernández-Dueñas, A Pérez-Arévalo… - Frontiers in …, 2017 - frontiersin.org
Parkinson's disease (PD) is a progressive, neurodegenerative disorder that affects~ 1% of
individuals over the age of 60, which turns to 5% in subjects up to 85 years (de Lau and …

[HTML][HTML] Diagnostic prediction model for levodopa-induced dyskinesia in Parkinson's disease

BL Santos-Lobato, AF Schumacher-Schuh… - Arquivos de Neuro …, 2020 - SciELO Brasil
Background: There are currently no methods to predict the development of levodopa-
induced dyskinesia (LID), a frequent complication of Parkinson's disease (PD) treatment …

[HTML][HTML] Genetic Polymorphism of ADORA2A Is Associated With the Risk of Epilepsy and Predisposition to Neurologic Comorbidity in Chinese Southern Children

X Fan, Y Chen, W Li, H Xia, B Liu, H Guo… - Frontiers in …, 2020 - frontiersin.org
Epilepsy, a common disorder of the brain, exhibits a high morbidity rate in children.
Childhood epilepsy (CE) is frequently comorbid with neurologic and developmental …

DRD2 haplotype is associated with dyskinesia induced by levodopa therapy in Parkinson's disease patients

M Rieck, AF Schumacher-Schuh, V Altmann… - …, 2012 - Future Medicine
Aim: Dyskinesia and motor fluctuation are frequent and serious complications of chronic
levodopa therapy in patients with Parkinson's disease. Since genetic factors could play a …