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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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CYP1A2 rs762551 and ADORA2A rs5760423 Polymorphisms in Patients with Blepharospasm

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Συγγραφέας
Siokas V., Kardaras D., Aloizou A.-M., Liampas I., Papageorgiou E., Drakoulis N., Tsatsakis A., Mitsias P.D., Hadjigeorgiou G.M., Tsironi E.E., Dardiotis E.
Ημερομηνία
2020
Γλώσσα
en
DOI
10.1007/s12031-020-01553-4
Λέξη-κλειδί
adenosine receptor
adenosine receptor subtype A2a
caffeine
cytochrome P450 1A2
unclassified drug
adenosine A2a receptor
ADORA2A protein, human
CYP1A2 protein, human
cytochrome P450 1A2
aged
Article
blepharospasm
clinical examination
cohort analysis
controlled study
DNA isolation
female
genetic polymorphism
genetic susceptibility
genetic variability
genotype
human
major clinical study
male
onset age
Parkinson disease
single nucleotide polymorphism
blepharospasm
genetics
middle aged
single nucleotide polymorphism
Aged
Blepharospasm
Cytochrome P-450 CYP1A2
Female
Humans
Male
Middle Aged
Polymorphism, Single Nucleotide
Receptor, Adenosine A2A
Humana Press Inc.
Εμφάνιση Μεταδεδομένων
Επιτομή
Blepharospasm (BSP) is a neurological movement disorder. Coffee consumption has been found to have a protective effect against BSP. BSP and apraxia of eyelid opening are particularly common among patients with PD. The CYP1A2 rs762551 and ADORA2A rs5760423 variants have been previously marginally associated with the risk of PD and are also implicated in caffeine metabolism pathways. The aim of the present study was to evaluate the effect of the CYP1A2 rs762551 and ADORA2A rs5760423 variants on BSP. A Southeastern European Caucasian (SEC) cohort of 206 BSP patients and 206 healthy controls was genotyped for rs762551 and rs5760423. CYP1A2 rs762551 was associated with a decreased BSP risk in the dominant (OR (95% CI) 0.62 (0.41–0.92), p = 0.017), log-additive (OR (95% CI) 0.68 (0.51–0.92), p = 0.011), and co-dominant modes (for the CC genotype OR (95% CI) 0.49 (0.25–0.93), p = 0.038). We provide preliminary evidence that CYP1A2 rs762551 is associated with BSP. Further studies and replication of our results are needed. © 2020, Springer Science+Business Media, LLC, part of Springer Nature.
URI
http://hdl.handle.net/11615/79038
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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