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A genetic variation in the adenosine A2A receptor gene (ADORA2A) contributes to individual sensitivity to caffeine effects on sleep.
- Source :
-
Clinical pharmacology and therapeutics [Clin Pharmacol Ther] 2007 May; Vol. 81 (5), pp. 692-8. Date of Electronic Publication: 2007 Feb 28. - Publication Year :
- 2007
-
Abstract
- Caffeine is the most widely used stimulant in Western countries. Some people voluntarily reduce caffeine consumption because it impairs the quality of their sleep. Studies in mice revealed that the disruption of sleep after caffeine is mediated by blockade of adenosine A2A receptors. Here we show in humans that (1) habitual caffeine consumption is associated with reduced sleep quality in self-rated caffeine-sensitive individuals, but not in caffeine-insensitive individuals; (2) the distribution of distinct c.1083T>C genotypes of the adenosine A2A receptor gene (ADORA2A) differs between caffeine-sensitive and -insensitive adults; and (3) the ADORA2A c.1083T>C genotype determines how closely the caffeine-induced changes in brain electrical activity during sleep resemble the alterations observed in patients with insomnia. These data demonstrate a role of adenosine A2A receptors for sleep in humans, and suggest that a common variation in ADORA2A contributes to subjective and objective responses to caffeine on sleep.
- Subjects :
- Adult
Aged
Alleles
DNA genetics
Data Interpretation, Statistical
Electroencephalography drug effects
Female
Genetic Variation
Genotype
Humans
Internet
Male
Middle Aged
Polysomnography drug effects
Reverse Transcriptase Polymerase Chain Reaction
Surveys and Questionnaires
Caffeine pharmacology
Central Nervous System Stimulants pharmacology
Receptor, Adenosine A2A genetics
Receptor, Adenosine A2A physiology
Sleep drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 0009-9236
- Volume :
- 81
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Clinical pharmacology and therapeutics
- Publication Type :
- Academic Journal
- Accession number :
- 17329997
- Full Text :
- https://doi.org/10.1038/sj.clpt.6100102