Volume 81, Issue 5 p. 692-698
Article

A Genetic Variation in the Adenosine A2A Receptor Gene (ADORA2A) Contributes to Individual Sensitivity to Caffeine Effects on Sleep

J V Rétey,

Institute of Pharmacology and Toxicology, University of Zürich, Zürich, Switzerland

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M Adam,

Institute of Pharmacology and Toxicology, University of Zürich, Zürich, Switzerland

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R Khatami,

Institute of Pharmacology and Toxicology, University of Zürich, Zürich, Switzerland

Department of Neurology, University Hospital, Zürich, Switzerland

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U F O Luhmann,

Institute of Medical Genetics, University of Zürich, Zürich, Switzerland

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H H Jung,

Department of Neurology, University Hospital, Zürich, Switzerland

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W Berger,

Institute of Medical Genetics, University of Zürich, Zürich, Switzerland

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H-P Landolt,

Corresponding Author

Institute of Pharmacology and Toxicology, University of Zürich, Zürich, Switzerland

Zürich Center for Integrative Human Physiology (ZIHP), University of Zürich, Zürich, Switzerland

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First published: 28 February 2007
Citations: 3

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.

Clinical Pharmacology & Therapeutics (2007) 81, 692–698. doi:10.1038/sj.clpt.6100102; published online 28 February 2007