Skip to main content
. Author manuscript; available in PMC: 2014 Nov 24.
Published in final edited form as: Psychopharmacology (Berl). 2010 Jun 9;211(3):245–257. doi: 10.1007/s00213-010-1900-1

Table 2.

Polymorphisms linked to acute and chronic response to caffeine

SNP Position Acute effects Long-term effects
CYP1A2
 rs762551 Intron I pos. 734: C → A Increased activity in smokers with A/A genotype (Sachse et al. 1999) Caffeine consumption does not appear to differ between the genotypes (Cornelis et al. 2007)
Risk of nonfatal myocardial infarction higher for subjects with C/C genotype (Cornelis et al. 2006)
No association found for risk of Parkinson’s disease (Facheris et al. 2008)
 rs35694136 No association found for risk of Parkinson’s disease (Facheris et al. 2008)
ADORA2A
 rs5751876 1976 C/T C/C genotype associated with greater caffeine sensitivity, sleep impairment, and increased beta activity during non-REM sleep (Retey et al. 2007)
T/T genotype associated with greater anxiety after caffeine (Alsene et al. 2003; Childs et al. 2008)
 rs35320474 2592 T/− T/T genotype associated with greater anxiety after caffeine (Childs et al. 2008) No association found for Parkinson’s disease or caffeine consumption (Tan et al. 2006)
 rs3032740 No association found for risk of Parkinson’s disease (Facheris et al. 2008)
DRD2
 rs1110976 Associated with greater levels of caffeine-induced anxiety (Childs et al. 2008)
COMT
 rs4680 Nucleotide codon 158: Val/Met Higher risk of acute myocardial infarction in alleles coding for low activity (Met/Met) (Happonen et al. 2006)