TY - JOUR
T1 - AKTI Moderation of Cannabis-Induced Cognitive Alterations in Psychotic Disorder
AU - van Winkel, Ruud
AU - van Beveren, Nico J. M.
AU - Genetic Risk and Outcome of Psychosis (GROUP) Investigators
AU - van Os, Jim
AU - Simons, Claudia
PY - 2011/11
Y1 - 2011/11
N2 - Genetic variation in AKTI may be associated with sensitivity to the psychotomimetic effects of cannabis as well as with increased risk for psychotic disorder following cannabis use. Investigation of the effect of this interaction on relevant intermediate phenotypes for psychosis, such as cognition, may help to clarify the underlying mechanism. Thus, verbal memory (visually presented Word Learning Task), sustained attention (Continuous Performance Test, CPT), AKTI rs2494732 genotype, and cannabis use were examined in a large cohort of patients with psychotic disorder. No evidence was found for AKTI x cannabis interaction on verbal memory. Cannabis use preceding onset of psychotic disorder did interact significantly with AKTI rs2494732 genotype to affect CPT reaction time (beta = 8.0, SE 3.9, p = 0.037) and CPT accuracy (beta = -1.2, SE 0.4, p = 0.003). Cannabis-using patients with the a priori vulnerability C/C genotype were slower and less accurate on the CPT, whereas cannabis-using patients with the T/T genotype had similar or better performance than non-using patients with psychotic disorder. The interaction was also apparent in patients with psychotic disorder who had not used cannabis in the 12 months preceding assessment, but was absent in the unaffected siblings of these patients and in healthy controls. In conclusion, cannabis use before onset of psychosis may have long-lasting effects on measures of sustained attention, even in the absence of current use, contingent on AKTI rs2494732 genotype. The results suggest that long-term changes in cognition may mediate the risk-increasing effect of the AKTI x cannabis interaction on psychotic disorder. Neuropsychopharmacology (2011) 36, 2529-2537; doi:10.1038/npp.2011.141; published online 20 July 2011
AB - Genetic variation in AKTI may be associated with sensitivity to the psychotomimetic effects of cannabis as well as with increased risk for psychotic disorder following cannabis use. Investigation of the effect of this interaction on relevant intermediate phenotypes for psychosis, such as cognition, may help to clarify the underlying mechanism. Thus, verbal memory (visually presented Word Learning Task), sustained attention (Continuous Performance Test, CPT), AKTI rs2494732 genotype, and cannabis use were examined in a large cohort of patients with psychotic disorder. No evidence was found for AKTI x cannabis interaction on verbal memory. Cannabis use preceding onset of psychotic disorder did interact significantly with AKTI rs2494732 genotype to affect CPT reaction time (beta = 8.0, SE 3.9, p = 0.037) and CPT accuracy (beta = -1.2, SE 0.4, p = 0.003). Cannabis-using patients with the a priori vulnerability C/C genotype were slower and less accurate on the CPT, whereas cannabis-using patients with the T/T genotype had similar or better performance than non-using patients with psychotic disorder. The interaction was also apparent in patients with psychotic disorder who had not used cannabis in the 12 months preceding assessment, but was absent in the unaffected siblings of these patients and in healthy controls. In conclusion, cannabis use before onset of psychosis may have long-lasting effects on measures of sustained attention, even in the absence of current use, contingent on AKTI rs2494732 genotype. The results suggest that long-term changes in cognition may mediate the risk-increasing effect of the AKTI x cannabis interaction on psychotic disorder. Neuropsychopharmacology (2011) 36, 2529-2537; doi:10.1038/npp.2011.141; published online 20 July 2011
KW - cannabinoids
KW - cognition
KW - schizophrenia/antipsychotics
KW - neurogenetics
KW - AKTI
KW - cannabis
U2 - 10.1038/npp.2011.141
DO - 10.1038/npp.2011.141
M3 - Article
C2 - 21775978
SN - 0893-133X
VL - 36
SP - 2529
EP - 2537
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 12
ER -