TY - JOUR
T1 - Gene × abstinence effects on drug cue reactivity in addiction
T2 - Multimodal evidence
AU - Moeller, Scott J.
AU - Parvaz, Muhammad A.
AU - Shumay, Elena
AU - Beebe-Wang, Nicasia
AU - Konova, Anna B.
AU - Alia-Klein, Nelly
AU - Volkow, Nora D.
AU - Goldstein, Rita Z.
PY - 2013
Y1 - 2013
N2 - Functional polymorphisms in the dopamine transporter gene (DAT1 or SLC6A3) modulate responsiveness to salient stimuli, such that carriers of one 9R-allele of DAT1 (compared with homozygote carriers of the 10R-allele) show heightened reactivity to drug-related reinforcement in addiction. Here, using multimodal neuroimaging and behavioral dependent variables in 73 human cocaine-addicted individuals and 47 healthy controls, we hypothesized and found that cocaine-addicted carriers of a 9R-allele exhibited higher responses to drug cues, but only among individuals who had used cocaine within 72 h of the study as verified by positive cocaine urine screens (a state characterized by intense craving). Importantly, this responsiveness to drug cues was reliably preserved across multimodal imaging and behavioral probes: psychophysiological event-related potentials, self-report, simulated cocaine choice, and fMRI. Because drug cues contribute to relapse, our results identify the DAT1R 9R-allele as a vulnerability allele for relapse especially during early abstinence (e.g., detoxification).
AB - Functional polymorphisms in the dopamine transporter gene (DAT1 or SLC6A3) modulate responsiveness to salient stimuli, such that carriers of one 9R-allele of DAT1 (compared with homozygote carriers of the 10R-allele) show heightened reactivity to drug-related reinforcement in addiction. Here, using multimodal neuroimaging and behavioral dependent variables in 73 human cocaine-addicted individuals and 47 healthy controls, we hypothesized and found that cocaine-addicted carriers of a 9R-allele exhibited higher responses to drug cues, but only among individuals who had used cocaine within 72 h of the study as verified by positive cocaine urine screens (a state characterized by intense craving). Importantly, this responsiveness to drug cues was reliably preserved across multimodal imaging and behavioral probes: psychophysiological event-related potentials, self-report, simulated cocaine choice, and fMRI. Because drug cues contribute to relapse, our results identify the DAT1R 9R-allele as a vulnerability allele for relapse especially during early abstinence (e.g., detoxification).
UR - http://www.scopus.com/inward/record.url?scp=84878872580&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.0695-13.2013
DO - 10.1523/JNEUROSCI.0695-13.2013
M3 - Article
C2 - 23761898
AN - SCOPUS:84878872580
SN - 0270-6474
VL - 33
SP - 10027
EP - 10036
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 24
ER -