CYP2A6 Genetic Variation Alters Striatal-Cingulate Circuits, Network Hubs, and Executive Processing in Smokers
Variation in the CYP2A6 gene alters the rate of nicotine metabolic inactivation and is associated with smoking behaviors and cessation success rates. The underlying neurobiological mechanisms of this genetic influence are unknown. Intrinsic functional connectivity strength, a whole-brain, data-drive...
Saved in:
Published in | Biological psychiatry (1969) Vol. 81; no. 7; pp. 554 - 563 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.04.2017
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Variation in the CYP2A6 gene alters the rate of nicotine metabolic inactivation and is associated with smoking behaviors and cessation success rates. The underlying neurobiological mechanisms of this genetic influence are unknown.
Intrinsic functional connectivity strength, a whole-brain, data-driven, graph theory–based method, was applied to resting-state functional magnetic resonance imaging data in 66 smokers and 92 nonsmokers. A subset of subjects (n = 23/20; smokers/nonsmokers) performed the monetary incentive delay task, probing reward anticipation, and a go/no-go task, probing response inhibition, on two occasions, in the presence and absence of a nicotine patch.
A significant CYP2A6 genotype × smoking effect was found in the dorsal anterior cingulate cortex and ventral striatum, such that the normal (vs. slow) genotype individuals showed greater functional connectivity strength among smokers but not nonsmokers. Functional connectivity strength was negatively associated with severity of nicotine dependence in slow metabolizers. Both hubs were biased by inputs from the insula identified from seed-based connectivity. Similar gene × environment interactions were seen in ventral striatum during smoking abstinence when subjects performed the monetary incentive delay task and in dorsal anterior cingulate cortex when they performed the go/no-go task; both reductions were “normalized” in smokers (and increased in nonsmokers) after acute nicotine administration.
Because the CYP2A6 effect was seen only in smokers, these data suggest that the rate of nicotine metabolism—and thus the concentration of nicotine presented to the brain over the course of nicotine addiction—shapes brain circuits that, among other functions, compute reward and impulsivity processes. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Yihong Yang, yihongyang@intra.nida.nih.gov, 251 Bayview Blvd, Suite 200, Baltimore, MD 21224 Sufang Li, sufang.li@nih.gov, 251 Bayview Blvd, Suite 200, Baltimore, MD 21224 Rachel F. Tyndale, r.tyndale@utoronto.ca, Tel: (416)978-6374 Fax: (416)978-6395, Room 4326, 1 King’s College Circle, Toronto, ON, M5S 1A8 Canada Ewa Hoffmann, e.hoffmann@utoronto.ca, Room 4326, 1 King’s College Circle, Toronto, ON, M5S 1A8 Canada |
ISSN: | 0006-3223 1873-2402 1873-2402 |
DOI: | 10.1016/j.biopsych.2016.09.013 |