This research was supported by the NIH grants DA 005147, DA 013240, DA 024417, and AA 09367. The first author's effort on this project was supported by T32 grant MH017069 from the National Institute of Mental Health. Special thanks to Steve Malone for helping with data processing and analysis.
P300 amplitude reduction is associated with early-onset and late-onset pathological substance use in a prospectively studied cohort of 14-year-old adolescents
Article first published online: 2 AUG 2013
Copyright © 2013 Society for Psychophysiological Research
Volume 50, Issue 10, pages 974–982, October 2013
How to Cite
Perlman, G., Markin, A. and Iacono, W. G. (2013), P300 amplitude reduction is associated with early-onset and late-onset pathological substance use in a prospectively studied cohort of 14-year-old adolescents. Psychophysiology, 50: 974–982. doi: 10.1111/psyp.12081
- Issue published online: 23 SEP 2013
- Article first published online: 2 AUG 2013
- Manuscript Accepted: 20 MAY 2013
- Manuscript Received: 30 JAN 2013
- NIH. Grant Numbers: DA 005147, DA 013240, DA 024417, AA 09367
- National Institute of Mental Health. Grant Number: MH017069
- Individual differences
P3 amplitude reduction (P3AR) is associated with risk for adolescent-onset pathological substance use (PSU). In this longitudinal study, data from over 1,100 adolescent twins were used to examine P3AR in relation to early adolescent onset PSU (i.e., by age 14), late adolescent onset PSU (i.e., ages 14–18), misuse of different classes of substances (PSU-nicotine, PSU-alcohol, PSU-illicit), degree of PSU comorbidity, and gender differences. P3 amplitude was recorded at age 14 from two midline electrodes during a visual oddball paradigm. PSU was defined as meeting criteria for any symptom of a substance use disorder assessed using semistructured clinical interviews. P3AR was associated with degree of drug class comorbidity, early adolescent onset PSU for all three substance classes, and late adolescent onset PSU for alcohol and illicit PSU. Gender differences in P3AR were not statistically significant. These findings provide further evidence that P3AR indexes a nonspecific diathesis for adolescent-onset PSU.