Binge drinking trajectory and neuropsychological functioning among university students: A longitudinal study

Abstract Background Adolescence is a time of considerable neurodevelopment. Binge drinking (BD) during this period increases the vulnerability to its neurotoxic effects. This longitudinal study aimed to investigate the relationship between BD trajectory over university years and neuropsychological f...

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Veröffentlicht in:Drug and alcohol dependence 2013-11, Vol.133 (1), p.108-114
Hauptverfasser: Mota, Nayara, Parada, María, Crego, Alberto, Doallo, Sonia, Caamaño-Isorna, Francisco, Rodríguez Holguín, Socorro, Cadaveira, Fernando, Corral, Montserrat
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Sprache:eng
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Zusammenfassung:Abstract Background Adolescence is a time of considerable neurodevelopment. Binge drinking (BD) during this period increases the vulnerability to its neurotoxic effects. This longitudinal study aimed to investigate the relationship between BD trajectory over university years and neuropsychological functioning. Methods Cohort-study. Two-year follow-up. A total of 89 university students were assessed: 40 Non-BD (at Initial and Follow-up), 16 Ex-BD (BD at Initial but not at Follow-up) and 33 BD (at both times). Neuropsychological assessment of working memory, episodic memory and executive abilities was carried out during their first (Initial) and third (Follow-up) academic year at the University of Santiago de Compostela. Results BD subjects performed less well on the Wechsler Memory Scale-III (WMS-III) Logical Memory Subtest (immediate theme recall, P = .034; delayed theme recall, P = .037; and percent retention, P = .035) and committed more perseverative errors on the Self-Ordered Pointing Task (SOPT) ( P = .021) than Non-BD. There were no differences between Ex-BD and Non-BD. Conclusions Binge drinking trajectory during adolescence is associated with neuropsychological performance. Persistent BD, but not Ex-BD, is associated with verbal memory and monitoring difficulties. This is compatible with the hypothesis that heavy alcohol use during adolescence may affect cognitive functions that rely on the temporomesial and dorsolateral prefrontal cortex.
ISSN:0376-8716
1879-0046
DOI:10.1016/j.drugalcdep.2013.05.024