Alcohol use and brain morphology in adolescence: A longitudinal study in three different cohorts

Alcohol consumption is commonly initiated during adolescence, but the effects on human brain development remain unknown. In this multisite study, we investigated the longitudinal associations of adolescent alcohol use and brain morphology. Three longitudinal cohorts in the Netherlands (BrainScale n ...

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Published in:The European journal of neuroscience Vol. 54; no. 6; pp. 6012 - 6026
Main Authors: El Marroun, Hanan, Klapwijk, Eduard T., Koevoets, Martijn, Brouwer, Rachel M., Peters, Sabine, van't Ent, Dennis, Boomsma, Dorret I., Muetzel, Ryan L., Crone, Eveline A., Hulshoff Pol, Hilleke E., Franken, Ingmar H. A.
Format: Journal Article
Language:English
Published: Chichester Wiley Subscription Services, Inc 01-09-2021
John Wiley and Sons Inc
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Summary:Alcohol consumption is commonly initiated during adolescence, but the effects on human brain development remain unknown. In this multisite study, we investigated the longitudinal associations of adolescent alcohol use and brain morphology. Three longitudinal cohorts in the Netherlands (BrainScale n = 200, BrainTime n = 239 and a subsample of the Generation R study n = 318) of typically developing participants aged between 8 and 29 years were included. Adolescent alcohol use was self‐reported. Longitudinal neuroimaging data were collected for at least two time points. Processing pipelines and statistical analyses were harmonized across cohorts. Main outcomes were global and regional brain volumes, which were a priori selected. Linear mixed effect models were used to test main effects of alcohol use and interaction effects of alcohol use with age in each cohort separately. Alcohol use was associated with adolescent's brain morphology showing accelerated decrease in grey matter volumes, in particular in the frontal and cingulate cortex volumes, and decelerated increase in white matter volumes. No dose–response association was observed. The findings were most prominent and consistent in the older cohorts (BrainScale and BrainTime). In summary, this longitudinal study demonstrated differences in neurodevelopmental trajectories of grey and white matter volume in adolescents who consume alcohol compared with non‐users. These findings highlight the importance to further understand underlying neurobiological mechanisms when adolescents initiate alcohol consumption. Therefore, further studies need to determine to what extent this reflects the causal nature of this association, as this longitudinal observational study does not allow for causal inference. Alcohol consumption is often initiated during adolescence, a period of rapid brain development. This multisite cohort study showed that adolescent alcohol use in was associated with grey matter volume reductions over time, particularly in the frontal and cingulate cortex. Future studies should unravel mechanisms underlying these associations as observational studies do not allow for causal inference. This graphical has been designed using resources from flaticon.com
Bibliography:Funding information
Eduard T. Klapwijk and Martijn Koevoets contributed equally to this work.
Edited by: Dr. John Foxe
Brain and Behavior Research Foundation: NARSAD Young Investigator Grant, Grant/Award Number: 27853; European Research Council, Grant/Award Number: ERC‐2010‐StG‐263234, ERC‐230374; Dutch Brain Foundation (Hersenstichting), Grant/Award Number: GH2016.2.01; Nederlandse Organisatie voor Wetenschappelijk Onderzoek, Grant/Award Numbers: 51.02.061, 51.02.062, 480‐04‐004, 433‐09‐220, 56‐464‐14192, 480‐15‐001/674; Stichting Volksbond Rotterdam; University Utrecht (High Potential Grant); Neuroscience Campus Amsterdam; European Union’s Horizon 2020 research and innovation programme (grant agreement No.733206 LifeCycle)
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Funding information Brain and Behavior Research Foundation: NARSAD Young Investigator Grant, Grant/Award Number: 27853; European Research Council, Grant/Award Number: ERC‐2010‐StG‐263234, ERC‐230374; Dutch Brain Foundation (Hersenstichting), Grant/Award Number: GH2016.2.01; Nederlandse Organisatie voor Wetenschappelijk Onderzoek, Grant/Award Numbers: 51.02.061, 51.02.062, 480‐04‐004, 433‐09‐220, 56‐464‐14192, 480‐15‐001/674; Stichting Volksbond Rotterdam; University Utrecht (High Potential Grant); Neuroscience Campus Amsterdam; European Union’s Horizon 2020 research and innovation programme (grant agreement No.733206 LifeCycle)
ISSN:0953-816X
1460-9568
DOI:10.1111/ejn.15411