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Daviet, R.

Publications and source records attributed to Daviet, R..

2 recordsLinked to original sources

Multimodal brain imaging study of 19,825 participants reveals adverse effects of moderate drinking

Heavy alcohol consumption can have significant deleterious neural consequences, including brain atrophy, neuronal loss, poorer white matter fiber integrity, and cognitive decline. However, the effects of light-to-moderate alcohol consumption on brain structure remain unclear. Here, we examine the associations between alcohol intake and brain structure using multimodal imaging data from 36,678 generally healthy middle-aged and older adults from the UK Biobank, controlling for numerous potential confounds. We find negative associations between alcohol intake and global gray matter volume (GMV) and white matter volume (WMV), which become stronger as intake increases. An examination of the associations between alcohol intake and 139 regional GMV imaging-derived phenotypes (IDPs) and 375 WM microstructure IDPs yielded 304 (59.1%) significant findings, including 125 GMV IDPs that are spread across the brain and 179 WM microstructure IDPs across multiple tract regions. In general, findings comport with the existing literature. However, a daily alcohol intake of as little as one to two units - 250 to 500 ml of a 4% beer or 76 to 146 ml of a 13% wine - is already associated with GMV deficits and altered WMV microstructure, placing moderate drinkers at risk. One Sentence SummaryModerate alcohol intake, consuming one or more daily alcohol units, has adverse effects on brain health.

neuroscience

Genetic Underpinnings of Risky Behavior Relate to Altered Neuroanatomy

Previous research points to the heritability of risk-taking behaviour. However, evidence on how genetic dispositions are translated into risky behaviour is scarce. Here, we report a genetically-informed neuroimaging study of real-world risky behaviour across the domains of drinking, smoking, driving, and sexual behaviour, in a European sample from the UK Biobank (N= 12,675). We find negative associations between risky behaviour and grey matter volume (GMV) in distinct brain regions, including amygdala, ventral striatum, hypothalamus, and dorsolateral prefrontal cortex (dlPFC). These effects replicate in an independent sample recruited from the same population (N=13,004). Polygenic risk scores for risky behaviour, derived from a genome-wide association study in an independent sample (N=297,025), are inversely associated with GMV in dlPFC, putamen, and hypothalamus. This relation mediates ~2.2% of the association between genes and behaviour. Our results highlight distinct heritable neuroanatomical features as manifestations of the genetic propensity for risk taking. One Sentence SummaryRisky behaviour and its genetic associations are linked to less grey matter volume in distinct brain regions.

neuroscience