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Smit, D. J.

Publications and source records attributed to Smit, D. J..

3 recordsLinked to original sources

The Dynamics of Resting-State Alpha Oscillations Predict Individual Differences in Creativity

The neuronal mechanisms underlying creativity are poorly understood. Here, we investigated whether temporal dynamics of functional brain activity is a biomarker of creative ideation. Specifically, we investigated whether long-range temporal correlations in fluctuating resting-state alpha oscillations predict human creativity. Because lower temporal correlations reflect faster brain state switching, and faster state switching may be associated with increased flexibility of mind, we hypothesized that subjects with lower temporal correlations would show higher creativity. Creativity was measured by self-rating, examiner-rating and the alternative uses task in 40 healthy young adults, and scored on dimensions of verbal fluency, originality, elaboration, usefulness, and flexibility. For each dimension, the total number of subject-reported alternative uses that matched the criterium was noted (the quantity measure), as well as the proportion of uses that matched the dimensional criterium. A principal components analysis confirmed the two-component structure of quantity and quality. Eyes-open resting-state brain activity was measured by electroencephalogram (EEG) with 128 channels. Scaling exponents {beta} were derived from spectral analysis of the amplitude modulation of 8-13 Hz oscillations, where high exponents {beta} reflect lower decay of autocorrelation and slower switching of brain. Partial correlation analysis was used controlling for gender and age, and a cluster permutation test was performed correcting for multiple testing. Significant negative correlations between creativity and temporal correlations were observed, most prominent in right central/temporal brain areas. To our knowledge, this is the first demonstration that individual variation in the intrinsic dynamics of the brain may offer a neuronal explanation for individual variation in both the quality and quantity of creative ideation.

neuroscience↗

Genetic meta-analysis of obsessive-compulsive disorder and self-report compulsive symptoms.

We investigated whether obsessive compulsive (OC) symptoms from a population-based sample could be analyzed to detect genetic variants influencing OCD. We performed a GWAS on the obsession (rumination and impulsions) and compulsion (checking, washing, and ordering/precision) subscales of an abbreviated version of the Padua Inventory (N=8267 with genome-wide genotyping and phenotyping). The compulsion subscale showed a substantial and significant positive genetic correlation with an OCD case-control GWAS (rG=0.61, p=0.017) previously published by the Psychiatric Genomics Consortium (PGC-OCD). The obsession subscale and the total Padua score showed no significant genetic correlations (rG=-0.02 and rG=0.42, respectively). A meta-analysis of the compulsive symptoms GWAS with the PGC-OCD revealed no genome-wide significant SNPs (combined N=17992, indicating that the power is still low for individual SNP effects). A gene-based association analysis, however, yielded two novel genes (WDR7 and ADCK1). The top 250 genes in the gene-based test also showed significant increase in enrichment for psychiatric and brain-expressed genes. S-Predixcan testing showed that for genes expressed in hippocampus, amygdala, and caudate nucleus significance increased in the meta-analysis with compulsive symptoms compared to the original PGC-OCD GWAS. Thus, inclusion of dimensional symptom data in genome-wide association on clinical case-control GWAS of OCD may be useful to find genes for OCD if the data are based on quantitative indices of compulsive behavior. SNP-level power increases were limited, but aggregate, gene-level analyses showed increased enrichment for brain-expressed genes related to psychiatric disorders, and increased association with gene-expression in brain tissues with known emotional, reward processing, memory, and fear-formation functions.

genetics↗

Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity

Oscillations in neuronal activity are widely thought to play a crucial role in information processing and cortical communication 1-8. Brain oscillations have been widely investigated as biomarkers of psychiatric disorders and variation in normal human behavior 9, 10, including intelligence 11, 12, schizophrenia 13, 14, attentional deficits 15, 16, and substance use 17, 18. Beyond the biomarker, oscillatory activity may indeed cause variation in behavior, as it has been shown that disrupting oscillatory activity by blocking GABAergic fast-spiking interneurons in the frontal cortex of mice impairs behavioral flexibility8, consistent with ...

genetics↗