Shared neurogenetic substrates of nonplanning impulsivity and procrastination.
other · Level V
Where this comes from
- Record sourced from PubMed, PMID 42412943.
- Also identified by DOI 10.1073/pnas.2605127123.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Procrastination has a maladaptive impact on health and survival, yet it remains moderately heritable, presenting a biological paradox. Procrastination has been conceptualized as a byproduct of impulsivity, explaining its prevalence despite no discernible adaptive benefit. However, their shared neurobiological substrates have yet to be elucidated. Using a longitudinal twin cohort (<i>N</i> = 154), we show that nonplanning impulsivity (NPI) during late adolescence and early adulthood is prospectively associated with procrastination in later life. This effect was independently replicated in two cross-sectional cohorts (<i>N</i> = 327; <i>N</i> = 1,543). Twin modeling using an additive genetic and nonshared environmental (AE) framework, together with a meta-analysis of twin studies (<i>N</i> = 3,656 twin pairs), revealed significant shared genetic contributions (<i>r<sub>g</sub></i> = 0.51). Beyond genetic overlap, neuroimaging meta-analysis (<i>NeuroSynth</i> meta-analysis for impulsivity: <i>k</i> = 198 studies, 5855 loci; mini meta-analysis for procrastination: <i>k</i> = 5 studies, 7 independent samples, <i>N<sub>cumulative</sub></i> = 893 participants), normative modeling (<i>N</i> = 37,407), and seed-based <i>d</i> mapping (SDM) converged on the left dorsolateral prefrontal cortex (DLPFC) as the region of maximal overlap between NPI and procrastination. The transcriptional profiles of the left DLPFC and impulsivity-associated genes exhibited functional convergence on regulation of biological and cellular processes. These genes showed brain-specific expression and associations with cortical metabolism, neurodegenerative disease, and developmental expression peaks, indicating a shared molecular basis for the neurogenetic architecture of procrastination. Together, our findings delineate a cross-scale characterization of the shared neurogenetic substrates linking NPI and procrastination, offering empirical evidence that elucidates the biological origins of procrastination.
Medical subject headings
- Impulsive Behavior
- Procrastination