Cognitive control is fundamental to goal-directed behavior, and its protracted maturation is a hallmark of adolescent brain development. In adulthood, the inferior frontal junction (IFJ) is functionally characterized as a critical region for updating task representations to guide the implementation of cognitive control. Yet, how its domain-general control functions emerge and mature across development remains largely underexplored. Specifically, it is unclear whether the IFJs capacity for cognitive control enhances uniformly as a single construct, or if this region matures asynchronously for distinct control processes like inhibition, switching, and working memory. To address this gap, we conducted a combined systematic review and coordinate-based neuroimaging meta-analysis. Applying multilevel kernel density analyses to fMRI studies of inhibition, switching, and working memory in youth and adults, we synthesized data from 72 contrasts (779 foci; N = 1,913). The results revealed a staggered developmental trajectory for IFJ recruitment. While adults showed consistent convergence of activation in the IFJ across all three domains, youth exhibited robust bilateral IFJ convergence exclusively during inhibitory control tasks. This suggests inhibition may be a developmentally foundational process localized to this region earlier in the lifespan. Furthermore, adults demonstrated hemispheric specialization absent in youth: left IFJ was uniquely sensitive to switching and working memory in adults, but not in youth. Together, these findings support a model where the IFJ does not mature as a static, monolithic node, but rather acts as a dynamic hub that integrates fractionated cognitive processes at different stages of development.
Disclosure in the era of generative artificial intelligence
Generative artificial intelligence (AI) has rapidly become embedded in academic writing, assisting with tasks ranging from language editing to drafting text and producing evidence. Despite