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VanTieghem, M.

Publications and source records attributed to VanTieghem, M..

2 recordsLinked to original sources

Spontaneous reinstatement of episodic memories in the developing human brain

Starting early in development, the hippocampus can support the formation of episodic memories, and yet how the developing brain stabilizes these memories to support their long-term accessibility has not been established. This study (N = 49; mean age = 11.68 years) examined how encoded episodic memories are stabilized in development. Using fMRI and multivariate analyses, we tracked neural reinstatement of newly learned item-location-context associations in youth. During encoding, hippocampus and visual cortex activity predicted later memory success. Crucially, during post-encoding rest, spontaneous pattern reinstatement in the angular gyrus and the pregenual medial prefrontal cortex (mPFC) also predicted memory, with age-related changes in the mPFC and superior frontal gyrus. These findings suggest that episodic memory stabilization during childhood and adolescence is broadly supported by developmental change within regions associated with mature function, advancing our understanding of how different memory stages contribute to how we learn and remember across the lifespan.

neuroscience↗

Age-related change in task-evoked amygdala-prefrontal circuitry: a multiverse approach with an accelerated longitudinal cohort aged 4-22 years

The amygdala and its connections with medial prefrontal cortex (mPFC) play central roles in the development of emotional processes. While several studies have suggested that this circuitry exhibits functional changes across the first two decades of life, findings have been mixed - perhaps resulting from differences in analytic choices across studies. Here we used multiverse analyses to examine the robustness of task-based amygdala-mPFC function findings to analytic choices within the context of an accelerated longitudinal design (4-22 years- old; N=98; 183 scans; 1-3 scans/participant). Participants, recruited from the greater Los Angeles area, completed an event-related emotional face (fear, neutral) task. Parallel analyses varying in preprocessing and modeling choices found that age-related change estimates for amygdala reactivity were more robust than task-evoked amygdala-mPFC functional connectivity to varied analytical choices. Specification curves indicated evidence for age-related decreases in amygdala reactivity to faces, though within-participant changes in amygdala reactivity could not be differentiated from between-participant differences. In contrast, amygdala--mPFC functional connectivity results varied across methods much more, and evidence for age-related change in amygdala-mPFC connectivity was not consistent. Generalized psychophysiological interaction (gPPI) measurements of connectivity were especially sensitive to whether a deconvolution step was applied. Our findings demonstrate the importance of assessing the robustness of findings to analysis choices, although the age-related changes in our current work cannot be overinterpreted given low test-retest reliability. Together, these findings highlight both the challenges in estimating developmental change in longitudinal cohorts and the value of multiverse approaches in developmental neuroimaging for assessing robustness of results. (Preprint: https://www.biorxiv.org/content/10.1101/2021.10.08.463601v1). Key PointsO_LIMultiverse analyses applied to fMRI data are valuable for determining the robustness of findings to varied analytical choices C_LIO_LIIn the current study, age-related change estimates for amygdala reactivity were relatively robust to analytical decisions, though gPPI functional connectivity analyses were much more sensitive, leading some estimates to flip sign C_LIO_LIBoth test-retest reliability and robustness to analytical choices are important considerations for developmental research C_LI

neuroscience↗