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Chuan-Peng, H.

Publications and source records attributed to Chuan-Peng, H..

3 recordsLinked to original sources

Shared brain basis for altered self-referential processing across psychiatric disorders? A systematic review and meta-analysis of neuroimaging studies

Self-referential processing is a fundamental cognitive function, and abnormalities in its neural implementation have been reported across a range of psychiatric disorders, leading to the proposal that such alterations may constitute a transdiagnostic neurobiological feature. Yet claiming transdiagnostic requires rigorous evidence. Here, we examined the evidence for such a hypothesis by conducting a systematic review and coordinate-based meta-analysis of psychiatric neuroimaging studies that employed self-referential tasks. The systematic review identified 36 neuroimaging studies across 9 broad categories of psychiatric disorders, suggesting that the neural aberrancy of self-referential processing is indeed of great interest across different diagnosis. Of these, 27 studies were eligible for the ALE meta-analysis. The ALE results revealed hypoactivation of the right precuneus in psychiatric groups relative to health controls, alongside hyperactivation of the right triangular part of the inferior frontal gyrus (IFGtri) during self-referential processing in psychiatric groups. Notably the precuneus and IFGtri are core nodes of the default mode network and the frontal-parietal control network, respectively, suggesting that aberrant self-referential processing across psychiatric disorders may be characterized by disrupted default mode network engagement accompanied by compensatory or maladaptive recruitment of control-related frontal regions. Together, our findings revealed a strong research interest in neural aberrancy of self-referential processing as a transdiagnostic feature. However, available evidence only provided preliminary evidence for such statement. To move forward, the field needs coordinated efforts to systematically accumulate data and collecting new datasets.

neuroscience↗

A ventral striatal learning signal reflecting individual differences in the success of fear extinction

Individual differences in fear extinction learning are centrally involved in anxiety vulnerability. We here investigate individual extinction differences using a model-free, data-driven approach, by applying Latent Class Growth Modeling (LCGM) to four in-house data sets from altogether N=234 healthy male participants. This revealed two distinct trajectory classes: fast extinguishers and slow extinguishers. This pattern was replicated in two independent public data sets (total N=275, female and male). In a subset of the in-house samples with functional magnetic resonance imaging (fMRI) data (n=122 males), we investigated the neural correlates of class membership, focusing on the ventral striatum (VS), a key area previously implicated in encoding extinction prediction errors (EPE). We found that fast extinguishers exhibited VS activity at the time of unconditioned stimulus omission early in extinction, consistent with an EPE signal, whereas this signal only appeared late in extinction in slow extinguishers. These findings suggest that extinction success is shaped by how the VS learns safety.

neuroscience↗

Arousal defines the conditions for facilitation by L-DOPA of extinction consolidation and associated prefrontal activity

Even after successful extinction, conditioned fear can return. Strengthening the consolidation of the fear-inhibitory safety memory formed during extinction is one way to counteract return of fear. In this preregistered direct replication study in male participants, we confirm that spontaneous post-extinction reactivations of a neural activation pattern evoked in the ventromedial prefrontal cortex (vmPFC) during extinction predict extinction memory retrieval 24 h later. We do not confirm that L-DOPA administration after extinction enhances retrieval and that this is mediated by enhancement of the number of vmPFC reactivations. However, additional non-preregistered analyses reveal a beneficial effect of L-DOPA on extinction retrieval when controlling for the trait-like stable baseline levels of salivary alpha-amylase enzymatic activity (trait sAA) levels that participants show on the three experimental days. Further, trait sAA negatively predicts retrieval, and this effect is rescued by L-DOPA treatment. Our results suggest that individuals with high basal levels of sympathetic nervous system (SNS) activity may have poor extinction and that L-DOPA may be selectively beneficial for these individuals, which holds potential for clinical applications.

neuroscience↗