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Wojciechowski, J.

Publications and source records attributed to Wojciechowski, J..

6 recordsLinked to original sources

Compensatory Mechanisms in Visual Sequence Learning: An fMRI Study of Children with Developmental Language Disorder

Symptoms of developmental language disorder (DLD) may in part result from an underlying deficit in statistical learning (SL). This learning deficit may be related to the ability to extract probabilistic properties of events in the environment, which is based on the functions of cortical and subcortical brain regions underlying SL. Using a behavioral SL task and functional magnetic resonance imaging (fMRI), we tested SL ability in the visual domain and its neural correlates in children with DLD and their typically developing (TD) peers. During fMRI, children performed SL tasks involving sequences of two types of stimuli: easy-to-name (EN) objects and difficult-to-name (DN) objects. The children underwent a pre-training fMRI, one week of behavioural training and a post-training fMRI. Similar task performance was observed in both groups during the experimental sessions, with an improvement in performance following training in the SL tasks involving both EN and DN objects. FMRI results revealed that, after training, the DLD group presented greater involvement of the frontal cortex and temporal pole for EN objects. Furthermore, in the TD group, the left putamen, globus pallidus (GP) and thalamus were involved in the early stages of SL, whereas in the DLD group, these areas were involved in SL after training. For DN objects, after training, the DLD group presented greater involvement of the parietal and precuneus regions in the SL task performance. Our results suggest that children with DLD may employ different cognitive processes in SL than TD children, possibly as a compensatory mechanism.

neuroscience↗

Common but different: An ERP study of single- and multi-source interference processing in MSIT

Flexible behavior often requires processing of complex, interfering information. Research has investigated conflict-related brain processes mostly using single tasks which hindered direct comparison of different interference types. Thus, the question if they are resolved by a common mechanism or by a set of different, task-specific mechanisms remains open. In this study, we used event-related potentials (ERPs) to examine the spatio-temporal dynamics of cognitive control across Simon, flanker, multi-source and no-conflict conditions. Our findings reveal that all trial types engaged the same sequence of processing stages, as indicated by common ERP waveforms and consistent number and order of microstates across conditions. However, the intensity and duration of these common stages scaled with difficulty of the conflict task (as measured by RTs and accuracy) from Simon to flanker to multi-source interference. Flanker conflict uniquely influenced early ERP components strongly engaging the dorsal attentional system and visual areas, likely due to demands posed by the presence of flanker distractors. Later ERP components (with sources including ventral attention and somatomotor network areas) were affected by both conflicts. Accordingly, when flanker and Simon conflicts were presented together, early processes lineary summed up, but there was an interaction at the later stage of processing paralleling nonlinear drop of accuracy in a multi-conflict condition. Our study provides novel insights into the neural dynamics underlying cognitive control engaged across different conflict types and their interaction. The use of source analysis allowed us to ground ERP-based findings in the wider context of studies, including those using neuroimaging techniques. Highlights- The same processing stages, in same order are evoked in control and conflict trials - Their intensity/duration scale with conflict behavioral difficulty - Flanker conflict demands enhanced early attentional (DAN) and visual processing - Flanker and Simon interact at the late-stage processing involving VAN and SM networks - Flanker and Simon interaction is sublinear

neuroscience↗

Cortical thinning in temporal pole, a core region in Alzheimer's disease, in non-demented, middle-aged APOE-e4 and PICALM-AA/AG carriers

The symptoms of Alzheimers disease (AD) are caused by neurodegeneration and atrophy in particular brain regions, especially in the temporal cortex. However, the influence of genetic risk on cortical thickness in non-demented individuals prior to disease onset remains unclear. This study aimed to explore the relationship between two AD risk genes (APOE/PICALM) and cortical thickness in selected regions of interest (ROIs) in non-demented, middle-aged individuals. Sixty-nine (N = 69) participants (34 females, 35 males; age: 55.45{+/-}3.19) underwent magnetic resonance imaging (MRI). They were divided into three groups based on their AD risk. Cortical thickness was analyzed using CAT12 software (surface-based morphometry with the Destrieux atlas) based on T1-weighted MR images in five ROIs referred as "the cortical signature of AD" in previous studies. APOE-{varepsilon}4 with PICALM-AA/AG carriers (A+P-) are characterized by a thinner cortex in the right temporal pole compared to non-carriers, controlling for sex. No other differences in cortical thickness were found in the selected ROIs. The direction of the findings aligns with existing literature reporting cortical thinning in amyloid-positive individuals, as well as in patients with mild cognitive impairment and Alzheimers disease when compared to control groups.

neuroscience↗

Alzheimer's disease-like features in resting state EEG/fMRI of cognitively intact and healthy middle-aged APOE/PICALM risk carriers

IntroductionGenetic susceptibility is a primary factor contributing to etiology of late-onset Alzheimers disease (LOAD). The exact mechanisms and timeline through which APOE/PICALM influence brain functions and contribute to LOAD remain unidentified. This includes their effects on individuals prior to the development of the disease. MethodsAPOE/PICALM alleles were assessed to determine the genetic risk of LOAD in 79 healthy, middle-aged participants who underwent EEG and fMRI recordings. The resting-state signal was analyzed to estimate relative spectral power, complexity (Higuchis algorithm), and connectivity (coherence in EEG and ICA-based connectivity in fMRI). ResultsThe main findings indicated that individuals at risk for LOAD exhibited reduced signal complexity and the so-called "slowing of EEG" which are well-known EEG markers of AD. Additionally, these individuals showed altered functional connectivity in fMRI (within attention related areas). DiscussionRisk alleles of APOE/PICALM may affect brain integrity and function prior to the onset of the disease

neuroscience↗

Common and distinct BOLD correlates of Simon and flanker conflicts which can(not) be reduced to time-on-task effects

The ability to identify and resolve conflicts between standard, well trained behaviors, and behaviors required by the current context is an essential feature of cognitive control. To date, no consensus has been reached on the brain mechanisms involved in exerting such control: while some studies identified diverse patterns of activity across different conflicts, other studies reported common resources across conflict tasks or even across simple tasks devoid of conflict component. The latter reports attributed the entire activity observed in the presence of conflict to longer time spent on the task (i.e. to the so-called time-on-task effects). Here we used an extended Multi-Source Interference Task (MSIT) which combines Simon and flanker types of interference to determine shared and conflict-specific mechanisms of conflict resolution in fMRI, and their separability from the time-on-task effects. Large portions of the activity in the dorsal attention network and decreases of activity in the default mode network were shared across the tasks and scaled in parallel with increasing reaction times. Importantly, activity in the sensory and sensorimotor cortices, as well as in the posterior medial frontal cortex (pMFC)-a key region implicated in conflict processing-could not be exhaustively explained by the time-on-task effects.

neuroscience↗

A Spatiotemporal Reconstruction of the C. elegans Pharyngeal Cuticle Reveals a Structure Rich in Phase-Separating Proteins

Roughly 4.5 million species of ecdysozoan animals repeatedly shed their old cuticle and construct a new one underneath to accommodate growth. How cuticles are constructed is not well understood. Here, we systematically mine gene expression datasets to uncover the spatiotemporal blueprint for how the chitin-based pharyngeal cuticle of the nematode Caenorhabditis elegans is built. We demonstrate that the blueprint correctly predicts expression patterns and functional relevance to cuticle development. We find that as larvae prepare to molt, catabolic enzymes are upregulated and the genes that encode chitin synthase, chitin cross-linkers, and homologs of amyloid regulators subsequently peak in expression. 48% of the gene products secreted during the molt are predicted to be intrinsically disordered proteins (IDPs), many of which belong to four distinct families that are expressed in overlapping waves. These include the IDPAs, IDPBs, and IDPCs that are introduced for the first time here. We find that all four families have sequence properties known to drive phase separation and show in vitro phase separation for one of these proteins. This systematic analysis reveals the massive contribution that IDPs make to the cuticle and highlights how reversibly phase-separating materials may facilitate cuticle disassembly and reassembly during the molt.

systems biology↗