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Wolak, T.

Publications and source records attributed to Wolak, T..

8 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↗

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↗

Resting-state functional connectivity changes following audio-tactile speech training

Understanding speech in background noise is a challenging task, especially if the signal is also distorted. In a series of previous studies we have shown that comprehension can improve if simultaneously to the auditory speech, the person receives speech-extracted low-frequency signals on fingertips. The effect increases after short audio-tactile speech training. Here we use resting-state functional magnetic resonance, measuring spontaneous low-frequency oscillations in the brain while at rest, to assess training-induced changes in functional connectivity. We show enhanced connectivity within a right-hemisphere cluster encompassing the middle temporal motion area (MT), and the extrastriate body area (EBA), and lateral occipital cortex (LOC), which before training is found to be more connected to bilateral dorsal anterior insula. Furthermore, early visual areas are found to switch from increased connectivity with the auditory cortex before, to increased connectivity with an association sensory/multisensory parietal hub, contralateral to the palm receiving vibrotactile inputs, after. Also the right sensorimotor cortex, including finger representations, is more connected internally after training. The results alltogether can be interpreted within two main complementary frameworks. One, speech-specific, relates to the pre-existing brain connectivity for audio-visual speech processing, including early visual, motion and body regions for lip-reading and gesture analysis in difficult acoustic conditions, which the new audio-tactile speech network might be built upon. The other refers to spatial/body awareness and audio-tactile integration, including in the revealed parietal and insular regions. It is possible that an extended training period may be necessary to more effectively strengthen direct connections between the auditory and sensorimotor brain regions, for the utterly novel speech comprehension task. The outcomes of the study can be relevant for both basic neuroscience, as well as development of rehabilitation tools for the hearing impaired population.

neuroscience↗

Neuronal basis of audio-tactile speech perception

Since childhood, we experience speech as a combination of audio and visual signals, with visual cues particularly beneficial in difficult auditory conditions. This study investigates an alternative multisensory context of speech, and namely audio-tactile, which could prove beneficial for rehabilitation in the hearing impaired population. We show improved understanding of distorted speech in background noise, when combined with low-frequency speech-extracted vibrotactile stimulation delivered on fingertips. The quick effect might be related to the fact that both auditory and tactile signals contain the same type of information. Changes in functional connectivity due to audio-tactile speech training are primarily observed in the visual system, including early visual regions, lateral occipital cortex, middle temporal motion area, and the extrastriate body area. These effects, despite lack of visual input during the task, possibly reflect automatic involvement of areas supporting lip-reading and spatial aspects of language, such as gesture observation, in difficult acoustic conditions. For audio-tactile integration we show increased connectivity of a sensorimotor hub representing the entire body, with the parietal system of motor planning based on multisensory inputs, along with several visual areas. After training, the sensorimotor connectivity increases with high-order and language-related frontal and temporal regions. Overall, the results suggest that the new audio-tactile speech task activates regions that partially overlap with the established brain network for audio-visual speech processing. This further indicates that neuronal plasticity related to perceptual learning is first built upon an existing structural and functional blueprint for connectivity. Further effects reflect task-specific behaviour related to body and spatial perception, as well as tactile signal processing. Possibly, a longer training regime is required to strengthen direct pathways between the auditory and sensorimotor brain regions during audio-tactile speech processing.

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↗

Local variation in brain temperature explains gender-specificity of working memory performance

Exploring gender differences in cognitive abilities offers vital insights into human brain functioning. Our study utilized advanced techniques like magnetic resonance thermometry, standard working memory n-back tasks, and functional MRI to investigate if gender-based variations in brain temperature correlate with distinct neuronal responses and working memory capabilities. Interestingly, our findings revealed no gender disparity in working memory performance. However, we observed a significant decrease in average brain temperature in males during working memory tasks, a phenomenon not seen in females. Although changes in female brain temperature were not statistically significant, we found an inverse relationship between the absolute temperature change (ATC) and cognitive performance, alongside a correlation with blood oxygen level dependent (BOLD) neuronal responses. This suggests that in females, ATC is a crucial determinant for the link between cognitive performance and BOLD responses, a linkage not evident in males. Our results also suggest that females compensate for their brains heightened temperature sensitivity by activating additional neuronal networks to support working memory. This study not only underscores the complexity of gender differences in cognitive processing but also opens new avenues for understanding how temperature fluctuations influence brain functionality. SignificanceSex/gender differences in cognition are of high scientific and social interest. Yet, those differences (if any) remain elusive. Here we used magnetic resonance thermometry and functional MRI to examine, whether gender differences in working memory performance (WMP) are determined by subtle, yet detectable between-sex differences in local brain temperature fluctuations mediated by blood oxygen level-dependent (BOLD) neuronal responses. We found that WMP did not differ between genders. Yet, a females WMP was more sensitive to brain temperature variation compared to males. Furthermore, the negative impact of temperature on female cognitive functions was compensated by higher BOLD activity in other task-specific brain areas. This compensation may account for equivocal results of studies on the between-sex differences in cognitive performance.

neuroscience↗

Epigenetic liquid biopsies reveal elevated vascular endothelial cell turnover and erythropoiesis in asymptomatic COVID-19 patients

The full spectrum of tissues affected by SARS-CoV-2 infection is crucial for deciphering the heterogenous clinical course of COVID-19. Here, we analyzed DNA methylation and histone modification patterns in circulating chromatin to assess cell type-specific turnover in severe and asymptomatic COVID-19 patients, in relation to clinical outcome. Patients with severe COVID-19 had a massive elevation of circulating cell-free DNA (cfDNA) levels, which originated in lung epithelial cells, cardiomyocytes, vascular endothelial cells and erythroblasts, suggesting increased cell death or turnover in these tissues. The immune response to infection was reflected by elevated B cell and monocyte/macrophage cfDNA levels, and by evidence of an interferon response in cells prior to cfDNA release. Strikingly, monocyte/macrophage cfDNA levels (but not monocyte counts), as well as lung epithelium cfDNA and vascular endothelial cfDNA, predicted clinical deterioration and duration of hospitalization. Asymptomatic patients had elevated levels of immune-derived cfDNA but did not show evidence of pulmonary or cardiac damage. Surprisingly, these patients showed elevated levels of vascular endothelial cell and erythroblast cfDNA, suggesting that sub-clinical vascular and erythrocyte turnover are universal features of COVID-19, independent of disease severity. Epigenetic liquid biopsies provide non-invasive means of monitoring COVID-19 patients, and reveal sub-clinical vascular damage and red blood cell turnover.

microbiology↗

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↗