Publications by authors named "Annette Milnik"

Background: Early mobilisation (EM) is an intervention that may improve the outcome of critically ill patients. There is limited data on EM in COVID-19 patients and its use during the first pandemic wave.

Methods: This is a pre-planned subanalysis of the ESICM UNITE-COVID, an international multicenter observational study involving critically ill COVID-19 patients in the ICU between February 15th and May 15th, 2020.

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Previous studies have shown that females typically outperform males on episodic memory tasks. In this study, we investigated if (1) there are differences between males and females in their connectome characteristics, (2) if these connectivity patterns are associated with memory performance, and (3) if these brain connectome characteristics contribute to the differences in episodic memory performance between sexes. In a sample of 655 healthy young subjects (n = 391 females; n = 264 males), we derived brain network characteristics from diffusion-weighted imaging (DWI) data using models of crossing fibers within each voxel of the brain and probabilistic tractography (graph strength, shortest path length, global efficiency, and weighted transitivity).

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Background: Corona Virus Disease 2019 (COVID-19) patients display risk factors for intensive care unit acquired weakness (ICUAW). The pandemic increased existing barriers to mobilisation. This study aimed to compare mobilisation practices in COVID-19 and non-COVID-19 patients.

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Article Synopsis
  • This study looked at how safe and possible it is to move seriously ill patients in a hospital when they are given a medicine called norepinephrine.
  • Researchers checked the records of over 12,000 patients from 16 different ICUs in Germany to see how often and when they were able to mobilise or move around.
  • The results showed that higher doses of norepinephrine made it less likely for patients to move out of bed, but it didn't seem to affect how many patients survived or cause more problems.
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Emotional information is better remembered than neutral information. Extensive evidence indicates that the amygdala and its interactions with other cerebral regions play an important role in the memory-enhancing effect of emotional arousal. While the cerebellum has been found to be involved in fear conditioning, its role in emotional enhancement of episodic memory is less clear.

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Only a small proportion of what we see can later be recalled. Up to date it is unknown how far differences in visual exploration during encoding affect the strength of episodic memories. Here, we identified individual gaze characteristics by analyzing eye tracking data in a picture encoding task performed by 967 healthy subjects during fMRI.

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Background: Recognition memory is an essential ability for functioning in everyday life. Establishing robust brain networks linked to recognition memory performance can help to understand the neural basis of recognition memory itself and the interindividual differences in recognition memory performance.

Methods: We analysed behavioural and whole-brain fMRI data from 1'410 healthy young adults during the testing phase of a picture-recognition task.

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The amygdala is critically involved in emotional processing, including fear responses, and shows hyperactivity in anxiety disorders. Previous research in healthy participants has indicated that amygdala activity is down-regulated by cognitively demanding tasks that engage the PFC. It is unknown, however, if such an acute down-regulation of amygdala activity might correlate with reduced fear in anxious participants.

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  • Emotional perception and memory can change throughout the menstrual cycle, but the effects of hormonal contraceptives (HC) on these aspects are less understood.
  • In a study of 2,169 healthy young women, HC users rated emotional images as more impactful and recalled them better than those not using HC.
  • The connection between HC use and improved memory was partly influenced by how HC users perceived the emotions of the pictures, suggesting a link that could lead to more research on emotional memory and anxiety disorders in women.
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  • Our brains have different areas that help us remember and feel emotions, like happiness or sadness, and these areas work together.
  • Researchers studied healthy young adults to see how their brains reacted when looking at pictures that made them feel different emotions and when they tried to remember those pictures later.
  • They found specific patterns in brain activity that could predict how strongly someone felt emotions and how well they remembered the pictures, which can help in understanding emotional problems in mental health.
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  • PTSD risk is influenced by previous traumatic experiences and genetic factors, with a focus on a specific SNP (rs3852144) associated with resilience against PTSD development.
  • A genome-wide association study identified seven significant SNPs linked to lifetime PTSD risk among war survivors, with one SNP being replicated in a different group of genocide survivors.
  • The presence of the minor G-allele of rs3852144 appears to reduce PTSD vulnerability and emotional memory formation, though its effects on therapy outcomes remain unclear and require further investigation.
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The risk of developing posttraumatic stress disorder (PTSD) increases with the number of traumatic event types experienced (trauma load) in interaction with other psychobiological risk factors. The NOTCH (neurogenic locus notch homolog proteins) signaling pathway, consisting of four different trans-membrane receptor proteins (NOTCH1-4), constitutes an evolutionarily well-conserved intercellular communication pathway (involved, e.g.

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Working memory (WM) is an important cognitive domain for everyday life functioning and is often disturbed in neuropsychiatric disorders. Functional magnetic resonance imaging (fMRI) studies in humans show that distributed brain areas typically described as fronto-parietal regions are implicated in WM tasks. Based on data from a large sample of healthy young adults ( = 1369), we applied independent component analysis (ICA) to the WM-fMRI signal and identified two distinct networks that were relevant for differences in individual WM task performance.

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The large biological distance between genetic risk loci and their mechanistic consequences in the tissue of interest limits the ability to establish functionality of susceptibility variants for genetically complex traits. Such a biological gap may be reduced through the systematic study of molecular mediators of genomic action, such as epigenetic modification. Here, we report the identification of robust genetic estimators of whole-blood CpG methylation, which can serve as intermediate molecular traits amenable to association testing with other genetically complex traits.

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  • The study looked at how looking at emotional pictures affects the brain later on, especially how different brain areas connect with each other.
  • Researchers used an MRI scan to see if showing scary or sad pictures changes the way the brain works compared to neutral pictures in 34 healthy young adults.
  • They found that even though the scary pictures made people feel strong emotions, it didn’t change how different parts of the brain were connected when people were resting afterwards.
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Studies assessing the existence and magnitude of epistatic effects on complex human traits provide inconclusive results. The study of such effects is complicated by considerable increase in computational burden, model complexity, and model uncertainty, which in concert decrease model stability. An additional source introducing significant uncertainty with regard to the detection of robust epistasis is the biological distance between the genetic variation and the trait under study.

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Introduction: Memory functions are highly variable between healthy humans. The neural correlates of this variability remain largely unknown.

Methods: Here, we investigated how differences in free recall performance are associated with DTI-based properties of the brain's structural connectome and with grey matter volumes in 664 healthy young individuals tested in the same MR scanner.

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The identification of genes related to encoding, storage, and retrieval of memories is a major interest in neuroscience. In the current study, we analyzed the temporal gene expression changes in a neuronal mRNA pool during an olfactory long-term associative memory (LTAM) in hermaphrodites. Here, we identified a core set of 712 (538 upregulated and 174 downregulated) genes that follows three distinct temporal peaks demonstrating multiple gene regulation waves in LTAM.

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  • Increasing age is linked to a decrease in neocortex thickness, with unknown biological mechanisms involved.
  • An identified epigenetic signature is associated with cortical thickness and memory performance in healthy young adults, and this effect was replicated in individuals with major depressive disorder.
  • The study's findings suggest that specific genes related to the immune system might play a role, and analyzing blood methylation patterns could enhance our understanding of brain-related traits.
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Depressive symptoms exist on a continuum, the far end of which is found in depressive disorders. Utilizing the continuous spectrum of depressive symptoms may therefore contribute to the understanding of the biological underpinnings of depression. Gene set enrichment analysis (GSEA) is an important tool for the identification of gene groups linked to complex traits, and was applied in the present study on genome-wide association study (GWAS) data of depression scores and their brain-level structural correlates in healthy young individuals.

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DNA methylation represents an important link between structural genetic variation and complex phenotypes. The study of genome-wide CpG methylation and its relation to traits relevant to psychiatry has become increasingly important. Here, we analyzed quality metrics of 394,043 CpG sites in two samples of 568 and 319 mentally healthy young adults.

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Importance: Human episodic memory performance is linked to the function of specific brain regions, including the hippocampus; declines as a result of increasing age; and is markedly disturbed in Alzheimer disease (AD), an age-associated neurodegenerative disorder that primarily affects the hippocampus. Exploring the molecular underpinnings of human episodic memory is key to the understanding of hippocampus-dependent cognitive physiology and pathophysiology.

Objective: To determine whether biologically defined groups of genes are enriched in episodic memory performance across age, memory encoding-related brain activity, and AD.

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Episodic memory performance is the result of distinct mental processes, such as learning, memory maintenance, and emotional modulation of memory strength. Such processes can be effectively dissociated using computational models. Here we performed gene set enrichment analyses of model parameters estimated from the episodic memory performance of 1,765 healthy young adults.

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The dorsolateral prefrontal cortex (DLPFC) plays a key role in working memory. Evidence indicates that transcranial magnetic stimulation (TMS) over the DLPFC can interfere with working memory performance. Here we investigated for how long continuous theta-burst stimulation (cTBS) over the DLPFC decreases working memory performance and whether the effect of cTBS on performance depends on working memory load.

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