bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.09.30.679650

The relationship between sleep, mental health, and performance on tests of pattern separation in young adults

Abstract

ObjectivesYoung adults experience the highest rates of mental health disorders of any age group. Given that mental health disorders are associated with sleep disturbances and cognitive impairments, we investigated whether sleep moderates the effects on cognition. MethodsUniversity students (N=89; aged 18-30 years) remotely monitored their sleep for seven consecutive days using wrist actigraphy and sleep diaries. On day seven, participants completed cognitive testing and mental health questionnaires. Cognitive tests included the Psychomotor Vigilance Task (PVT), Cambridge Neuropsychological Test Automated Battery (CANTAB), and the Mnemonic Similarity Task (MST). CANTABs Delayed Matching to Sample (DMS) and MST are designed to tax pattern separation, a computational mechanism supporting encoding of similar experiences as distinct representations. Becks Depression Inventory and Becks Anxiety Inventory assessed mental health. ResultsEighty participants (mean age: 20.13{+/-}2.00) were included in the analyses. Most participants reported mild to severe depressive and anxiety symptoms. Depressive symptoms were correlated with wake-up time ({rho}=.35, p=.002) as well as PVT ({rho}=.26, p=.02) and DMS ({rho}=.24, p=.04) performance. Bedtime was correlated with performance on MST (r=-.29, r=.02) and DMS ({rho}=.25, p=.03), while wake-up time was correlated with performance on MST (r=- .31, p=.01) and DMS ({rho}=.28, p=.01). Sleep did not moderate the effects of mental health on cognitive performance. ConclusionCognitive tests taxing pattern separation are sensitive to depressive symptoms and sleep timing. While students face a disproportionate burden of mental health disorders compromising cognitive functioning, improving sleep quality may offer a partial, though not moderating, pathway to alleviating these cognitive impairments.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Roenningen, A. E., Gill, D., Kent, B. A.. 2025-10-02. The relationship between sleep, mental health, and performance on tests of pattern separation in young adults. https://doi.org/10.1101/2025.09.30.679650

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

The Unreasonable Effectiveness of Cell Types in Describing Neuronal Physiological Features

Single-cell RNA sequencing (scRNA-seq) captures detailed gene expression profiles at scale, while patch-clamp recordings measure intrinsic neuronal electrophysiological properties. Modeling the relations between these two modalities remains a challenge. Here, we compare how well electrophysiological features can be predicted by traditional transcriptomic cell type classification, representations derived from a foundational model (scGPT) pretrained on large-scale scRNA-seq datasets, ion channel-coding genes, and highly variable genes. Using paired transcriptomic and electrophysiological patch-sequencing data from 495 human neurons from neurosurgical tissue, we find that cluster-level cell type representations consistently outperform highly variable gene selection, ion channel gene selection, and context-enriched scGPT embeddings. Notably, performance varies across model architectures and initializations, and the best results are obtained by combining the outputs of separate cell type and scGPT-based models. Together, these findings suggest that traditional discrete cellular classification is highly effective in predicting physiological features. For maximum performance it can be complemented by pretrained transformer models.

neuroscience↗

A nonlinear inhibition pathway underlying cortical responses to tuned holographic optogenetic perturbations

Optogenetics enables causal manipulation of cortical activity. Perturbation responses can be counterintuitive due to network interactions, making theory essential for predicting them. Existing approaches often rely on linear approximations, which fail for many biologically relevant perturbations. Here we develop a nonlinear theory of responses to holographic perturbations in cell-type-specific recurrent networks with structured connectivity. We fit a nonlinear model to mouse V1 data, which shows cotuned-ensemble suppression: perturbing spatially clustered neurons with similar preferred orientations yields markedly stronger short-range suppression than perturbing untuned ensembles. We show that cotuned-ensemble suppression arises from a feature-tuned, nonlinear inhibition pathway implicating somatostatin-positive (SST) interneurons. The theory predicts that cotuned ensembles suppress parvalbumin-positive (PV) neurons but facilitate SST neurons, and links the degree of cotuned-ensemble suppression or facilitation to the variance of the SST response. This framework identifies mechanisms by which nonlinear inhibition sculpts cortical dynamics and establishes a predictive basis for targeted optogenetic interventions.

neuroscience↗

Proteomic signatures of APOE ε4 across human tissues and cell types in Alzheimers disease

The apolipoprotein E {varepsilon}4 (APOE {varepsilon}4) allele is the strongest genetic risk factor for late-onset Alzheimers disease (AD). However, the underlying molecular mechanisms remain unclear. This study included 1691 participants from the Religious Orders Study and Rush Memory and Aging Project (ROSMAP), 1226 participants from the Accelerating Medicines Partnership - Alzheimers Disease (AMP-AD) Diverse Cohorts Study, and 735 participants from the Alzheimers Disease Neuroimaging Initiative (ADNI). To characterise APOE {varepsilon}4 molecular effects, we analysed proteomic data from plasma, cerebrospinal fluid (CSF), and induced pluripotent stem cell (iPSC)-derived astrocytes and neurons, as well as transcriptomic and proteomic data from multiple brain regions. The association of APOE {varepsilon}4 with AD neuropathology was also examined. APOE {varepsilon}4 carriers shared a plasma proteomic signature enriched for immune processes, irrespective of AD diagnosis. A machine learning classifier trained on this signature discriminated APOE {varepsilon}4 carriers from non-carriers in an independent cohort using CSF proteomics. APOE {varepsilon}4 carriage was associated with higher Braak stages and Consortium to Establish a Registry for Alzheimers Disease (CERAD) score. However, only limited APOE {varepsilon}4-associated transcriptomic and proteomic changes were observed in bulk brain tissue, with poor cross-layer concordance. Proteomic analyses of iPSC-derived astrocytes and neurons further revealed cell-type-specific APOE {varepsilon}4-associated changes. APOE {varepsilon}4 is associated with a consistent proteomic signature across plasma and CSF. Its molecular effects in the brain differ across cell types, brain regions and molecular layers. These findings support the need for cell-type-resolved multi-omic studies to elucidate how APOE {varepsilon}4 confers AD risk.

neuroscience↗