# Associations Between Sleep Deprivation, Circadian Gene Expression, Depressive Symptoms, and Psychomotor Performance—Preliminary Results

**Authors:** Marta Ditmer, Agata Gabryelska, Aleksandra Wojtera, Aleksandra Tarasiuk-Zawadzka, Agata Binienda, Szymon Turkiewicz, Filip Franciszek Karuga, Piotr Białasiewicz, Jakub Fichna, Dominik Strzelecki, Marcin Sochal

PMC · DOI: 10.3390/jcm15041331 · Journal of Clinical Medicine · 2026-02-08

## TL;DR

This study explores how sleep deprivation affects mood and coordination, and how circadian genes might explain these effects.

## Contribution

The study links specific circadian gene expression patterns to individual differences in psychomotor performance after sleep deprivation.

## Key findings

- In non-responders, higher BMAL1, CRY1, PER1, and NR1D1 expression correlated with more coordination errors after sleep deprivation.
- PER1 gene expression explained 57.8% of the variability in coordination errors among non-responders.

## Abstract

Background: Deprivation of sleep (DS) might affect mood and cognitive abilities, including psychomotor functions (PF). Molecular mechanisms underlying these effects remain unclear, though studies suggest that the circadian rhythm plays a role. Methods: Seventy participants underwent polysomnography (PSG) and DS. PF was evaluated using Bimanual Eye–Hand Coordination Test (BEHCT). Mood, PF, and clock gene expression (Circadian Locomotor Output Cycles Kaput (CLOCK), Brain and Muscle ARNT-Like 1 (BMAL1), Period Circadian Regulator 1 (PER1), Cryptochrome Circadian Regulator 1 (CRY1), Nuclear Receptor Subfamily 1 Group D Member 1 (NR1D1), and Neuronal PAS Domain Protein 2 (NPAS2)) were analyzed post-PSG and post-DS. Mood changes after DS classified participants as responders (RE) or non-responders (NR). Results: In NRs, but not REs, the BEHCT error count positively correlated with the expression of BMAL1, CRY1, PER1, NR1D1 (R = 0.60, p = 0.002; R = 0.49, p = 0.018; R = 0.57, p = 0.023; and R = 0.53, p = 0.011, respectively), with PER1 explaining its variability in 57.8% (b = 0.174, R2 = 0.578, F = 20.144, and p < 0.001). Conclusions: Obtained results suggest that altered clock gene expression may contribute to individual differences in mood and PF following DS.

## Linked entities

- **Genes:** CLOCK (clock circadian regulator) [NCBI Gene 9575], BMAL1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 406], PER1 (period circadian regulator 1) [NCBI Gene 5187], CRY1 (cryptochrome circadian regulator 1) [NCBI Gene 1407], NR1D1 (nuclear receptor subfamily 1 group D member 1) [NCBI Gene 9572], NPAS2 (neuronal PAS domain protein 2) [NCBI Gene 4862]

## Full-text entities

- **Genes:** PER3 (period circadian regulator 3) [NCBI Gene 8863] {aka FASPS3, GIG13}, BMAL1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 406] {aka ARNTL, ARNTL1, BMAL1c, JAP3, MOP3, PASD3}, NT3 [NCBI Gene 4877], NR1D1 (nuclear receptor subfamily 1 group D member 1) [NCBI Gene 9572] {aka EAR1, REVERBA, REVERBalpha, THRA1, THRAL, ear-1}, Gdnf (glial cell line derived neurotrophic factor) [NCBI Gene 14573] {aka ATF}, CLOCK (clock circadian regulator) [NCBI Gene 9575] {aka KAT13D, bHLHe8}, NTF3 (neurotrophin 3) [NCBI Gene 4908] {aka HDNF, NGF-2, NGF2, NT-3, NT3}, PER2 (period circadian regulator 2) [NCBI Gene 8864] {aka FASPS, FASPS1}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, Ntf5 (neurotrophin 5) [NCBI Gene 78405] {aka 2900040K06Rik, NT-4, NT-5, NT4, NT4/5, Ntf-5}, NTF4 (neurotrophin 4) [NCBI Gene 4909] {aka GLC10, GLC1O, NT-4, NT-4/5, NT-5, NT4}, GAPDH (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 2597] {aka G3PD, GAPD, HEL-S-162eP}, NPAS2 (neuronal PAS domain protein 2) [NCBI Gene 4862] {aka MOP4, PASD4, bHLHe9}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], PER1 (period circadian regulator 1) [NCBI Gene 5187] {aka PER, RIGUI, hPER}, GDNF (glial cell derived neurotrophic factor) [NCBI Gene 2668] {aka ATF, ATF1, ATF2, HFB1-GDNF, HSCR3}, CRY1 (cryptochrome circadian regulator 1) [NCBI Gene 1407] {aka DSPD, PHLL1}, NGFR (nerve growth factor receptor) [NCBI Gene 4804] {aka CD271, Gp80-LNGFR, TNFRSF16, p75(NTR), p75NTR}
- **Diseases:** PF (MESH:D011596), Parkinson's disease (MESH:D010300), sleep disorders (MESH:D012893), injury to (MESH:D014947), sleep disruption (MESH:D019958), malignancies (MESH:D009369), infection (MESH:D007239), substance dependence (MESH:D019966), fatigue (MESH:D005221), Depression (MESH:D003866), Mood (MESH:D019964), DS (MESH:D012892), chronic diseases (MESH:D002908), basal cell carcinoma (MESH:D002280), Metabolic Disorders (MESH:D008659)
- **Chemicals:** oxygen (MESH:D010100), melatonin (MESH:D008550), DS (-), cortisol (MESH:D006854), TRIzol (MESH:C411644)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12940950/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940950/full.md

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Source: https://tomesphere.com/paper/PMC12940950