Evidence map›Paper›PMID 38519465›Full record

ArticleTranslational psychiatry2024

Interactions between neurotrophins, mood, and physical activity under the conditions of sleep deprivation.

Marcin Sochal, Marta Ditmer, Agata Binienda, Aleksandra Tarasiuk, Piotr Białasiewicz, Szymon Turkiewicz, Filip Franciszek Karuga, Fichna Jakub, Agata Gabryelska

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Exploring Dapagliflozin's Influence on Autophagic Flux in Mania-like Behaviour: Insights from the LKB1/AMPK/LC3 Pathway in a Mouse Model.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
    Article
  6. Review
  7. Review
  8. Glaucomatous retinal ganglion cells: death and protection.International journal of ophthalmology · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Marcin SochalDepartment of Sleep Medicine and Metabolic Disorders, Medical University of Lodz, Lodz, Poland. sochalmar@gmail.com.ORCID 0000-0003-2122-0304
Marta DitmerDepartment of Sleep Medicine and Metabolic Disorders, Medical University of Lodz, Lodz, Poland.
Agata BiniendaDepartment of Biochemistry, Medical University of Lodz, Lodz, Poland.
Aleksandra TarasiukDepartment of Biochemistry, Medical University of Lodz, Lodz, Poland.
Piotr BiałasiewiczDepartment of Sleep Medicine and Metabolic Disorders, Medical University of Lodz, Lodz, Poland.
Szymon TurkiewiczDepartment of Sleep Medicine and Metabolic Disorders, Medical University of Lodz, Lodz, Poland.
Filip Franciszek KarugaDepartment of Sleep Medicine and Metabolic Disorders, Medical University of Lodz, Lodz, Poland.
Fichna JakubDepartment of Biochemistry, Medical University of Lodz, Lodz, Poland.
Agata GabryelskaDepartment of Sleep Medicine and Metabolic Disorders, Medical University of Lodz, Lodz, Poland.
Medical University of Lodz · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sleep deprivation (DS) is the forced elimination of sleep. While brain-derived neurotrophic factor (BDNF) has been extensively studied in the context of in mood changes following DS, the role of other neurotrophins remains elusive. This study explores the impact of DS on BDNF, glial cell line-derived neurotrophic factor (GDNF), neurotrophin-3 (NT3), and neurotrophin-4 (NT4) at mRNA and protein level, considering their potential links to mood disturbances. The study involved 81 participants subjected to polysomnography (PSG) and DS. Blood samples, mood assessments, and actigraphy data were collected twice, after PSG and DS. NT mRNA expression and serum protein concentrations of BDNF, GDNF, NT3, and NT4 were measured. Participants were divided into Responders and Non-Responders based on mood improvement after DS. DS reduced BDNF mRNA expression in all participants, with no change in serum BDNF protein. GDNF protein decreased in Non-Responders, while Responders exhibited reduced GDNF mRNA. NT3 protein increased in both groups, while NT3 mRNA decreased in Respondents. NT4 protein rose universally post-DS, but NT4 mRNA remained unchanged. Physical activity (PA) negatively correlated with mRNA expression of BDNF, GDNF, and NT3 post-DS. The study's short DS duration and exclusion of immature NT forms limit comprehensive insights. GDNF, together with NT3, might play an important role in mood response to DS. PA during DS seems to impair the mRNA expression of NTs in leukocytes. Future studies on the subject of sleep deprivation might consider investigating the relationship between BDNF and NT4 in the context of their apparent redundancy.

Indexed as

Brain-Derived Neurotrophic FactorGlial Cell Line-Derived Neurotrophic FactorExerciseHumansRNA, MessengerSleep DeprivationBrain-Derived Neurotrophic FactorGlial Cell Line-Derived Neurotrophic FactorRNA, Messenger

Identifiers

PMID38519465
PMCPMC10960007
OpenAlexW4393074856

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.