Evidence map›Paper›PMID 34356626›Full record

ReviewBiomolecules2021

Cognitive Impairment and Dementia: Gaining Insight through Circadian Clock Gene Pathways.

Kenneth Maiese

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
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  17. Article
  18. Article
  19. Cognitive Impairment in Multiple Sclerosis.Bioengineering (Basel, Switzerland) · 2023
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Kenneth MaieseCellular and Molecular Signaling, New York, NY 10022, USA.
Cellular Research (United States) · US

Funding

NIH HHS NS053956
6 · The paper itself

Abstract

Neurodegenerative disorders affect fifteen percent of the world's population and pose a significant financial burden to all nations. Cognitive impairment is the seventh leading cause of death throughout the globe. Given the enormous challenges to treat cognitive disorders, such as Alzheimer's disease, and the inability to markedly limit disease progression, circadian clock gene pathways offer an exciting strategy to address cognitive loss. Alterations in circadian clock genes can result in age-related motor deficits, affect treatment regimens with neurodegenerative disorders, and lead to the onset and progression of dementia. Interestingly, circadian pathways hold an intricate relationship with autophagy, the mechanistic target of rapamycin (mTOR), the silent mating type information regulation 2 homolog 1

Indexed as

Circadian ClocksGene Expression RegulationAlzheimer DiseaseAnimalsCognitive DysfunctionForkhead Transcription FactorsHumansSirtuin 1TOR Serine-Threonine KinasesForkhead Transcription FactorsMTOR protein, humanSIRT1 protein, humanSirtuin 1TOR Serine-Threonine KinasesAlzheimer’s diseaseautophagycircadian rhythmdementiaerythropoietinforkheadFoxOglymphatic pathwaymechanistic target of rapamycin (mTOR)Parkinson’s diseasesilent mating type information regulation 2 homolog 1sleep fragmentation

Identifiers

PMID34356626
PMCPMC8301848
OpenAlexW3181603524

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.