Evidence map›Paper›PMID 33255513›Full record

ReviewInternational journal of molecular sciences2020

Peripheral Glycolysis in Neurodegenerative Diseases.

Simon M Bell, Toby Burgess, James Lee, Daniel J Blackburn, Scott P Allen, Heather Mortiboys

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 97 citations in OpenAlex.

  1. Metabolic profiles associated with fat loss in Parkinson's disease.Journal of neurology, neurosurgery, and psychiatry · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
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  9. Interconnections of insulin/IGF-1 signaling and autophagy abnormalities in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. The regulatory roles and clinical significance of glycolysis in tumor.Cancer communications (London, England) · 2024
    Review
  18. Review
  19. Article
  20. Article
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

6 authors at 1 institution in 1 country.

Simon M BellSheffield Institute for Translational Neurosciences, University of Sheffield, Sheffield S10 2HQ, UK.ORCID 0000-0002-2781-6478
Toby BurgessSheffield Institute for Translational Neurosciences, University of Sheffield, Sheffield S10 2HQ, UK.
James LeeSheffield Institute for Translational Neurosciences, University of Sheffield, Sheffield S10 2HQ, UK.
Daniel J BlackburnSheffield Institute for Translational Neurosciences, University of Sheffield, Sheffield S10 2HQ, UK.
Scott P AllenSheffield Institute for Translational Neurosciences, University of Sheffield, Sheffield S10 2HQ, UK.ORCID 0000-0003-4418-7375
Heather MortiboysSheffield Institute for Translational Neurosciences, University of Sheffield, Sheffield S10 2HQ, UK.
University of Sheffield · GB

Funding

Alzheimer's Research UK ARUK-PCRF2016A-1Neuroscience Research Institute Foundation naNIHR Sheffield Biomedical Research Center NAParkinson's UK F-1301Parkinson's UK F1301Wellcome Trust 216340/Z/19/Z
6 · The paper itself

Abstract

Neurodegenerative diseases are a group of nervous system conditions characterised pathologically by the abnormal deposition of protein throughout the brain and spinal cord. One common pathophysiological change seen in all neurodegenerative disease is a change to the metabolic function of nervous system and peripheral cells. Glycolysis is the conversion of glucose to pyruvate or lactate which results in the generation of ATP and has been shown to be abnormal in peripheral cells in Alzheimer's disease, Parkinson's disease, and Amyotrophic Lateral Sclerosis. Changes to the glycolytic pathway are seen early in neurodegenerative disease and highlight how in multiple neurodegenerative conditions pathology is not always confined to the nervous system. In this paper, we review the abnormalities described in glycolysis in the three most common neurodegenerative diseases. We show that in all three diseases glycolytic changes are seen in fibroblasts, and red blood cells, and that liver, kidney, muscle and white blood cells have abnormal glycolysis in certain diseases. We highlight there is potential for peripheral glycolysis to be developed into multiple types of disease biomarker, but large-scale bio sampling and deciphering how glycolysis is inherently altered in neurodegenerative disease in multiple patients' needs to be accomplished first to meet this aim.

Indexed as

Adenosine TriphosphateAlzheimer DiseaseAmyotrophic Lateral SclerosisBrainGlucoseGlycolysisHumansNeurodegenerative DiseasesParkinson DiseaseSpinal CordAdenosine TriphosphateGlucoseAlzheimer’s diseasefibroblastsglycolysismotor neuron diseasemuscleParkinson’s diseasered blood cells

Identifiers

PMID33255513
PMCPMC7727792
OpenAlexW3109588679

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.