Evidence map›Paper›PMID 26462180›Full record

ArticleOncotarget2015

Viscoelastic and ultrastructural characteristics of whole blood and plasma in Alzheimer-type dementia, and the possible role of bacterial lipopolysaccharides (LPS).

Janette Bester, Prashilla Soma, Douglas B Kell, Etheresia Pretorius

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
8.1field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Exploring theResearch and practice in thrombosis and haemostasis · 2024
    Article
  10. Review
  11. Article
  12. Article
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  14. TEGJournal of clinical medicine · 2021
    Review
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  17. Review
  18. Review
  19. Article
  20. Gingipain R1 and Lipopolysaccharide FromFrontiers in immunology · 2020
    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

4 authors at 2 institutions in 2 countries.

Janette BesterDepartment of Physiology, Faculty of Health Sciences, University of Pretoria, Arcadia, South Africa.
Prashilla SomaDepartment of Physiology, Faculty of Health Sciences, University of Pretoria, Arcadia, South Africa.
Douglas B KellSchool of Chemistry and The Manchester Institute of Biotechnology, The University of Manchester, Manchester, UK.
Etheresia PretoriusDepartment of Physiology, Faculty of Health Sciences, University of Pretoria, Arcadia, South Africa.
University of Pretoria · ZAUniversity of Manchester · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M017702/1FDA HHS BB/L025752/1FDA HHS BB/M017702/1
6 · The paper itself

Abstract

Alzheimer-type dementia (AD) is a neurodegenerative disorder and the most common form of dementia. Patients typically present with neuro- and systemic inflammation and iron dysregulation, associated with oxidative damage that reflects in hypercoagulability. Hypercoagulability is closely associated with increased fibrinogen and in AD patients fibrinogen has been implicated in the development of neuroinflammation and memory deficits. There is still no clear reason precisely why (a) this hypercoagulable state, (b) iron dysregulation and (c) increased fibrinogen could together lead to the loss of neuronal structure and cognitive function. Here we suggest an alternative hypothesis based on previous ultrastructural evidence of the presence of a (dormant) blood microbiome in AD. Furthermore, we argue that bacterial cell wall components, such as the endotoxin lipopolysaccharide (LPS) of Gram-negative strains, might be the cause of the continuing and low-grade inflammation, characteristic of AD. Here, we follow an integrated approach, by studying the viscoelastic and ultrastructural properties of AD plasma and whole blood by using scanning electron microscopy, Thromboelastography (TEG®) and the Global Thrombosis Test (GTT®). Ultrastructural analysis confirmed the presence and close proximity of microbes to erythrocytes. TEG® analysis showed a hypercoagulable state in AD. TEG® results where LPS was added to naive blood showed the same trends as were found with the AD patients, while the GTT® results (where only platelet activity is measured), were not affected by the added LPS, suggesting that LPS does not directly impact platelet function. Our findings reinforce the importance of further investigating the role of LPS in AD.

Indexed as

Alzheimer DiseaseHumansIronLipopolysaccharidesMicroscopy, Electron, ScanningThrombelastographyViscoelastic SubstancesIronLipopolysaccharidesViscoelastic SubstancesAlzheimer-type dementiaGerotargetiron levelslipopolysaccharidesscanning electron microscopythromboelastography

Identifiers

PMID26462180
PMCPMC4742105
OpenAlexW2191423032

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.