Evidence map›Paper›PMID 28163132›Full record

ReviewExperimental gerontology2017

Aging leads to altered microglial function that reduces brain resiliency increasing vulnerability to neurodegenerative diseases.

Paula C Bickford, Antwoine Flowers, Bethany Grimmig

Abstract readReview
In one paragraph

Review in Experimental gerontology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Age-Induced Spatial Memory Deficits in Rats Are Correlated with Specific Brain Region Alterations in Microglial Morphology and Gene Expression.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Old Maids: Aging and Its Impact on Microglia Function.International journal of molecular sciences · 2017
    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

3 authors.

Paula C BickfordResearch Service, James A. Haley Veterans Administration Hospital, 13000 Bruce B Downs Blvd, Tampa, FL, United States; Center of Excellence for Aging and Brain Repair, Dept. of Neurosurgery and Brain Repair, Morsani College of Medicine, University of South Florida, Tampa, FL, United States. Electronic address: pbickfor@health.usf.edu.
Antwoine FlowersCenter of Excellence for Aging and Brain Repair, Dept. of Neurosurgery and Brain Repair, Morsani College of Medicine, University of South Florida, Tampa, FL, United States.
Bethany GrimmigCenter of Excellence for Aging and Brain Repair, Dept. of Neurosurgery and Brain Repair, Morsani College of Medicine, University of South Florida, Tampa, FL, United States.

Funding

STATISTICAL COREP01AG004418 · NIA · UNIVERSITY OF SOUTH FLORIDA · PI SMALL, BRENT JOHN · 1985 to 2010
$11.6M
Neuron - glial communication and brain agingR01AG044919 · NIA · UNIVERSITY OF SOUTH FLORIDA · PI BICKFORD, PAULA C · 2012 to 2016
$1.7M
Regulation of microglial priming with age and the impact on neural plasticityR36AG051747 · NIA · UNIVERSITY OF SOUTH FLORIDA · PI FLOWERS, ANTWOINE · 2015 to 2016
$129k
Aging and Microglial PolarizationI01BX003421 · VA · JAMES A. HALEY VA MEDICAL CENTER · PI BICKFORD, PAULA C · 2016 to 2020
–
BLRD VA I01 BX003421NIA NIH HHS P01 AG004418NIA NIH HHS R01 AG044919NIA NIH HHS R36 AG051747
6 · The paper itself

Abstract

Aging is the primary risk factor for many neurodegenerative diseases. Thus, understanding the basic biological changes that take place with aging that lead to the brain being less resilient to disease progression of neurodegenerative diseases such as Parkinson's disease or Alzheimer's disease or insults to the brain such as stroke or traumatic brain injuries. Clearly this will not cure the disease per se, yet increasing the ability of the brain to respond to injury could improve long term outcomes. The focus of this review is examining changes in microglia with age and possible therapeutic interventions involving the use of polyphenol rich dietary supplements.

Indexed as

Cellular SenescenceNerve DegenerationAge FactorsAgingAnimalsAnti-Inflammatory AgentsBrainDietary SupplementsHumansInflammation MediatorsMicrogliaNeural Stem CellsNeurodegenerative DiseasesNeuronal PlasticityNeuroprotective AgentsPolyphenolsAnti-Inflammatory AgentsInflammation MediatorsNeuroprotective AgentsPolyphenolsMicrogliaPolyphenol

Identifiers

PMID28163132
PMCPMC5469713

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.