Evidence map›Paper›PMID 28766905›Full record

ArticleAging cell2017

Evidence for reduced neurogenesis in the aging human hippocampus despite stable stem cell markers.

Kathryn J Mathews, Katherine M Allen, Danny Boerrigter, Helen Ball, Cynthia Shannon Weickert, Kay L Double

Abstract read
In one paragraph

Article in Aging cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing 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

78 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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  5. Article
  6. Boosting Neurogenesis as a Strategy in Treating Alzheimer's Disease.International journal of molecular sciences · 2025
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
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  16. Review
  17. Article
  18. Antioxidants (Basel, Switzerland) · 2024
    Article
  19. Review
  20. Review

18 more citing papers are in PubMed but not listed here.

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.

Kathryn J MathewsDiscipline of Biomedical Science and Brain and Mind Centre, Sydney Medical School, The University of Sydney, Sydney, NSW, 2006, Australia.
Katherine M AllenNeuroscience Research Australia, Randwick, NSW, 2031, Australia.
Danny BoerrigterNeuroscience Research Australia, Randwick, NSW, 2031, Australia.
Helen BallBiostatistics and Bioinformatics Facility, Bosch Institute, The University of Sydney, Sydney, NSW, 2006, Australia.
Cynthia Shannon WeickertNeuroscience Research Australia, Randwick, NSW, 2031, Australia.
Kay L DoubleDiscipline of Biomedical Science and Brain and Mind Centre, Sydney Medical School, The University of Sydney, Sydney, NSW, 2006, Australia.

Funding

Brain Tissue Resource Centre for Alcohol ResearchR28AA012725 · NIAAA · UNIVERSITY OF SYDNEY · PI Greg Trevor Sutherland · 2012 to 2026
$7.0M
NIAAA NIH HHS R28 AA012725
6 · The paper itself

Abstract

Reduced neurogenesis in the aging mammalian hippocampus has been linked to cognitive deficits and increased risk of dementia. We utilized postmortem human hippocampal tissue from 26 subjects aged 18-88 years to investigate changes in expression of six genes representing different stages of neurogenesis across the healthy adult lifespan. Progressive and significant decreases in mRNA levels of the proliferation marker Ki67 (MKI67) and the immature neuronal marker doublecortin (DCX) were found in the healthy human hippocampus over the lifespan. In contrast, expression of genes for the stem cell marker glial fibrillary acidic protein delta and the neuronal progenitor marker eomesodermin was unchanged with age. These data are consistent with a persistence of the hippocampal stem cell population with age. Age-associated expression of the proliferation and immature neuron markers MKI67 and DCX, respectively, was unrelated, suggesting that neurogenesis-associated processes are independently altered at these points in the development from stem cell to neuron. These data are the first to demonstrate normal age-related decreases at specific stages of adult human hippocampal neurogenesis.

Indexed as

AdolescentAdultAgedAged, 80 and overCell DifferentiationCell ProliferationDoublecortin Domain ProteinsDoublecortin ProteinFemaleGene Expression Regulation, DevelopmentalGlial Fibrillary Acidic ProteinHealthy AgingHippocampusHumansKi-67 AntigenMaleDCX protein, humanDoublecortin Domain ProteinsDoublecortin ProteinEOMES protein, humanGlial Fibrillary Acidic ProteinKi-67 AntigenMicrotubule-Associated ProteinsNeuropeptidesT-Box Domain Proteinscognitiondoublecortinhealthy aginghippocampusKi67neurogenesis

Identifiers

PMID28766905
PMCPMC5595679

What OpenQuestion holds

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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 OpenQuestion graph.