Evidence map›Paper›PMID 23069756›Full record

ReviewNeuroscience2013

Dendritic spine changes associated with normal aging.

D L Dickstein, C M Weaver, J I Luebke, P R Hof

Abstract readReview
In one paragraph

Review in Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 174 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
174citing papers in PubMed, 2 pooled it
–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

174 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. The endocannabinoid system and the ageing brain.Nature reviews. Neuroscience · 2026
    Review
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  18. ACSS2 upregulation enhances neuronal resilience to aging and tau-associated neurodegeneration.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  20. Article

114 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

4 authors.

D L DicksteinFishberg Department of Neuroscience, Friedman Brain Institute, Mount Sinai School of Medicine, New York, NY 10029, USA; Computational Neurobiology and Imaging Center, Mount Sinai School of Medicine, New York, NY 10029, USA. Electronic address: dara.dickstein@mssm.edu.
C M Weaver
J I Luebke
P R Hof

Funding

STRUCTURAL STUDIES IN THE CENTRAL NERVOUS SYSTEMP01AG000001 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ROSENE, DOUGLAS L · 1985 to 2013
$20.7M
Modeling Cellular Determinants of Cognitive Decline in AgingR01AG035071 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HOF, PATRICK R, WEAVER, CHRISTINA M · 2010 to 2014
$1.9M
Multiscale Analysis of Neuronal MorphologyR01MH071818 · NIMH · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI HOF, PATRICK R · 2005 to 2009
$1.6M
AGE-RELATED CHANGES IN MONKEY CORTICAL PYRAMIDAL CELLSR01AG025062 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LUEBKE, JENNIFER I · 2005 to 2009
$1.5M
NIA NIH HHS AG00001NIA NIH HHS AG025062NIA NIH HHS AG035071NIA NIH HHS P01 AG000001NIA NIH HHS R01 AG025062NIA NIH HHS R01 AG035071NIMH NIH HHS MH071818NIMH NIH HHS R01 MH071818
6 · The paper itself

Abstract

Given the rapid rate of population aging and the increased incidence of cognitive decline and neurodegenerative diseases with advanced age, it is important to ascertain the determinants that result in cognitive impairment. It is also important to note that much of the aged population exhibit 'successful' cognitive aging, in which cognitive impairment is minimal. One main goal of normal aging studies is to distinguish the neural changes that occur in unsuccessful (functionally impaired) subjects from those of successful (functionally unimpaired) subjects. In this review, we present some of the structural adaptations that neurons and spines undergo throughout normal aging and discuss their likely contributions to electrophysiological properties and cognition. Structural changes of neurons and dendritic spines during aging, and the functional consequences of such changes, remain poorly understood. Elucidating the structural and functional synaptic age-related changes that lead to cognitive impairment may lead to the development of drug treatments that can restore or protect neural circuits and mediate cognition and successful aging.

Indexed as

AgingAnimalsBrainCognitionDendritic SpinesHumansNeuronal PlasticityNeuronsagingcAMPChATcholine acetyltransferasecognitioncyclic-AMPdelayed non-matching-to-sampledelayed recognition span testdendritic spinesdentate gyrusDGDNMSDRSTelectrophysiologyGluRglutamate receptorsHCNhyperpolarization-activated cyclic nucleotide-gatedmorphologyNMDAN-methyl-d-aspartateovariectomizedOVXPFCPKCpostsynaptic currentsprefrontal cortexprotein kinase CPSCsSAMPsenescence-prone strains

Identifiers

PMID23069756
PMCPMC3654095

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.