Evidence map›Paper›PMID 32239141›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2020

Functional Connectivity of Hippocampal CA3 Predicts Neurocognitive Aging via CA1-Frontal Circuit.

Xia Liang, Li-Ming Hsu, Hanbing Lu, Jessica A Ash, Peter R Rapp, Yihong Yang

Open access · bronzeAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. The effects ofIBRO neuroscience reports · 2026
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  11. Cognitive aging is associated with redistribution of synaptic weights in the hippocampus.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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 4 institutions in 2 countries.

Xia LiangLaboratory for Space Environment and Physical Sciences, Harbin Institute of Technology, Harbin 150001, China.
Li-Ming HsuNeuroimaging Research Branch, National Institute on Drug Abuse, Biomedical Research Center, National Institutes of Health (NIH), Baltimore, MD 21224, USA.
Hanbing LuNeuroimaging Research Branch, National Institute on Drug Abuse, Biomedical Research Center, National Institutes of Health (NIH), Baltimore, MD 21224, USA.
Jessica A AshLaboratory of Behavioral Neuroscience, National Institute on Aging, Biomedical Research Center, NIH, Baltimore, MD 21224, USA.
Peter R RappLaboratory of Behavioral Neuroscience, National Institute on Aging, Biomedical Research Center, NIH, Baltimore, MD 21224, USA.
Yihong YangNeuroimaging Research Branch, National Institute on Drug Abuse, Biomedical Research Center, National Institutes of Health (NIH), Baltimore, MD 21224, USA.
National Institute on Aging · USNational Institutes of Health · USHarbin Institute of Technology · CNNational Institute on Drug Abuse · US

Funding

Neurocognitive Aging: Experience-Dependent Dynamics, Plasticity and Network ContributionsZIAAG000350 · NIA · NATIONAL INSTITUTE ON AGING · PI RAPP, PETER R · 2009 to 2025
$30.9M
Neuroimaging of animal models of neurologic and psychiatric disordersZIADA000572 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI YANG, YIHONG · 2010 to 2020
$9.3M
6 · The paper itself

Abstract

The CA3 and CA1 principal cell fields of the hippocampus are vulnerable to aging, and age-related dysfunction in CA3 may be an early seed event closely linked to individual differences in memory decline. However, whether the differential vulnerability of CA3 and CA1 is associated with broader disruption in network-level functional interactions in relation to age-related memory impairment, and more specifically, whether CA3 dysconnectivity contributes to the effects of aging via CA1 network connectivity, has been difficult to test. Here, using resting-state fMRI in a group of aged rats uncontaminated by neurodegenerative disease, aged rats displayed widespread reductions in functional connectivity of CA3 and CA1 fields. Age-related memory deficits were predicted by connectivity between left CA3 and hippocampal circuitry along with connectivity between left CA1 and infralimbic prefrontal cortex. Notably, the effects of CA3 connectivity on memory performance were mediated by CA1 connectivity with prefrontal cortex. We additionally found that spatial learning and memory were associated with functional connectivity changes lateralized to the left CA3 and CA1 divisions. These results provide novel evidence that network-level dysfunction involving interactions of CA3 with CA1 is an early marker of poor cognitive outcome in aging.

Indexed as

AgingAnimalsBrain MappingCA1 Region, HippocampalCA3 Region, HippocampalMagnetic Resonance ImagingMaleMemoryNeural PathwaysPrefrontal CortexRatsRats, Long-EvansSpatial Learningagingfunctional connectivityhippocampusspatial memory

Identifiers

PMID32239141
PMCPMC7325802
OpenAlexW3014381293

What OpenQuestion holds

Textmetadata
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.