Evidence map›Paper›PMID 33835624›Full record

ArticleHippocampus2021

APOE moderates the effect of hippocampal blood flow on memory pattern separation in clinically normal older adults.

Molly Memel, Adam M Staffaroni, Yann Cobigo, Kaitlin B Casaletto, Corrina Fonseca, Brianne M Bettcher, Michael A Yassa, Fanny M Elahi, Amy Wolf, Howard J Rosen and 1 more

Open access · greenAbstract read
In one paragraph

Article in Hippocampus, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

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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

11 authors at 4 institutions in 1 country.

Molly MemelSan Francisco VA Medical Center, San Francisco, California, USA.ORCID 0000-0001-6827-6335
Adam M StaffaroniDepartment of Neurology, Memory and Aging Center, University of California, San Francisco (UCSF), San Francisco, California, USA.
Yann CobigoDepartment of Neurology, Memory and Aging Center, University of California, San Francisco (UCSF), San Francisco, California, USA.
Kaitlin B CasalettoDepartment of Neurology, Memory and Aging Center, University of California, San Francisco (UCSF), San Francisco, California, USA.
Corrina FonsecaDepartment of Neurology, Memory and Aging Center, University of California, San Francisco (UCSF), San Francisco, California, USA.
Brianne M BettcherDepartment of Neurology, University of Colorado Anschutz Medical Campus, CU Alzheimer's and Cognition Center, Aurora, Colorado, USA.
Michael A YassaDepartment of Neurobiology and Behavior and Center for the Neurobiology of Learning and Memory, University of California, Irvine, California, USA.
Fanny M ElahiDepartment of Neurology, Memory and Aging Center, University of California, San Francisco (UCSF), San Francisco, California, USA.
Amy WolfDepartment of Neurology, Memory and Aging Center, University of California, San Francisco (UCSF), San Francisco, California, USA.
Howard J RosenDepartment of Neurology, Memory and Aging Center, University of California, San Francisco (UCSF), San Francisco, California, USA.
Joel H KramerDepartment of Neurology, Memory and Aging Center, University of California, San Francisco (UCSF), San Francisco, California, USA.
University of California, San Francisco · USSan Francisco VA Medical Center · USUniversity of California, Irvine · USUniversity of Colorado Anschutz Medical Campus · US

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Merrilees · 2002 to 2026
$67.2M
PrPSc SPECIFIC INTERACTION WITH NOVEL PrP-Fc FUSION PROTEINSP50AG023501 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MILLER, BRUCE L · 2004 to 2018
$27.1M
Mechanisms of Executive Decline in Normal AgingR01AG032289 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Kaitlin B Casaletto, JOEL H KRAMER · 2009 to 2026
$8.3M
Investigating the Contribution of Peripheral versus Central Nervous System Immune Dysfunction to Cognitive AgingR01AG058772 · NIA · UNIVERSITY OF COLORADO DENVER · PI BETTCHER, BRIANNE MAGOUIRK · 2019 to 2023
$3.7M
Novel imaging and endothelial biomarkers of small vessel cerebrovascular diseaseUH3NS100608 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DECARLI, CHARLES, KRAMER, JOEL H · 2018 to 2020
$3.5M
Effects of chronic inflammation on brain structure and functionR01AG048234 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRAMER, JOEL H · 2015 to 2019
$3.2M
Novel Imaging and Biofluid Biomarkers of Small Vessel Cerebrovascular DiseaseUF1NS100608 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRAMER, JOEL H · 2021 to 2021
$2.5M
Multimodal Imaging in Frontotemporal DegenerationK24AG045333 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSEN, HOWARD J · 2013 to 2023
$1.9M
Can Behavior Shape Neural Health? Identifying Modifiable Factors to Prevent Cognitive Decline in AgeK23AG058752 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CASALETTO, KAITLIN B · 2018 to 2022
$994k
Optimizing Clinical Trial Endpoints in Frontotemporal DementiaK23AG061253 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STAFFARONI, ADAM MARK · 2019 to 2023
$946k
CSRD VA IK2 CX002180NIA NIH HHS K23 AG058752NIA NIH HHS K23 AG061253NIA NIH HHS K24 AG045333NIA NIH HHS P01 AG019724NIA NIH HHS P50 AG023501NIA NIH HHS R01 AG032289NIA NIH HHS R01 AG048234NIA NIH HHS R01 AG058772NINDS NIH HHS UF1 NS100608NINDS NIH HHS UH3 NS100608
6 · The paper itself

Abstract

Pattern separation, the ability to differentiate new information from previously experienced similar information, is highly sensitive to hippocampal structure and function and declines with age. Functional MRI studies have demonstrated hippocampal hyperactivation in older adults compared to young, with greater task-related activation associated with worse pattern separation performance. The current study was designed to determine whether pattern separation was sensitive to differences in task-free hippocampal cerebral blood flow (CBF) in 130 functionally intact older adults. Given prior evidence that apolipoprotein E e4 (APOE e4) status moderates the relationship between CBF and episodic memory, we predicted a stronger negative relationship between hippocampal CBF and pattern separation in APOE e4 carriers. An interaction between APOE group and right hippocampal CBF was present, such that greater right hippocampal CBF was related to better lure discrimination in noncarriers, whereas the effect reversed directionality in e4 carriers. These findings suggest that neurovascular changes in the medial temporal lobe may underlie memory deficits in cognitively normal older adults who are APOE e4 carriers.

Indexed as

Apolipoprotein E4HippocampusAgedAgingApolipoproteins ECerebrovascular CirculationHumansMagnetic Resonance ImagingNeuropsychological TestsRegional Blood FlowTemporal LobeApolipoprotein E4Apolipoproteins EAPOEASL perfusionhippocampuspattern separation

Identifiers

PMID33835624
PMCPMC8295213
OpenAlexW3148677021

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.