Evidence map›Paper›PMID 32538837›Full record

ArticleJournal of Alzheimer's disease : JAD2020

Genetic Risk for Alzheimer's Disease Moderates the Association Between Medial Temporal Lobe Volume and Episodic Memory Performance Among Older Adults.

Sarah Prieto, Kate E Valerio, Jena N Moody, Scott M Hayes, Jasmeet P Hayes, Alzheimer’s Disease Neuroimaging Initiative

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. The impact of polygenic risk for alzheimer's disease on neurotransmitter-related grey matter atrophy in the alzheimer continuum.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
  3. Article
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.

Sarah PrietoDepartment of Psychology, The Ohio State University, Columbus, OH, USA.
Kate E ValerioDepartment of Psychology, The Ohio State University, Columbus, OH, USA.
Jena N MoodyDepartment of Psychology, The Ohio State University, Columbus, OH, USA.
Scott M HayesDepartment of Psychology, The Ohio State University, Columbus, OH, USA.
Jasmeet P HayesDepartment of Psychology, The Ohio State University, Columbus, OH, USA.
Alzheimer’s Disease Neuroimaging Initiative

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
Neuroimaging and Molecular Markers of AD and Neurodegenerative Disease after ConcussionR01AG058822 · NIA · OHIO STATE UNIVERSITY · PI Jasmeet Pannu Hayes · 2019 to 2026
$2.7M
Exploring real-time alterations in cerebral perfusion, BOLD signal, and cognition during physical activityR21AG056921 · NIA · OHIO STATE UNIVERSITY · PI HAYES, SCOTT M · 2018 to 2019
$409k
NIA NIH HHS R01 AG058822NIA NIH HHS R21 AG056921NIA NIH HHS U01 AG024904
6 · The paper itself

Abstract

backgroundA complex set of interactions between biological, genetic, and environmental factors likely underlies the development of Alzheimer's disease (AD). Identifying which of these factors is most associated with AD is important for early diagnosis and treatment.

objectiveWe sought to examine genetic risk and structural brain volume on episodic memory in a sample of older adults ranging from cognitively normal to those diagnosed with AD.

methods686 adults (55-91 years old) completed a 3T MRI scan, baseline cognitive assessments, and biospecimen collection through the Alzheimer's Disease Neuroimaging Initiative. Hierarchical linear regression analyses examined main and interaction effects of medial temporal lobe (MTL) volume and polygenic hazard score (PHS), indicating genetic risk for AD, on a validated episodic memory composite score.

resultsGenetic risk moderated the relationship between MTL volume and memory, such that individuals with high PHS and lower hippocampal and entorhinal volume had lower memory composite scores [ΔF (1,677) = 4.057, p = 0.044, ΔR2 = 0.002]. Further analyses showed this effect was driven by the left hippocampus [ΔF(1,677) = 5.256, p = 0.022, ΔR2 = 0.003] and right entorhinal cortex [ΔF (1,677) = 6.078, p = 0.014, ΔR2 = 0.003].

conclusionsAmong those with high genetic risk for AD, lower volume was associated with poorer memory. Results suggest that the interaction between AD genetic risk and MTL volume increases the likelihood for memory impairment among older adults. Results from this study suggest that genetic risk and brain volume should be considered key factors in tracking cognitive decline.

Indexed as

Memory, EpisodicAgedAged, 80 and overAlzheimer DiseaseFemaleGenetic Predisposition to DiseaseHumansMagnetic Resonance ImagingMaleMiddle AgedOrgan SizePositron-Emission TomographyPsychomotor PerformanceTemporal LobeAlzheimer’s diseaseatrophyentorhinal cortexepisodic memoryhippocampusmedial temporal lobepolygenic risk

Identifiers

PMID32538837
PMCPMC7558431

What OpenQuestion holds

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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.