Evidence map›Paper›PMID 27834774›Full record

ArticleJournal of Alzheimer's disease : JAD2017

Five-Year Longitudinal Brain Volume Change in Healthy Elders at Genetic Risk for Alzheimer's Disease.

Katherine Reiter, Kristy A Nielson, Sally Durgerian, John L Woodard, J Carson Smith, Michael Seidenberg, Dana A Kelly, Stephen M Rao

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Metabolic, demographic, and behavioral risk factors predict brain structural variability in the general population: an analysis of the human connectome project young adults.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
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  11. Structural and functional imaging of brains.Science China. Chemistry · 2023
    Review
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  16. Review
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  19. Older, non-demented apolipoprotein εNeurobiology of aging · 2020
    Article
  20. Observational
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

8 authors.

Katherine ReiterDepartment of Psychology, Marquette University, Milwaukee, WI, USA.
Kristy A NielsonDepartment of Psychology, Marquette University, Milwaukee, WI, USA.
Sally DurgerianDepartment of Neurology, Medical College of Wisconsin, Milwaukee, WI, USA.
John L WoodardDepartment of Psychology, Wayne State University, Detroit, MI, USA.
J Carson SmithDepartment of Kinesiology, School of Public Health, University of Maryland, College Park, MD, USA.
Michael SeidenbergDepartment of Psychology, Rosalind Franklin University, North Chicago, IL, USA.
Dana A KellyDepartment of Psychology, Rosalind Franklin University, North Chicago, IL, USA.
Stephen M RaoSchey Center for Cognitive Neuroimaging, Lou Ruvo Center for Brain Health, Neurological Institute, Cleveland Clinic, Cleveland, OH, USA.

Funding

ZONISMIDE IN THE TREATMENT OF SEIZURES IN PATIENTSM01RR000058 · NCRR · MEDICAL COLLEGE OF WISCONSIN · PI FRANKLIN, SUZIE · 1985 to 2006
$19.9M
Immune Mechanisms Underlying the Neuroprotective Effects of Physical Activity in Human and Mouse Models of Genetic Risk for Alzheimers DiseaseR01AG022304 · NIA · MEDICAL COLLEGE OF WISCONSIN · PI LAMB, BRUCE T, RAO, STEPHEN MARK · 2003 to 2021
$13.0M
NCRR NIH HHS M01 RR000058NIA NIH HHS R01 AG022304
6 · The paper itself

Abstract

Neuropathological changes associated with Alzheimer's disease (AD) precede symptom onset by more than a decade. Possession of an apolipoprotein E (APOE) ɛ4 allele is the strongest genetic risk factor for late onset AD. Cross-sectional studies of cognitively intact elders have noted smaller hippocampal/medial temporal volumes in ɛ4 carriers (ɛ4+) compared to ɛ4 non-carriers (ɛ4-). Few studies, however, have examined long-term, longitudinal, anatomical brain changes comparing healthy ɛ4+ and ɛ4- individuals. The current five-year study examined global and regional volumes of cortical and subcortical grey and white matter and ventricular size in 42 ɛ4+ and 30 ɛ4- individuals. Cognitively intact participants, ages 65-85 at study entry, underwent repeat anatomical MRI scans on three occasions: baseline, 1.5, and 4.75 years. Results indicated no between-group volumetric differences at baseline. Over the follow-up interval, the ɛ4+ group experienced a greater rate of volume loss in total grey matter, bilateral hippocampi, right hippocampal subfields, bilateral lingual gyri, bilateral parahippocampal gyri, and right lateral orbitofrontal cortex compared to the ɛ4- group. Greater loss in grey matter volumes in ɛ4+ participants were accompanied by greater increases in lateral, third, and fourth ventricular volumes. Rate of change in white matter volumes did not differentiate the groups. The current results indicate that longitudinal measurements of brain atrophy can serve as a sensitive biomarker for identifying neuropathological changes in persons at genetic risk for AD and potentially, for assessing the efficacy of treatments designed to slow or prevent disease progression during the preclinical stage of AD.

Indexed as

AgedAged, 80 and overAgingAlzheimer DiseaseApolipoprotein E4AtrophyBrainCognition DisordersFemaleFunctional LateralityHumansImage Processing, Computer-AssistedLateral VentriclesLongitudinal StudiesMagnetic Resonance ImagingMaleApolipoprotein E4Alzheimer’s diseaseApoE4longitudinal studiesMRI scans

Identifiers

PMID27834774
PMCPMC5924681

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.