Evidence mapPaperPMID 37224404Full record

ArticleJournal of clinical and experimental neuropsychology2023

Change on the Repeatable Battery for the Assessment of Neuropsychological Status and its relationship to brain amyloid.

Kevin Duff, Ava M Dixon, Lindsay Embree, John M Hoffman

Abstract read
In one paragraph

Article in Journal of clinical and experimental neuropsychology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Trial
  2. 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

4 authors.

Kevin DuffLayton Aging and Alzheimer's Disease Center, Department of Neurology, Oregon Health & Science University, Portland, OR, United States.ORCID 0000-0002-9336-2400
Ava M DixonCenter for Alzheimer's Care, Imaging and Research, Department of Neurology, University of Utah, Salt Lake City, UT, United States.
Lindsay EmbreeCenter for Alzheimer's Care, Imaging and Research, Department of Neurology, University of Utah, Salt Lake City, UT, United States.
John M HoffmanCenter for Quantitative Cancer Imaging, Huntsman Cancer Institute, Salt Lake City, UT, USA.

Funding

UNIVERSITY OF UTAH CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCE-UL1: BPCAUL1RR025764 · NCRR · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2008 to 2011
$19.4M
University of Utah Center for Clinical and Translational Science-UL1UL1TR000105 · NCATS · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2012 to 2013
$5.1M
Enriching clinical trials requiring amyloid positivity with practice effectsR01AG055428 · NIA · UNIVERSITY OF UTAH · PI DUFF, KEVIN M, HOFFMAN, JOHN M · 2017 to 2021
$3.6M
NCATS NIH HHS UL1 TR000105NCRR NIH HHS UL1 RR025764NIA NIH HHS R01 AG055428
6 · The paper itself

Abstract

backgroundThe Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) has been associated with commonly used biomarkers of Alzheimer's disease (AD), including brain amyloid plaque density. However, less is known about if changes in the RBANS across time are also related to brain amyloid deposition. The current study sought to expand on prior work by examining the relationship between changes over time on the RBANS and amyloid deposition via positron emission tomography (PET).

methodOne-hundred twenty-six older adults with intact or impaired cognition and daily functioning underwent repeat assessment with the RBANS across nearly 16 months, as well as had a baseline amyloid PET scan.

resultsIn the entire sample, amyloid deposition was significantly related to change on all five Indexes and the Total Scale score of the RBANS, with greater amyloid being associated with worsening cognition. This pattern was also observed in 11 of 12 subtests.

conclusionsWhereas prior studies have identified a relationship between baseline RBANS and amyloid status, the current findings support that changes in the RBANS are also indicative of AD brain pathology, even if these findings are mediated by cognitive status. Although replication in a more diverse sample is needed, these results continue to support the use of the RBANS in AD clinical trials.

Indexed as

Alzheimer DiseaseCognition DisordersCognitive DysfunctionAgedBrainHumansNeuropsychological TestsAlzheimer’s diseaseamyloidbrain imagingmild cognitive impairmentneuropsychological testing

Identifiers

PMID37224404
PMCPMC10330480

What Socratic holds

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Registered trials

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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 Socratic graph.