Evidence map›Paper›PMID 37043881›Full record

ArticleNeurobiology of aging2023

Annualized changes in rate of amyloid deposition and neurodegeneration are greater in participants who become amyloid positive than those who remain amyloid negative.

Renée C Groechel, Yorghos Tripodis, Michael L Alosco, Jesse Mez, Wei Qiao Qiu, Gustavo Mercier, Lee Goldstein, Andrew E Budson, Neil W Kowall, Ronald J Killiany and 1 more

Abstract read
In one paragraph

Article in Neurobiology of aging, 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
0.9field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

11 authors at 1 institution in 1 country.

Renée C GroechelDepartment of Anatomy & Neurobiology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA. Electronic address: groechelrc@nih.gov.
Yorghos TripodisDepartment of Biostatistics, Boston University School of Public Health, Boston, MA, USA; Boston University Alzheimer's Disease Research Center, Boston, MA, USA.
Michael L AloscoBoston University Alzheimer's Disease Research Center, Boston, MA, USA; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Jesse MezBoston University Alzheimer's Disease Research Center, Boston, MA, USA; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Wei Qiao QiuBoston University Alzheimer's Disease Research Center, Boston, MA, USA; Department of Psychiatry, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Gustavo MercierBoston University Alzheimer's Disease Research Center, Boston, MA, USA; Department of Radiology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Lee GoldsteinBoston University Alzheimer's Disease Research Center, Boston, MA, USA; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Andrew E BudsonBoston University Alzheimer's Disease Research Center, Boston, MA, USA; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Neil W KowallBoston University Alzheimer's Disease Research Center, Boston, MA, USA; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Ronald J KillianyDepartment of Anatomy & Neurobiology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA; Boston University Alzheimer's Disease Research Center, Boston, MA, USA; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA; Department of Radiology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
Alzheimer’s Disease Neuroimaging Initiative
Boston University · US

Funding

Identification and characterization of the CD31-ApoE-mCRP pathway for Alzheimer's disease in humans.RF1AG075832 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI EMILI, ANDREW, QIU, WEI QIAO WENDY · 2023 to 2023
$2.4M
NIA NIH HHS RF1 AG075832
6 · The paper itself

Abstract

This study longitudinally examined participants in the Alzheimer's Disease Neuroimaging Initiative (ADNI) who underwent a conversion in amyloid-beta (Aβ) status in comparison to a group of ADNI participants who did not show a change in amyloid status over the same follow-up period. Participants included 136 ADNI dementia-free participants with 2 florbetapir positron emission tomography (PET) scans. Of these participants, 68 showed amyloid conversion as measured on florbetapir PET, and the other 68 did not. Amyloid converters and non-converters were chosen to have representative demographic data (age, education, sex, diagnostic status, and race). The amyloid converter group showed increased prevalence of APOE ε4 (p < 0.001), greater annualized percent volume loss in selected magnetic resonance imaging (MRI) regions (p < 0.05), lower cerebrospinal fluid Aβ

Indexed as

Alzheimer DiseaseCognitive DysfunctionAmyloidAmyloid beta-PeptidesAniline CompoundsBrainEthylene GlycolsHumansPositron-Emission TomographyAmyloidAmyloid beta-PeptidesAniline CompoundsEthylene GlycolsflorbetapirAlzheimer’s diseaseAmyloidCognitionDementiaMagnetic resonance imagingPositron emission tomography

Identifiers

PMID37043881
PMCPMC13168552
OpenAlexW4323655072

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.