Evidence map›Paper›PMID 38012799›Full record

ArticleAlzheimer's research & therapy2023

Clinical outcomes up to 9 years after [

Lyduine E Collij, Gill Farrar, Marissa Zwan, Elsmarieke van de Giessen, Rik Ossenkoppele, Frederik Barkhof, Annemieke J M Rozemuller, Yolande A L Pijnenburg, Wiesje M van der Flier, Femke Bouwman

Abstract read
In one paragraph

Article in Alzheimer's research & therapy, 2023. 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. Review
  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

10 authors.

Lyduine E CollijDepartment of Radiology and Nuclear Medicine, Amsterdam UMC - location VUmc, Amsterdam, The Netherlands. l.collij@amsterdamumc.nl.
Gill FarrarGE Healthcare, Amersham, UK.
Marissa ZwanAlzheimer Center and Department of Neurology, Amsterdam UMC - location VUmc, Amsterdam, The Netherlands.
Elsmarieke van de GiessenDepartment of Radiology and Nuclear Medicine, Amsterdam UMC - location VUmc, Amsterdam, The Netherlands.
Rik OssenkoppeleClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
Frederik BarkhofDepartment of Radiology and Nuclear Medicine, Amsterdam UMC - location VUmc, Amsterdam, The Netherlands.
Annemieke J M RozemullerDepartment of Pathology, Amsterdam UMC - Location VUmc, Amsterdam, The Netherlands.
Yolande A L PijnenburgAlzheimer Center and Department of Neurology, Amsterdam UMC - location VUmc, Amsterdam, The Netherlands.
Wiesje M van der FlierAlzheimer Center and Department of Neurology, Amsterdam UMC - location VUmc, Amsterdam, The Netherlands.
Femke BouwmanAlzheimer Center and Department of Neurology, Amsterdam UMC - location VUmc, Amsterdam, The Netherlands.

Funding

ZonMw 73305095007
6 · The paper itself

Abstract

backgroundPrevious studies demonstrated increases in diagnostic confidence and change in patient management after amyloid-PET. However, studies investigating longitudinal outcomes over an extended period of time are limited. Therefore, we aimed to investigate clinical outcomes up to 9 years after amyloid-PET to support the clinical validity of the imaging technique.

methodsWe analyzed longitudinal data from 200 patients (M

resultsAt baseline, 184 (92.0%) patients were considered to have dementia. The majority of VR + patients had a primary etiological diagnosis of AD (122/128, 95.3%), while the VR - group consisted mostly of non-AD etiologies, most commonly frontotemporal lobar degeneration (30/72, 40.2%). Overall mortality rate was 48.5% and did not differ between VR - and VR + patients. eDx at follow-up was consistent with baseline diagnosis for 92/108 (85.2%) patients, with most changes observed in VR - cases (VR -  = 14/35, 40% vs VR +  = 2/73, 2.7%, χ

conclusionIn a symptomatic population, we observed that amyloid-status did not impact mortality rates, but is predictive of cognitive functioning over time across several domains. Also, we show particular validity for a negative amyloid-PET assessment, as these patients did not receive an AD diagnosis at follow-up.

Indexed as

Alzheimer DiseaseCognitive DysfunctionAmyloidAmyloid beta-PeptidesAmyloidogenic ProteinsAniline CompoundsBenzothiazolesBrainFemaleHumansMalePositron-Emission TomographyAmyloidAmyloid beta-PeptidesAmyloidogenic ProteinsAniline CompoundsBenzothiazolesflutemetamol[18F]flutemetamol amyloid-PETDiagnosisEarly-onset dementiaNeuropathologySurvival

Identifiers

PMID38012799
PMCPMC10680192

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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 OpenQuestion graph.