Evidence map›Paper›PMID 42824090›Full record

ArticleAlzheimer's & dementia (Amsterdam, Netherlands)

Evaluation of plasma neurofilament and glial fibrillary acidic protein to predict or detect amyloid related imaging abnormalities.

Nicholas U Schwartz, Tara Ellingson, Hong Nguyen, Zoe Lin, Nicholas J Ashton, Jeffrey L Dage, Kaancan Deniz, Connor D Dietz, Peter A Ljubenkov, Bruce L Miller and 14 more

Abstract read
In one paragraph

Article in Alzheimer's & dementia (Amsterdam, Netherlands). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

24 authors.

Nicholas U SchwartzEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.ORCID https://orcid.org/0000-0003-1040-7819
Tara EllingsonEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Hong NguyenEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Zoe LinEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Nicholas J AshtonBanner Sun Health Research Institute Sun City Arizona USA.
Jeffrey L DageDepartment of Neurology Indiana University School of Medicine Indianapolis Indiana USA.
Kaancan DenizEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Connor D DietzEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Peter A LjubenkovEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Bruce L MillerEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Kambiz NaelDepartment of Radiology & Biomedical Imaging Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Katherine PossinEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Julio C RojasEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Howie J RosenEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Rowan SalonerEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
David N Soleimani-MeigooniEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Adam M StaffaroniEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Melanie L StephensEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Gautam TammewarEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Yingbing WangDepartment of Radiology & Biomedical Imaging Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Renaud La JoieEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Gil D RabinoviciEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Adam L BoxerEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.
Lawren VandeVredeEdward and Pearl Fein Memory and Aging Center Department of Neurology Weill Institute for Neurosciences University of California, San Francisco San Francisco California USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAmyloid-targeting therapies (ATT) require frequent magnetic resonance imaging monitoring to detect vasogenic edema and hemorrhage, i.e., amyloid-related imaging abnormalities (ARIA). Neurofilament light chain (NfL) and glial fibrillary acidic protein (GFAP) are potential blood-based biomarkers (BBM) of ARIA.

methodsPlasma NfL and GFAP were longitudinally collected in an ATT clinic and natural log transformed. Baseline, pre-ARIA, and trajectories were compared between patients with (

resultsBaseline NfL and GFAP did not differ between patients with or without ARIA (ln[NfL] ECLIA 1.24 ± 0.38 pg/mL vs 1.25 ± 0.40 pg/mL, DISCUSSION: Biobanking in treatment clinics can evaluate clinical utility of BBMs as monitoring tools. These findings do not support a strong association between NfL or GFAP and ARIA in the ATT clinic.

Indexed as

Alzheimer's diseaseAlzheimer's treatment clinicamyloid‐related imaging abnormalities (ARIA)amyloid‐targeting therapyanti‐amyloidbiomarkerglial fibrillary acidic protein (GFAP)neurofilament light chain (NfL)real‐world

Identifiers

PMID42824090
PMCPMC13627248

What Socratic holds

Textmetadata
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 Socratic graph.