Evidence map›Paper›PMID 37885919›Full record

ArticleAlzheimer's & dementia (Amsterdam, Netherlands)

Cross-sectional and longitudinal evaluation of plasma glial fibrillary acidic protein to detect and predict clinical syndromes of Alzheimer's disease.

Madeline Ally, Michael A Sugarman, Henrik Zetterberg, Kaj Blennow, Nicholas J Ashton, Thomas K Karikari, Hugo J Aparicio, Brandon Frank, Yorghos Tripodis, Brett Martin and 18 more

Open access · goldAbstract 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. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
6.2field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

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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

28 authors at 4 institutions in 5 countries.

Madeline AllyBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Michael A SugarmanBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Henrik ZetterbergDepartment of Neurodegenerative Disease UCL Institute of Neurology London UK.
Kaj BlennowClinical Neurochemistry Laboratory Sahlgrenska University Hospital Mölndal Sweden.
Nicholas J AshtonDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology The Sahlgrenska Academy at the University of Gothenburg Gothenburg Sweden.
Thomas K KarikariClinical Neurochemistry Laboratory Sahlgrenska University Hospital Mölndal Sweden.
Hugo J AparicioBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Brandon FrankBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Yorghos TripodisBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Brett MartinBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Joseph N PalmisanoBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Eric G SteinbergBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Irene SimkinDepartment of Medicine Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Lindsay A FarrerBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Gyungah R JunDepartment of Medicine Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Katherine W TurkBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Andrew E BudsonBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Maureen K O'ConnorBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Rhoda AuBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Lee E GoldsteinBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Neil W KowallBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Ronald KillianyBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Robert A SternBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Thor D SteinBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Ann C McKeeBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Wei Qiao QiuBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Jesse MezBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Michael L AloscoBoston University Alzheimer's Disease Research Center and CTE Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA.
Boston University · USSahlgrenska University Hospital · SEKing's College London · GBUniversity of Pittsburgh · US

Funding

Project-005UL1TR001430 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BAIR-MERRITT, MEGAN H, CENTER, DAVID M. · 2015 to 2024
$52.3M
RL5: Research Education CoreP30AG072978 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Lindsay A. Farrer · 2021 to 2026
$25.6M
Plasma brain-derived tau: a novel Alzheimer’s disease-type neurodegeneration biomarker with potential to complete the AT(N) scheme in bloodR01AG083874 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Thomas K Karikari · 2023 to 2026
$14.5M
The effects of iron on oxidative stress and Alzheimer's biomarkers in amyloid-positive and negative elderly normalR01AG068398 · NIA · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHIANG, GLORIA CHIA-YI · 2020 to 2024
$2.8M
Repetitive Head Impact Exposure and Later-Life White Matter Signal Abnormalities: An Investigation in Former NFL Players, Subjects with Alzheimer's Disease, and Cognitively Normal ControlsK23NS102399 · NINDS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ALOSCO, MICHAEL · 2018 to 2022
$793k
CSRD VA IK2 CX002065NCATS NIH HHS UL1 TR001430NIA NIH HHS P30 AG072978NIA NIH HHS R01 AG068398NIA NIH HHS R01 AG083874NINDS NIH HHS K23 NS102399
6 · The paper itself

Abstract

Introduction: This study examined plasma glial fibrillary acidic protein (GFAP) as a biomarker of cognitive impairment due to Alzheimer's disease (AD) with and against plasma neurofilament light chain (NfL), and phosphorylated tau (p-tau) Methods: Plasma samples were analyzed using Simoa platform for 567 participants spanning the AD continuum. Cognitive diagnosis, neuropsychological testing, and dementia severity were examined for cross-sectional and longitudinal outcomes. Results: Plasma GFAP discriminated AD dementia from normal cognition (adjusted mean difference = 0.90 standard deviation [SD]) and mild cognitive impairment (adjusted mean difference = 0.72 SD), and demonstrated superior discrimination compared to alternative plasma biomarkers. Higher GFAP was associated with worse dementia severity and worse performance on 11 of 12 neuropsychological tests. Longitudinally, GFAP predicted decline in memory, but did not predict conversion to mild cognitive impairment or dementia. Discussion: Plasma GFAP was associated with clinical outcomes related to suspected AD and could be of assistance in a plasma biomarker panel to detect in vivo AD.

Indexed as

Alzheimer's diseaseglial fibrillary acidic proteinneurofilament light chainneuropsychologyphosphorylated tauplasma biomarkers

Identifiers

PMID37885919
PMCPMC10599277
OpenAlexW4387965067

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.