Evidence map›Paper›PMID 23897875›Full record

ReviewNeurology2013

Imaging markers for Alzheimer disease: which vs how.

Giovanni B Frisoni, Martina Bocchetta, Gael Chételat, Gil D Rabinovici, Mony J de Leon, Jeffrey Kaye, Eric M Reiman, Philip Scheltens, Frederik Barkhof, Sandra E Black and 16 more

Abstract readComparative StudyReview
In one paragraph

Review in Neurology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed, 4 pooled it
–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

90 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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  9. Simultaneous multiple post-labelling delay ASL MRI and [European journal of nuclear medicine and molecular imaging · 2026
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30 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors.

Giovanni B FrisoniLENITEM-Laboratory of Epidemiology, Neuroimaging and Telemedicine, IRCCS, S. Giovanni di Dio, Fatebenefratelli Brescia, Italy. gfrisoni@fatebenefratelli.it
Martina Bocchetta
Gael Chételat
Gil D Rabinovici
Mony J de Leon
Jeffrey Kaye
Eric M Reiman
Philip Scheltens
Frederik Barkhof
Sandra E Black
David J Brooks
Maria C Carrillo
Nick C Fox
Karl Herholz
Agneta Nordberg
Clifford R Jack
William J Jagust
Keith A Johnson
Christopher C Rowe
Reisa A Sperling
William Thies
Lars-Olof Wahlund
Michael W Weiner
Patrizio Pasqualetti
Charles Decarli
ISTAART's NeuroImaging Professional Interest Area

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
PSYCHOSOCIAL COREP30AG008051 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MITTELMAN, MARY SHERMAN · 1990 to 2019
$36.1M
Neural and Biochemical Mechanisms of Cognitive AgingR01AG034570 · NIA · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI William J. Jagust · 2009 to 2026
$12.0M
PREDICTORS OF COGNITIVE DECLINE IN NORMAL AGINGR01AG012101 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DE LEON, MONY J., RUSINEK, HENRY · 1993 to 2015
$6.7M
Effects of Chemotherapy on Brain FunctionR01AG025303 · NIA · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI JAGUST, WILLIAM J. · 2006 to 2010
$2.3M
Medical Research Council G0601846Medical Research Council G0801306NIA NIH HHS P30 AG008051NIA NIH HHS R01 AG012101NIA NIH HHS R01 AG025303NIA NIH HHS R01 AG034570NIA NIH HHS U01 AG024904
6 · The paper itself

Abstract

Revised diagnostic criteria for Alzheimer disease (AD) acknowledge a key role of imaging biomarkers for early diagnosis. Diagnostic accuracy depends on which marker (i.e., amyloid imaging, ¹⁸F-fluorodeoxyglucose [FDG]-PET, SPECT, MRI) as well as how it is measured ("metric": visual, manual, semiautomated, or automated segmentation/computation). We evaluated diagnostic accuracy of marker vs metric in separating AD from healthy and prognostic accuracy to predict progression in mild cognitive impairment. The outcome measure was positive (negative) likelihood ratio, LR+ (LR-), defined as the ratio between the probability of positive (negative) test outcome in patients and the probability of positive (negative) test outcome in healthy controls. Diagnostic LR+ of markers was between 4.4 and 9.4 and LR- between 0.25 and 0.08, whereas prognostic LR+ and LR- were between 1.7 and 7.5, and 0.50 and 0.11, respectively. Within metrics, LRs varied up to 100-fold: LR+ from approximately 1 to 100; LR- from approximately 1.00 to 0.01. Markers accounted for 11% and 18% of diagnostic and prognostic variance of LR+ and 16% and 24% of LR-. Across all markers, metrics accounted for an equal or larger amount of variance than markers: 13% and 62% of diagnostic and prognostic variance of LR+, and 29% and 18% of LR-. Within markers, the largest proportion of diagnostic LR+ and LR- variability was within ¹⁸F-FDG-PET and MRI metrics, respectively. Diagnostic and prognostic accuracy of imaging AD biomarkers is at least as dependent on how the biomarker is measured as on the biomarker itself. Standard operating procedures are key to biomarker use in the clinical routine and drug trials.

Indexed as

Alzheimer DiseaseBiomarkersFluorodeoxyglucose F18HumansMagnetic Resonance ImagingRadiographyTomography, Emission-Computed, Single-PhotonBiomarkersFluorodeoxyglucose F18

Identifiers

PMID23897875
PMCPMC3776529

What OpenQuestion 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 OpenQuestion graph.