Evidence map›Paper›PMID 29713763›Full record

ReviewEuropean journal of nuclear medicine and molecular imaging2018

Assessing FDG-PET diagnostic accuracy studies to develop recommendations for clinical use in dementia.

Marina Boccardi, Cristina Festari, Daniele Altomare, Federica Gandolfo, Stefania Orini, Flavio Nobili, Giovanni B Frisoni, EANM-EAN Task Force for the Prescription of FDG-PET for Dementing Neurodegenerative Disorders

Open access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in European journal of nuclear medicine and molecular imaging, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
2.4field-weighted citation impact, top 11% 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

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

  1. Pooled it
  2. Outcomes of clinical utility in amyloid-PET studies: state of art and future perspectives.European journal of nuclear medicine and molecular imaging · 2021
    Pooled it
  3. Article
  4. Validating plasma biomarkers for distinguishing neurodegenerative and psychiatric disorders.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  5. Article
  6. Why should academia care about the Target Product Profile?Journal of translational medicine · 2024
    Article
  7. Translational process.Journal of translational medicine · 2023
    Article
  8. Article
  9. Clinical validity of increased cortical uptake of [European journal of nuclear medicine and molecular imaging · 2021
    Review
  10. Clinical impact ofEuropean journal of nuclear medicine and molecular imaging · 2021
    Article
  11. Article
  12. Article
  13. Observational
  14. Clinical utility of FDG-PET for the clinical diagnosis in MCI.European journal of nuclear medicine and molecular imaging · 2018
    Review
  15. Review
  16. Clinical utility of FDG-PET for the differential diagnosis among the main forms of dementia.European journal of nuclear medicine and molecular imaging · 2018
    Review
  17. Review
  18. Article
  19. Clinical utility of FDG-PET in amyotrophic lateral sclerosis and Huntington's disease.European journal of nuclear medicine and molecular imaging · 2018
    Review
  20. Review
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

8 authors at 3 institutions in 3 countries.

Marina BoccardiLANVIE (Laboratoire de Neuroimagerie du Vieillissement), Department of Psychiatry, University of Geneva, Chemin du Petit-Bel-Air, 2, 1225, Chene-Bourg, Geneva, Switzerland. marina.boccardi@unige.ch.ORCID http://orcid.org/0000-0001-6744-8246
Cristina FestariLANE - Laboratory of Alzheimer Neuroimaging & Epidemiology, IRCCS S. Giovanni di Dio, Fatebenefratelli, Brescia, Italy.
Daniele AltomareLANE - Laboratory of Alzheimer Neuroimaging & Epidemiology, IRCCS S. Giovanni di Dio, Fatebenefratelli, Brescia, Italy.
Federica GandolfoAlzheimer Operative Unit; IRCCS Centro S. Giovanni di Dio, Fatebenefratelli, Brescia, Italy.
Stefania OriniAlzheimer Operative Unit; IRCCS Centro S. Giovanni di Dio, Fatebenefratelli, Brescia, Italy.
Flavio NobiliDINOGMI - Department of Neuroscience, University of Genoa and IRCCS Polyclinic San Martino Hospital, Genoa, Italy.
Giovanni B FrisoniLANVIE (Laboratoire de Neuroimagerie du Vieillissement), Department of Psychiatry, University of Geneva, Chemin du Petit-Bel-Air, 2, 1225, Chene-Bourg, Geneva, Switzerland.
EANM-EAN Task Force for the Prescription of FDG-PET for Dementing Neurodegenerative Disorders
Centro San Giovanni di Dio Fatebenefratelli · ITUniversity of Geneva · CHMartin University · US

Funding

European Academy of Neurology n.a.European Association of Nuclear Medicine n.a.
6 · The paper itself

Abstract

backgroundFDG-PET is frequently used as a marker of synaptic damage to diagnose dementing neurodegenerative disorders. We aimed to adapt the items of evidence quality to FDG-PET diagnostic studies, and assess the evidence available in current literature to assist Delphi decisions for European recommendations for clinical use.

methodsBased on acknowledged methodological guidance, we defined the domains, specific to FDG-PET, required to assess the quality of evidence in 21 literature searches addressing as many Population Intervention Comparison Outcome (PICO) questions. We ranked findings for each PICO and fed experts making Delphi decisions for recommending clinical use.

resultsAmong the 1435 retrieved studies, most lacked validated measures of test performance, an adequate gold standard, and head-to-head comparison of FDG-PET and clinical diagnosis, and only 58 entered detailed assessment. Only two studies assessed the accuracy of the comparator (clinical diagnosis) versus any kind of gold-/reference-standard. As to the index-test (FDG-PET-based diagnosis), an independent gold-standard was available in 24% of the examined papers; 38% used an acceptable reference-standard (clinical follow-up); and 38% compared FDG-PET-based diagnosis only to baseline clinical diagnosis. These methodological limitations did not allow for deriving recommendations from evidence. DISCUSSION: An incremental diagnostic value of FDG-PET versus clinical diagnosis or lack thereof cannot be derived from the current literature. Many of the observed limitations may easily be overcome, and we outlined them as research priorities to improve the quality of current evidence. Such improvement is necessary to outline evidence-based guidelines. The available data were anyway provided to expert clinicians who defined interim recommendations.

Indexed as

Positron-Emission TomographyDementiaFluorodeoxyglucose F18HumansSensitivity and SpecificityFluorodeoxyglucose F1818F-FDG PETAlzheimerBiomarkerDementiaDiagnosisEvidence assessmentFDG-PETFluorodeoxyglucose metabolismPositron emission tomographyQuality of evidenceRecommendationsValidation

Identifiers

PMID29713763
OpenAlexW2799799206

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.