Evidence map›Paper›PMID 29717332›Full record

ReviewEuropean journal of nuclear medicine and molecular imaging2018

Clinical utility of FDG-PET in amyotrophic lateral sclerosis and Huntington's disease.

Federica Agosta, Daniele Altomare, Cristina Festari, Stefania Orini, Federica Gandolfo, Marina Boccardi, Javier Arbizu, Femke Bouwman, Alexander Drzezga, Peter Nestor and 4 more

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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  6. EANM procedure guidelines for brain PET imaging using [European journal of nuclear medicine and molecular imaging · 2022
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  7. Review
  8. Article
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  13. 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
  14. 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

14 authors at 8 institutions in 8 countries.

Federica AgostaNeuroimaging Research Unit, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy. agosta.federica@hsr.it.ORCID http://orcid.org/0000-0003-3121-4979
Daniele AltomareLANE - Laboratory of Alzheimer's Neuroimaging & Epidemiology, IRCCS S. Giovanni di Dio, Fatebenefratelli, Brescia, Italy.
Cristina FestariLANE - Laboratory of Alzheimer's Neuroimaging & Epidemiology, IRCCS S. Giovanni di Dio, Fatebenefratelli, Brescia, Italy.
Stefania OriniAlzheimer Operative Unit, IRCCS S. Giovanni di Dio, Fatebenefratelli, Brescia, Italy.
Federica GandolfoAlzheimer Operative Unit, IRCCS S. Giovanni di Dio, Fatebenefratelli, Brescia, Italy.
Marina BoccardiLANE - Laboratory of Alzheimer's Neuroimaging & Epidemiology, IRCCS S. Giovanni di Dio, Fatebenefratelli, Brescia, Italy. marina.boccardi@unige.ch.
Javier ArbizuDepartment of Nuclear Medicine, Clinica Universidad de Navarra, University of Navarra, Pamplona, Spain.
Femke BouwmanDepartment of Neurology & Alzheimer Center, Amsterdam Neuroscience, VU University Medical Center, Amsterdam, the Netherlands.
Alexander DrzezgaDepartment of Nuclear Medicine, University Hospital of Cologne, University of Cologne and German Center for Neurodegenerative Diseases (DZNE), Cologne, Germany.
Peter NestorGerman Center for Neurodegenerative Diseases (DZNE), Magdeburg, Germany.
Flavio NobiliDepartment of Neuroscience (DINOGMI), University of Genoa and Polyclinic San Martino Hospital, Genoa, Italy.
Zuzana WalkerDivision of Psychiatry & Essex Partnership University NHS Foundation Trust, University College London, London, UK.
Marco PaganiInstitute of Cognitive Sciences and Technologies, CNR, Rome, Italy.
EANM-EAN Task Force for the Prescription of FDG-PET for Dementing Neurodegenerative Disorders
Centro San Giovanni di Dio Fatebenefratelli · ITSouth Essex Partnership University Foundation NHS Trust · GBThe University of Queensland · AUUniversity of Geneva · CHVita-Salute San Raffaele University · ITAmsterdam Neuroscience · NLKarolinska University Hospital · SEUniversity of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo evaluate the incremental value of FDG-PET over clinical tests in: (i) diagnosis of amyotrophic lateral sclerosis (ALS); (ii) picking early signs of neurodegeneration in patients with a genetic risk of Huntington's disease (HD); and detecting metabolic changes related to cognitive impairment in (iii) ALS and (iv) HD patients.

methodsFour comprehensive literature searches were conducted using the PICO model to extract evidence from relevant studies. An expert panel then voted using the Delphi method on these four diagnostic scenarios.

resultsThe availability of evidence was good for FDG-PET utility to support the diagnosis of ALS, poor for identifying presymptomatic subjects carrying HD mutation who will convert to HD, and lacking for identifying cognitive-related metabolic changes in both ALS and HD. After the Delphi consensual procedure, the panel did not support the clinical use of FDG-PET for any of the four scenarios.

conclusionRelative to other neurodegenerative diseases, the clinical use of FDG-PET in ALS and HD is still in its infancy. Once validated by disease-control studies, FDG-PET might represent a potentially useful biomarker for ALS diagnosis. FDG-PET is presently not justified as a routine investigation to predict conversion to HD, nor to detect evidence of brain dysfunction justifying cognitive decline in ALS and HD.

Indexed as

Positron-Emission TomographyAmyotrophic Lateral SclerosisBrainFluorodeoxyglucose F18HumansHuntington DiseaseRadiopharmaceuticalsFluorodeoxyglucose F18RadiopharmaceuticalsAmyotrophic lateral sclerosisBehavioral abnormalitiesCognitive impairmentFDG-PETHuntington’s diseaseMutation gene carrier

Identifiers

PMID29717332
OpenAlexW2801552310

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.