Evidence map›Paper›PMID 34353857›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2022

Comparison of clinical rating scales in genetic frontotemporal dementia within the GENFI cohort.

Georgia Peakman, Lucy L Russell, Rhian S Convery, Jennifer M Nicholas, John C Van Swieten, Lize C Jiskoot, Fermin Moreno, Raquel Sanchez-Valle, Robert Laforce, Caroline Graff and 22 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of neurology, neurosurgery, and psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. The role of bilingualism on functional decline and neurodegeneration in distinct ADRD clinical syndromes.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Preparing for the age of therapeutic trials in frontotemporal lobar degeneration.Journal of neurology, neurosurgery, and psychiatry · 2022
    Article
  10. 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

32 authors at 20 institutions in 10 countries.

Georgia PeakmanDepartment of Neurodegenerative Disease, University College London Dementia Research Centre, London, UK.ORCID 0000-0002-3319-138X
Lucy L RussellDepartment of Neurodegenerative Disease, University College London Dementia Research Centre, London, UK.
Rhian S ConveryDepartment of Neurodegenerative Disease, University College London Dementia Research Centre, London, UK.ORCID 0000-0002-9477-1812
Jennifer M NicholasDepartment of Medical Statistics, London School of Hygiene & Tropical Medicine, London, UK.
John C Van SwietenDepartment of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.ORCID 0000-0001-6278-6844
Lize C JiskootDepartment of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-1120-1858
Fermin MorenoCognitive Disorders Unit, Department of Neurology, Hospital Universitario de Donostia, San Sebastian, Spain.
Raquel Sanchez-ValleAlzheimer's Disease and Other Cognitive Disorders Unit, Neurology Service, Hospital Clínic, Institut d'Investigacións Biomèdiques August Pi I Sunyer, University of Barcelona, Barcelona, Spain.
Robert LaforceClinique Interdisciplinaire de Mémoire, Département des Sciences Neurologiques, CHU de Québec, and Faculté de Médecine, Laval University, Quebec, Quebec, Canada.
Caroline GraffCenter for Alzheimer Research, Division of Neurogeriatrics, Department of Neurobiology, Care Sciences and Society, Bioclinicum, Karolinska Institutet, Stockholm, Sweden.
Mario MasellisSunnybrook Health Sciences Centre, Sunnybrook Research Institute, University of Toronto, Toronto, Ontario, Canada.
Maria Carmela TartagliaTanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada.
James B RoweDepartment of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0001-7216-8679
Barbara BorroniNeurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.ORCID 0000-0001-9340-9814
Elizabeth FingerClinical Neurological Sciences, University of Western Ontario, London, Ontario, Canada.ORCID 0000-0003-4461-7427
Matthis SynofzikDept. of Neurodegenerative Diseases, Eberhard Karls University Tubingen Hertie Institute for Clinical Brain Research, Tubingen, Germany.
Daniela GalimbertiFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.ORCID 0000-0002-9284-5953
Rik VandenbergheLaboratory for Cognitive Neurology, Department of Neurosciences, KU Leuven, Leuven, Belgium.
Alexandre de MendonçaFaculty of Medicine, University of Lisbon, Lisbon, Portugal.
Chris R ButlerNuffield Department of Clinical Neurosciences, University of Oxford Medical Sciences Division, Oxford, UK.
Alex GerhardDivision of Neuroscience and Experimental Psychology, Wolfson Molecular Imaging Centre, The University of Manchester, Manchester, UK.ORCID 0000-0002-8071-6062
Simon DucharmeDepartment of Psychiatry, McGill University Health Centre, Montreal, Québec, Canada.ORCID 0000-0002-7309-1113
Isabelle Le BerSorbonne Université, Paris Brain Institute - Institut du Cerveau - ICM, Inserm U1127, CNRS UMR 7225, Hôpital Universitaire Pitié Salpêtrière, Paris, France.ORCID 0000-0002-2508-5181
Fabrizio TagliaviniFondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.
Isabel SantanaUniversity Hospital of Coimbra (HUC), Neurology Service, University of Coimbra Faculty of Medicine, Coimbra, Portugal.
Florence PasquierUniversity of Lille, Lille, France.
Johannes LevinDepartment of Neurology, Ludwig-Maximilians-Universität München, Munchen, Germany.
Adrian DanekDepartment of Neurology, Ludwig-Maximilians-Universität München, Munchen, Germany.ORCID 0000-0001-8857-5383
Markus OttoDepartment of Neurology, University of Ulm, Ulm, Germany.ORCID 0000-0002-6647-5944
Sandro SorbiDepartment of Neurofarba, University of Florence, Firenze, Italy.ORCID 0000-0002-0380-6670
Jonathan D RohrerDepartment of Neurodegenerative Disease, University College London Dementia Research Centre, London, UK j.rohrer@ucl.ac.uk.ORCID 0000-0002-6155-8417
Genetic FTD Initiative (GENFI)
UK Dementia Research Institute · GBErasmus MC · NLGerman Center for Neurodegenerative Diseases · DEBiogipuzkoa Health Research Institute · ESCentre National de la Recherche Scientifique · FRDon Carlo Gnocchi Foundation · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITInserm · FRKarolinska University Hospital · SELondon School of Hygiene & Tropical Medicine · GBLudwig-Maximilians-Universität München · DEMontreal Neurological Institute and Hospital · CASunnybrook Health Science Centre · CAUniversitat de Barcelona · ESUniversität Ulm · DEUniversité Laval · CAUniversity of Brescia · ITUniversity of Cambridge · GBUniversity of Coimbra · PTUniversity of Lisbon · PT

Funding

NATIONAL ALZHEIMERS COORDINATING CENTER (NACC)U01AG016976 · NIA · UNIVERSITY OF WASHINGTON · PI KUKULL, WALTER ANTHONY · 1999 to 2020
$72.8M
National Alzheimer's Coordinating CenterU24AG072122 · NIA · UNIVERSITY OF WASHINGTON · PI STEPHENS, KARI A · 2021 to 2025
$45.8M
Medical Research Council MC_UU_00024/1Medical Research Council MR/J009482/1Medical Research Council MR/M008525/1Medical Research Council MR/M023664/1Medical Research Council MR/T046015/1NIA NIH HHS U01 AG016976NIA NIH HHS U24 AG072122
6 · The paper itself

Abstract

backgroundTherapeutic trials are now underway in genetic forms of frontotemporal dementia (FTD) but clinical outcome measures are limited. The two most commonly used measures, the Clinical Dementia Rating (CDR)+National Alzheimer's Disease Coordinating Center (NACC) Frontotemporal Lobar Degeneration (FTLD) and the FTD Rating Scale (FRS), have yet to be compared in detail in the genetic forms of FTD.

methodsThe CDR+NACC FTLD and FRS were assessed cross-sectionally in 725 consecutively recruited participants from the Genetic FTD Initiative: 457 mutation carriers (77 microtubule-associated protein tau (

resultsCross-sectionally, the mean FRS score was lower in all genetic groups compared with controls:

conclusionsBoth the FRS and CDR+NACC FTLD measure disease severity in genetic FTD mutation carriers throughout the timeline of their disease, although the FRS may be preferable as an outcome measure. However, neither address a number of key symptoms in the FTD spectrum, for example, motor and neuropsychiatric deficits, which future scales will need to incorporate.

Indexed as

Mental Status and Dementia TestsC9orf72 ProteinCohort StudiesCross-Sectional StudiesDisease ProgressionFrontotemporal DementiaHumansMutationtau ProteinsC9orf72 ProteinMAPT protein, humantau Proteinsfrontotemporal dementia

Identifiers

PMID34353857
PMCPMC8785074
OpenAlexW3188860209

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.