Evidence map›Paper›PMID 30847466›Full record

ArticleBrain : a journal of neurology2019

Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study.

Henri J M M Mutsaerts, Saira S Mirza, Jan Petr, David L Thomas, David M Cash, Martina Bocchetta, Enrico de Vita, Arron W S Metcalfe, Zahra Shirzadi, Andrew D Robertson and 22 more

Erratum issuedAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 31 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 3 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

31 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Gray matter hypoperfusion is a late pathological event in the course of Alzheimer's disease.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

32 authors.

Henri J M M MutsaertsHurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
Saira S MirzaHurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
Jan PetrPET Center, Institute of Radiopharmaceutical Cancer Research, Helmholtz-Zentrum Dresden-Rossendorf, Dresden, Germany.
David L ThomasInstitute of Neurology, University College London, London, UK.
David M CashInstitute of Neurology, University College London, London, UK.
Martina BocchettaInstitute of Neurology, University College London, London, UK.
Enrico de VitaInstitute of Neurology, University College London, London, UK.
Arron W S MetcalfeHurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
Zahra ShirzadiHurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
Andrew D RobertsonHurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
Maria Carmela TartagliaTanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Canada.
Sara B MitchellHurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
Sandra E BlackHurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
Morris FreedmanDivision of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada.
David Tang-WaiMemory Clinic, University Health Network, Toronto, Canada.
Ron KerenMemory Clinic, University Health Network, Toronto, Canada.
Ekaterina RogaevaTanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Canada.
John van SwietenDepartment of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.
Robert LaforceClinique Interdisciplinaire de Mémoire (CIME), Département des Sciences Neurologiques, CHU de Québec, Faculté de médecine, Université Laval, Québec, Canada.
Fabrizio TagliaviniFondazione Istituto di Ricovero e Cura a Carattere Scientifico, Milan, Italy.
Barbara BorroniDepartment of Medical and Experimental Sciences, University of Brescia, Brescia, Italy.
Daniela GalimbertiCentro Dino Ferrari, Fondazione Ca' Granda IRCCS Ospedale Policlinico, University of Milan, Milan, Italy.
James B RoweDepartment of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Caroline GraffDepartment of Geriatric Medicine, Karolinska Institutet, Stockholm, Sweden.
Giovanni B FrisoniIRCCS San Giovanni di Dio Fatebenefratelli, Brescia, Italy.
Elizabeth FingerDepartment of Clinical Neurological Sciences, University of Western Ontario, London, Canada.
Sandro SorbiDepartment of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy.
Alexandre de MendonçaNeurology Department, Faculty of Medicine of Lisbon, Portugal.
Jonathan D RohrerInstitute of Neurology, University College London, London, UK.
Bradley J MacIntoshHurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
Mario MasellisHurvitz Brain Sciences Program, Sunnybrook Research Institute, University of Toronto, Toronto, Canada.
GENetic Frontotemporal dementia Initiative (GENFI)

Funding

CIHR MOP 327387Medical Research Council MC_U123160651Medical Research Council MC_UU_00024/1Medical Research Council MR/J009482/1Medical Research Council MR/M008525/1Medical Research Council MR/M009041/1Medical Research Council MR/M023664/1Medical Research Council MR/M024873/1
6 · The paper itself

Abstract

Genetic forms of frontotemporal dementia are most commonly due to mutations in three genes, C9orf72, GRN or MAPT, with presymptomatic carriers from families representing those at risk. While cerebral blood flow shows differences between frontotemporal dementia and other forms of dementia, there is limited evidence of its utility in presymptomatic stages of frontotemporal dementia. This study aimed to delineate the cerebral blood flow signature of presymptomatic, genetic frontotemporal dementia using a voxel-based approach. In the multicentre GENetic Frontotemporal dementia Initiative (GENFI) study, we investigated cross-sectional differences in arterial spin labelling MRI-based cerebral blood flow between presymptomatic C9orf72, GRN or MAPT mutation carriers (n = 107) and non-carriers (n = 113), using general linear mixed-effects models and voxel-based analyses. Cerebral blood flow within regions of interest derived from this model was then explored to identify differences between individual gene carrier groups and to estimate a timeframe for the expression of these differences. The voxel-based analysis revealed a significant inverse association between cerebral blood flow and the expected age of symptom onset in carriers, but not non-carriers. Regions included the bilateral insulae/orbitofrontal cortices, anterior cingulate/paracingulate gyri, and inferior parietal cortices, as well as the left middle temporal gyrus. For all bilateral regions, associations were greater on the right side. After correction for partial volume effects in a region of interest analysis, the results were found to be largely driven by the C9orf72 genetic subgroup. These cerebral blood flow differences first appeared approximately 12.5 years before the expected symptom onset determined on an individual basis. Cerebral blood flow was lower in presymptomatic mutation carriers closer to and beyond their expected age of symptom onset in key frontotemporal dementia signature regions. These results suggest that arterial spin labelling MRI may be a promising non-invasive imaging biomarker for the presymptomatic stages of genetic frontotemporal dementia.

Indexed as

AdultAgedBrainC9orf72 ProteinCerebrovascular CirculationCross-Sectional StudiesFemaleFrontotemporal DementiaHeterozygoteHumansMagnetic Resonance ImagingMaleMiddle AgedMutationNeuropsychological TestsProgranulinsC9orf72 ProteinC9orf72 protein, humanGRN protein, humanMAPT protein, humanProgranulinstau Proteinsarterial spin labellingcerebral blood flowgenetic frontotemporal dementiapresymptomatic biomarker

Identifiers

PMID30847466
PMCPMC6439322

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.