Evidence map›Paper›PMID 26106560›Full record

ArticleNeuroImage. Clinical2015

Longitudinal gray matter contraction in three variants of primary progressive aphasia: A tenser-based morphometry study.

Simona Maria Brambati, Serena Amici, Caroline A Racine, John Neuhaus, Zachary Miller, Jenny Ogar, Nina Dronkers, Bruce L Miller, Howard Rosen, Maria Luisa Gorno-Tempini

Abstract read
In one paragraph

Article in NeuroImage. Clinical, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
–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

45 citing papers in PubMed.

  1. Article
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  11. Symptom-led staging for primary progressive aphasia.medRxiv : the preprint server for health sciences · 2023
    Article
  12. Observational
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Neuroimaging in Frontotemporal Dementia: Heterogeneity and Relationships with Underlying Neuropathology.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
    Review
  19. Review
  20. 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

10 authors.

Simona Maria BrambatiCentre de Recherche de l'Institut Universitaire de Gériatrie de Montréal, Montréal, QC, Canada.
Serena AmiciDepartment of Neurology, Memory and Aging Center, University of California, San Francisco, San Francisco, CA, USA.
Caroline A RacineDepartment of Neurological Surgery, University of California, San Francisco, San Francisco, CA, USA.
John NeuhausDepartment of Biostatistics, University of California, San Francisco, San Francisco, CA, USA.
Zachary MillerDepartment of Neurology, Memory and Aging Center, University of California, San Francisco, San Francisco, CA, USA.
Jenny OgarDepartment of Neurology, Memory and Aging Center, University of California, San Francisco, San Francisco, CA, USA ; Department of Veteran's Affairs, Martinez, CA, USA ; University of California, Davis, CA, USA.
Nina DronkersDepartment of Neurology, Memory and Aging Center, University of California, San Francisco, San Francisco, CA, USA ; Department of Veteran's Affairs, Martinez, CA, USA ; University of California, Davis, CA, USA.
Bruce L MillerDepartment of Neurology, Memory and Aging Center, University of California, San Francisco, San Francisco, CA, USA.
Howard RosenDepartment of Neurology, Memory and Aging Center, University of California, San Francisco, San Francisco, CA, USA.
Maria Luisa Gorno-TempiniDepartment of Neurology, Memory and Aging Center, University of California, San Francisco, San Francisco, CA, USA.

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Merrilees · 2002 to 2026
$67.2M
ZD1839 FOR MALIGNANT ASTROCYTOMA OR GLIOBLASTOMA AND MENINGIOMAM01RR000079 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KESSLER, DAVID A · 1985 to 2006
$26.0M
Progressive Aphasia Cognition Anatomy and ProgressionR01NS050915 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARIA LUISA GORNO TEMPINI · 2004 to 2026
$11.0M
The Frontotemporal Lobar Degeneration Neuroimaging InitiativeR01AG032306 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSEN, HOWARD J · 2009 to 2013
$10.0M
Genetic Determinants of TauopathiesF31NS084556 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, JASON ANDREW · 2013 to 2015
$80k
NCRR NIH HHS M01 RR000079NCRR NIH HHS M01 RR00079NIA NIH HHS P01 AG019724NIA NIH HHS P50 AG-03-006NIA NIH HHS R01 AG032306NINDS NIH HHS R01 NS050915NINDS NIH HHS R01 NS50915
6 · The paper itself

Abstract

The present study investigated the pattern of longitudinal changes in cognition and anatomy in three variants of primary progressive aphasia (PPA). Eight patients with the non-fluent variant of PPA (nfvPPA), 13 patients with the semantic variant (svPPA), seven patients with the logopenic variant (lvPPA), and 29 age-matched, neurologically healthy controls were included in the study. All participants underwent longitudinal MRI, neuropsychological and language testing at baseline and at a 1-year follow-up. Tenser-based morphometry (TBM) was applied to T1-weighted MRI images in order to map the progression of gray and white matter atrophy over a 1-year period. Results showed that each patient group was characterized by a specific pattern of cognitive and anatomical changes. Specifically, nfvPPA patients showed gray matter atrophy progression in the left frontal and subcortical areas as well as a decline in motor speech and executive functions; svPPA patients presented atrophy progression in the medial and lateral temporal lobe and decline in semantic memory abilities; and lvPPA patients showed atrophy progression in lateral/posterior temporal and medial parietal regions with a decline in memory, sentence repetition and calculations. In addition, in all three variants, the white matter fibers underlying the abovementioned cortical areas underwent significant volume contraction over a 1-year period. Overall, these results indicate that the three PPA variants present distinct patterns of neuroanatomical contraction, which reflect their clinical and cognitive progression.

Indexed as

Disease ProgressionAgedAphasia, Primary ProgressiveAtrophyExecutive FunctionFemaleFollow-Up StudiesGray MatterHumansMagnetic Resonance ImagingMaleMiddle AgedPrimary Progressive Nonfluent Aphasia

Identifiers

PMID26106560
PMCPMC4473099

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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.