Evidence map›Paper›PMID 37038501›Full record

ArticleBrain communications2023

Spared speech fluency is associated with increased functional connectivity in the speech production network in semantic variant primary progressive aphasia.

Maxime Montembeault, Zachary A Miller, Amandine Geraudie, Peter Pressman, Antoine Slegers, Carly Millanski, Abigail Licata, Buddhika Ratnasiri, Maria Luisa Mandelli, Maya Henry and 6 more

Open access · goldAbstract read
In one paragraph

Article in Brain communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Language deficits across PET-based Braak stages of tau accumulation in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
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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

16 authors at 7 institutions in 3 countries.

Maxime MontembeaultMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
Zachary A MillerMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
Amandine GeraudieMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
Peter PressmanDepartment of Neurology, Behavioral Neurology Section, University of Colorado Anschutz Medical Campus, Aurora, CO 80238, USA.
Antoine SlegersDépartement de Psychologie, Université de Montréal, Montréal, QC H3C 3J7, Canada.
Carly MillanskiMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
Abigail LicataMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
Buddhika RatnasiriMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
Maria Luisa MandelliMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
Maya HenryDepartment of Speech, Language, and Hearing Sciences, The University of Texas at Austin, Austin, TX 78712-0114, USA.
Yann CobigoMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
Howard J RosenMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
Bruce L MillerMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
Simona M BrambatiDépartement de Psychologie, Université de Montréal, Montréal, QC H3C 3J7, Canada.
Maria Luisa Gorno-TempiniMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
Giovanni BattistellaMemory and Aging Center, Department of Neurology, University of California in San Francisco, San Francisco, CA 94158, USA.
University Memory and Aging Center · USInstitut Universitaire de Gériatrie de Montréal · CADouglas Mental Health University Institute · CAMassachusetts Eye and Ear Infirmary · USThe University of Texas at Austin · USUniversité Fédérale de Toulouse Midi-Pyrénées · FRUniversity of Colorado Anschutz Medical Campus · US

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Merrilees · 2002 to 2026
$67.2M
PrPSc SPECIFIC INTERACTION WITH NOVEL PrP-Fc FUSION PROTEINSP50AG023501 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MILLER, BRUCE L · 2004 to 2018
$27.1M
The Four Repeat Tauopathy Neuroimaging InitiativeR01AG038791 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BOXER, ADAM L. · 2010 to 2020
$18.1M
Progressive Aphasia Cognition Anatomy and ProgressionR01NS050915 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARIA LUISA GORNO TEMPINI · 2004 to 2026
$11.0M
Training - The Frontotemporal Lobar Degeneration Clinical Research ConsortiumU54NS092089 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BOXER, ADAM L. · 2014 to 2018
$6.4M
Primary Progressive Aphasia: Cognition, Anatomy and ProgressionRF1NS050915 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GORNO TEMPINI, MARIA LUISA · 2022 to 2022
$4.7M
Measuring Altered Social Behavior in Neurodegenerative DiseaseR01AG029577 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RANKIN, KATHERINE P · 2008 to 2018
$3.6M
Establishing Evidence-based Treatment for Speech and Language in Primary Progressive AphasiaR01DC016291 · NIDCD · UNIVERSITY OF TEXAS AT AUSTIN · PI HENRY, MAYA · 2017 to 2021
$3.3M
Training program in the neurology of language and neurodegenerative aphasiasK24DC015544 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GORNO TEMPINI, MARIA LUISA · 2016 to 2025
$1.9M
Multimodal Imaging in Frontotemporal DegenerationK24AG045333 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSEN, HOWARD J · 2013 to 2023
$1.9M
Neuropathological basis of brain network dysfunctionK08AG052648 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SPINA, SALVATORE · 2016 to 2020
$852k
NIA NIH HHS K08 AG052648NIA NIH HHS K24 AG045333NIA NIH HHS P01 AG019724NIA NIH HHS P50 AG023501NIA NIH HHS R01 AG029577NIA NIH HHS R01 AG038791NIDCD NIH HHS K24 DC015544NIDCD NIH HHS R01 DC016291NINDS NIH HHS R01 NS050915NINDS NIH HHS RF1 NS050915NINDS NIH HHS U54 NS092089
6 · The paper itself

Abstract

Semantic variant primary progressive aphasia is a clinical syndrome characterized by marked semantic deficits, anterior temporal lobe atrophy and reduced connectivity within a distributed set of regions belonging to the functional network associated with semantic processing. However, to fully depict the clinical signature of semantic variant primary progressive aphasia, it is necessary to also characterize preserved neural networks and linguistic abilities, such as those subserving speech production. In this case-control observational study, we employed whole-brain seed-based connectivity on task-free MRI data of 32 semantic variant primary progressive aphasia patients and 46 healthy controls to investigate the functional connectivity of the speech production network and its relationship with the underlying grey matter. We investigated brain-behaviour correlations with speech fluency measures collected through clinical tests (verbal agility) and connected speech (speech rate and articulation rate). As a control network, we also investigated functional connectivity within the affected semantic network. Patients presented with increased connectivity in the speech production network between left inferior frontal and supramarginal regions, independent of underlying grey matter volume. In semantic variant primary progressive aphasia patients, preserved (verbal agility) and increased (articulation rate) speech fluency measures correlated with increased connectivity between inferior frontal and supramarginal regions. As expected, patients demonstrated decreased functional connectivity in the semantic network (dependent on the underlying grey matter atrophy) associated with average nouns' age of acquisition during connected speech. Collectively, these results provide a compelling model for studying compensation mechanisms in response to disease that might inform the design of future rehabilitation strategies in semantic variant primary progressive aphasia.

Indexed as

compensation mechanismfunctional connectivitysemanticssemantic variant of primary progressive aphasiaspeech production

Identifiers

PMID37038501
PMCPMC10082556
OpenAlexW4327553794

What Socratic holds

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LicenceCC BY
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 Socratic graph.