Evidence map›Paper›PMID 37306089›Full record

ArticleHuman brain mapping2023

Network anatomy in logopenic variant of primary progressive aphasia.

Maria Luisa Mandelli, Diego L Lorca-Puls, Sladjana Lukic, Maxime Montembeault, Andrea Gajardo-Vidal, Abigail Licata, Aaron Scheffler, Giovanni Battistella, Stephanie M Grasso, Rian Bogley and 10 more

Open access · goldAbstract read
In one paragraph

Article in Human brain mapping, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Cognitive and brain reserve in bilingual speakers with clinical AD variants.medRxiv : the preprint server for health sciences · 2026
    Article
  6. Non-fluent agrammatic variant of primary progressive aphasia in a bilingual Mandarin/English speaker: a case report.Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists · 2026
    Article
  7. Review
  8. The Diagnostic Role of FDG-PET in Dementias Presenting with Language and Behavioral Symptom.Turk psikiyatri dergisi = Turkish journal of psychiatry · 2026
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 6 institutions in 3 countries.

Maria Luisa MandelliMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.ORCID 0000-0002-2518-2520
Diego L Lorca-PulsMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Sladjana LukicMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Maxime MontembeaultMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Andrea Gajardo-VidalMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Abigail LicataMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Aaron SchefflerDepartment of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
Giovanni BattistellaMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Stephanie M GrassoDepartment of Speech, Language, and Hearing Sciences, University of Texas, Austin, Texas, USA.
Rian BogleyMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Buddhika M RatnasiriMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Renaud La JoieMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Nidhi S MundadaMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Eduardo EuropaDepartment of Communicative Disorders and Sciences, San Jose State University, San Jose, California, USA.
Gil RabinoviciMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Bruce L MillerMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Jessica De LeonMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Maya L HenryDepartment of Speech, Language, and Hearing Sciences, University of Texas, Austin, Texas, USA.
Zachary MillerMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
Maria Luisa Gorno-TempiniMemory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
University of California, San Francisco · USLanguage Computer (United States) · USMassachusetts Eye and Ear Infirmary · USSan Jose State University · USUniversidad del Desarrollo · CLUniversity of Concepción · CL

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Merrilees · 2002 to 2026
$67.2M
Research Education ComponentP30AG062422 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Gil Dan Rabinovici · 2019 to 2026
$36.9M
Progressive Aphasia Cognition Anatomy and ProgressionR01NS050915 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARIA LUISA GORNO TEMPINI · 2004 to 2026
$11.0M
Primary Progressive Aphasia: Cognition, Anatomy and ProgressionRF1NS050915 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GORNO TEMPINI, MARIA LUISA · 2022 to 2022
$4.7M
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
Primary Progressive Aphasia: Beyond the Clinical VariantsK23DC018021 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DELEON, JESSICA ANNE · 2020 to 2024
$995k
Connectome-based spread of neurodegenerative processes in Alzheimer's diseaseK99AG065501 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LA JOIE, RENAUD CHARLES · 2020 to 2021
$253k
Fyn modulation of APP processingR03AG030060 · NIA · GEORGETOWN UNIVERSITY · PI REBECK, G WILLIAM · 2008 to 2009
$130k
NIA NIH HHS K99 AG065501NIA NIH HHS P01 AG019724NIA NIH HHS P30 AG062422NIA NIH HHS R03 AG030060NIDCD NIH HHS K23 DC018021NIDCD NIH HHS K24 DC015544NIDCD NIH HHS R01 DC016291NINDS NIH HHS R01 NS050915NINDS NIH HHS RF1 NS050915
6 · The paper itself

Abstract

The logopenic variant of primary progressive aphasia (lvPPA) is a neurodegenerative syndrome characterized linguistically by gradual loss of repetition and naming skills resulting from left posterior temporal and inferior parietal atrophy. Here, we sought to identify which specific cortical loci are initially targeted by the disease (epicenters) and investigate whether atrophy spreads through predetermined networks. First, we used cross-sectional structural MRI data from individuals with lvPPA to define putative disease epicenters using a surface-based approach paired with an anatomically fine-grained parcellation of the cortical surface (i.e., HCP-MMP1.0 atlas). Second, we combined cross-sectional functional MRI data from healthy controls and longitudinal structural MRI data from individuals with lvPPA to derive the epicenter-seeded resting-state networks most relevant to lvPPA symptomatology and ascertain whether functional connectivity in these networks predicts longitudinal atrophy spread in lvPPA. Our results show that two partially distinct brain networks anchored to the left anterior angular and posterior superior temporal gyri epicenters were preferentially associated with sentence repetition and naming skills in lvPPA. Critically, the strength of connectivity within these two networks in the neurologically-intact brain significantly predicted longitudinal atrophy progression in lvPPA. Taken together, our findings indicate that atrophy progression in lvPPA, starting from inferior parietal and temporoparietal junction regions, predominantly follows at least two partially nonoverlapping pathways, which may influence the heterogeneity in clinical presentation and prognosis.

Indexed as

Alzheimer DiseaseAphasia, Primary ProgressiveAtrophyBrainCross-Sectional StudiesHumansNeuropsychological TestsAlzheimer's diseasecortical atrophyintrinsic connectivity networkslogopenic variantlongitudinal studyprimary progressive aphasia

Identifiers

PMID37306089
PMCPMC10318204
OpenAlexW4380290683

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.