Evidence map›Paper›PMID 41032666›Full record

ArticleBrain : a journal of neurology2026

Atrophy progression in frontotemporal lobar degeneration-TDP-C with primary progressive aphasia.

Elena Barbieri, Allegra S Kawles, Michelle Los, Jordan Behn, Changiz Geula, Tamar Gefen, Sandra Weintraub, Marek-Marsel Mesulam

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Neuropathology-specific language features in primary progressive aphasia.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  2. Identifying neuropathologic disease in primary progressive aphasia using narrative speech.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  3. Article
  4. 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

8 authors.

Elena BarbieriMesulam Institute for Cognitive Neurology and Alzheimer's Disease, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.ORCID 0000-0002-7303-846X
Allegra S KawlesMesulam Institute for Cognitive Neurology and Alzheimer's Disease, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.ORCID 0000-0003-3153-5350
Michelle LosMesulam Institute for Cognitive Neurology and Alzheimer's Disease, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Jordan BehnMesulam Institute for Cognitive Neurology and Alzheimer's Disease, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Changiz GeulaMesulam Institute for Cognitive Neurology and Alzheimer's Disease, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Tamar GefenMesulam Institute for Cognitive Neurology and Alzheimer's Disease, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Sandra WeintraubMesulam Institute for Cognitive Neurology and Alzheimer's Disease, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.ORCID 0000-0003-2605-5205
Marek-Marsel MesulamMesulam Institute for Cognitive Neurology and Alzheimer's Disease, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.ORCID 0000-0001-5731-851X

Funding

Neuropathology CoreP30AG013854 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI RADEMAKER, ALFRED W. · 1996 to 2020
$28.9M
Research Education Core FP30AG072977 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ROBERT J VASSAR · 2021 to 2026
$26.3M
ASYMMETRIC NEURODEGENERATION AND LANGUAGE IN PRIMARY PROGRESSIVE APHASIAR01AG077444 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MAREK-MARSEL M MESULAM, EMILY J ROGALSKI · 2022 to 2026
$10.4M
PREDOCTORAL AND POSTDOCTORAL TRAINING PROGRAM IN AGING AND DEMENTIAT32AG020506 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ROBERT J VASSAR, SANDRA WEINTRAUB · 2002 to 2026
$9.9M
Anatomic, Pathologic, and Molecular Signatures of FTLD-TDP type CR01AG091388 · NIA · NORTHWESTERN UNIVERSITY · PI CHANGIZ GEULA, Tamar D Gefen · 2025 to 2026
$1.6M
Clinical, Anatomic, and Pathologic Spread of Semantic Language Impairment in the Type C Variant of Frontotemporal Lobar Degeneration due to TDP-43 (TDP-C)F31AG094137 · NIA · NORTHWESTERN UNIVERSITY · PI KAWLES, ALLEGRA · 2025 to 2025
$50k
NIA NIH HHS DGE-1842165NIA NIH HHS F31 AG094137NIA NIH HHS F31AG094137NIA NIH HHS P30 AG013854NIA NIH HHS P30AG013854NIA NIH HHS P30 AG072977NIA NIH HHS P30AG072977NIA NIH HHS R01 AG077444NIA NIH HHS R01AG077444NIA NIH HHS R01 AG091388NIA NIH HHS R01AG091388NIA NIH HHS T32 AG020506NIA NIH HHS T32AG020506
6 · The paper itself

Abstract

Clinicopathological correlations in neurodegenerative diseases have led to new insights on the neurobiology of selective vulnerability and the anatomy of cognitive networks. The neuropathological entity of frontotemporal lobar degeneration with abnormal precipitates of the transactive response DNA binding protein TDP-43 (FTLD-TDP) of type C (TDP-C) is one of the most distinctive examples. TDP-C invariably starts with neurodegeneration (atrophy) confined to the temporopolar regions. The process is usually asymmetric, causing behavioural abnormalities and associative agnosia when predominantly right-sided, semantic primary progressive aphasia when left-sided, and semantic dementia when bilateral. In this study, we investigated the relationship between progression of atrophy and the progressive dissolution of word comprehension in TDP-C patients with asymmetric left temporopolar region degeneration. For the sake of homogeneity and in order to use a common yardstick of functional progression, we focused on patients with leftward asymmetry and initially isolated verbal impairment. Using data from 24 visits with structural MRI scans and specialized tests of naming, word definition and word-to-picture matching, we stratified the anatomy of peak degeneration sites according to three increasingly advanced stages of impaired noun representations. According to this pattern of progression, an initial stage of relatively isolated anomia is followed by additional intra-category blurring of word meaning and, at still more advanced stages, inter-category blurring. Voxel-based morphometry maps of grey matter volume were binarized to identify regions most frequently atrophied at each of these stages. The results illustrate that the progressive dissolution of word meaning is associated with caudal progression of atrophy from the left temporopolar cortex at initial stages to more posterior fusiform, lateral temporal and temporo-occipital regions in later stages. The stratification of progressive atrophy by precisely characterized stages of word comprehension impairment, rather than by estimated time of symptom onset, offers a functional rather than only chronological anatomy of progression for TDP-C and a clearer view of the relationship between temporopolar region components and the cognitive mapping of word representations.

Indexed as

Aphasia, Primary ProgressiveFrontotemporal Lobar DegenerationAgedAtrophyDisease ProgressionDNA-Binding ProteinsFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNeuropsychological TestsTemporal LobeDNA-Binding Proteinsatrophyconceptual knowledgefrontotemporal lobar degenerationprimary progressive aphasiatemporal lobe

Identifiers

PMID41032666
PMCPMC12717277

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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.