Evidence map›Paper›PMID 34535718›Full record

ArticleScientific reports2021

Lesion site and therapy time predict responses to a therapy for anomia after stroke: a prognostic model development study.

Thomas M H Hope, Davide Nardo, Rachel Holland, Sasha Ondobaka, Haya Akkad, Cathy J Price, Alexander P Leff, Jenny Crinion

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. 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
0.7field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Gene Expression-Based Lesion-Symptom Mapping:The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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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

8 authors at 3 institutions in 1 country.

Thomas M H HopeInstitute of Cognitive Neuroscience, University College London, 17-19 Queen Square, London, WC1N 3AR, UK. t.hope@ucl.ac.uk.
Davide NardoInstitute of Cognitive Neuroscience, University College London, 17-19 Queen Square, London, WC1N 3AR, UK.
Rachel HollandDivision of Language and Communication Science, City University of London, London, UK.
Sasha OndobakaInstitute of Cognitive Neuroscience, University College London, 17-19 Queen Square, London, WC1N 3AR, UK.
Haya AkkadInstitute of Cognitive Neuroscience, University College London, 17-19 Queen Square, London, WC1N 3AR, UK.
Cathy J PriceWellcome Centre for Human Neuroimaging, University College London, London, UK.
Alexander P LeffInstitute of Cognitive Neuroscience, University College London, 17-19 Queen Square, London, WC1N 3AR, UK.
Jenny CrinionInstitute of Cognitive Neuroscience, University College London, 17-19 Queen Square, London, WC1N 3AR, UK.
University College London · GBNational Hospital for Neurology and Neurosurgery · GBCity, University of London · GB

Funding

Medical Research Council G0701888Medical Research Council MC_UU_00005/1Medical Research Council MR/M023672/1Wellcome Trust 106161/Z/14/ZWellcome Trust 203147/Z/16/ZWellcome Trust 205103/Z/16/Z
6 · The paper itself

Abstract

Stroke is a leading cause of disability, and language impairments (aphasia) after stroke are both common and particularly feared. Most stroke survivors with aphasia exhibit anomia (difficulties with naming common objects), but while many therapeutic interventions for anomia have been proposed, treatment effects are typically much larger in some patients than others. Here, we asked whether that variation might be more systematic, and even predictable, than previously thought. 18 patients, each at least 6 months after left hemisphere stroke, engaged in a computerised treatment for their anomia over a 6-week period. Using only: (a) the patients' initial accuracy when naming (to-be) trained items; (b) the hours of therapy that they devoted to the therapy; and (c) whole-brain lesion location data, derived from structural MRI; we developed Partial Least Squares regression models to predict the patients' improvements on treated items, and tested them in cross-validation. Somewhat surprisingly, the best model included only lesion location data and the hours of therapy undertaken. In cross-validation, this model significantly out-performed the null model, in which the prediction for each patient was simply the mean treatment effect of the group. This model also made promisingly accurate predictions in absolute terms: the correlation between empirical and predicted treatment response was 0.62 (95% CI 0.27, 0.95). Our results indicate that individuals' variation in response to anomia treatment are, at least somewhat, systematic and predictable, from the interaction between where and how much lesion damage they have suffered, and the time they devoted to the therapy.

Indexed as

AnomiaBrainDisease ManagementFemaleHumansMalePrognosisStroke

Identifiers

PMID34535718
PMCPMC8448867
OpenAlexW3200571259

What OpenQuestion holds

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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.