Evidence map›Paper›PMID 42530329›Full record

ArticleHuman brain mapping2026

Methodological Choices Strongly Modulate the Sensitivity and Specificity of Lesion-Symptom Mapping Analyses.

Margaret Jane Moore, Chris Rorden, Gail A Robinson, Jason B Mattingley, Nele Demeyere

Abstract read
In one paragraph

Article in Human brain mapping, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Margaret Jane MooreQueensland Brain Institute, University of Queensland, St. Lucia, Queensland, Australia.ORCID https://orcid.org/0000-0001-6914-5978
Chris RordenDepartment of Psychology, University of South Carolina, Colombia, South Carolina, USA.ORCID https://orcid.org/0000-0002-7554-6142
Gail A RobinsonQueensland Brain Institute, University of Queensland, St. Lucia, Queensland, Australia.ORCID https://orcid.org/0000-0002-0078-0364
Jason B MattingleyQueensland Brain Institute, University of Queensland, St. Lucia, Queensland, Australia.ORCID https://orcid.org/0000-0003-0929-9216
Nele DemeyereNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.ORCID https://orcid.org/0000-0003-0416-5147

Funding

Australian Research Council DE240100327Brazil Family FoundationNational Institute for Health Research (NIHR) NIHR302224
6 · The paper itself

Abstract

Lesion-symptom mapping results can vary substantially as a function of specific analysis parameters, but the extent to which individual methodological choices interact to modulate the sensitivity and specificity of results is not clear. Here, we employed a large-scale simulation approach to inform practical recommendations for lesion-symptom mapping studies. Routine clinical imaging from 959 stroke survivors (mean age = 72.5, 49.3% female) was used to conduct 384,780 lesion-symptom mapping analyses based on simulated behavioural data. Each simulated analysis used different combinations of plausible sample inclusion criteria, analysis parameters (e.g., correction factors), analysis types (e.g., univariate vs. multivariate), and underlying target correlates. Simulated analysis accuracy (percent coverage of target correlates, Dice similarity coefficient, and false positives) was compared across designs. Overall, analysis accuracy varied widely and was substantially modulated by the specific design used. Analyses that maximised lesion coverage by including large and diverse samples reliably outperformed analyses using more restricted samples. Analyses using direct total lesion volume controls outperformed analyses using other (or no) volume corrections across all accuracy measures. False discovery rate corrections yielded the best performance in terms of target coverage, while permutation corrections yielded the best Dice coefficients. While multivariate approaches were more accurate than univariate analyses in terms of Dice coefficient, univariate analyses generated higher target hit rates and percent target coverage. These results identify specific analysis designs suitable for studies aiming to maximise their sensitivity and/or specificity to underlying critical correlates, while highlighting the inferential strengths and weaknesses of these complementary approaches.

Indexed as

BrainBrain MappingStrokeAgedAged, 80 and overComputer SimulationFemaleHumansMagnetic Resonance ImagingMaleSensitivity and Specificitylesion‐symptom mappingmultivariate lesion mappingmultiverse analysisneuroimagingstroke

Identifiers

PMID42530329
PMCPMC13421372

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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.