Evidence map›Paper›PMID 40726747›Full record

ArticleJournal of healthcare informatics research2025

Behavioral Clusters and Lesion Distributions in Ischemic Stroke, Based on NIHSS Similarity Network.

Louis Fabrice Tshimanga, Andrea Zanola, Silvia Facchini, Antonio Luigi Bisogno, Lorenzo Pini, Manfredo Atzori, Maurizio Corbetta

Abstract read
In one paragraph

Article in Journal of healthcare informatics research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Louis Fabrice Tshimanga *Department of Neuroscience, University of Padua, Padua, 35128 Italy.ORCID https://orcid.org/0009-0002-1240-4830
Andrea Zanola *Department of Neuroscience, University of Padua, Padua, 35128 Italy.ORCID https://orcid.org/0000-0001-6973-8634
Silvia FacchiniDepartment of Neuroscience, University of Padua, Padua, 35128 Italy.
Antonio Luigi BisognoDepartment of Neuroscience, University of Padua, Padua, 35128 Italy.
Lorenzo PiniPadova Neuroscience Center, University of Padua, Padua, 35128 Italy.
Manfredo AtzoriDepartment of Neuroscience, University of Padua, Padua, 35128 Italy.
Maurizio CorbettaDepartment of Neuroscience, University of Padua, Padua, 35128 Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stroke, a leading cause of mortality and disability, results in diverse dysfunctions linked to brain lesion locations. The intricate relationship between lesions and symptoms often defies linear analysis methods. Unraveling these connections can yield valuable insights to enhance patient care, optimize rehabilitation strategies, and unveil fundamental principles of healthy brain function. This study introduces a novel unsupervised framework to stratify patients into clinically coherent subgroups based on behavioral symptom profiles and identify their distinct neural correlates. NIHSS assessments are modeled as ordinal feature vectors, integrating symptom prevalence, severity, and covariance patterns into a unified measure of behavioral similarity among stroke survivors. The resulting similarity network is partitioned using Repeated Spectral Clustering, which accumulates partition evidence for stable subgroup discovery. Voxel-wise lesion analysis subsequently highlights each subgroup's collective neuroanatomical signatures. Despite being identified in a completely unsupervised manner based solely on NIHSS scores, the emergent clusters correspond to well-documented syndromes, validating the purely data-driven symptom groupings alongside established neurological knowledge. Clusters exhibit critical voxels in group-specific anatomical locations, even when average lesion maps spatially overlap, suggesting that our method disentangles functionally distinct substrates within shared vascular territories. Our workflow represents a significant methodological advancement, providing robust, clinically relevant insights into symptom phenotyping and lesion patterns. The framework's mathematical transparency and validation against canonical knowledge underscore its potential for generalization to multimodal biomarkers and broader biomedical research. To foster reproducibility, we provide open-source code.

Indexed as

ClusteringMachine learningNIHSSStroke

Identifiers

PMID40726747
PMCPMC12290165

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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.