Automatically quantified follow-up imaging biomarkers predict clinical outcomes after acute ischemic stroke
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064173%3A_____%2F25%3A43928327" target="_blank" >RIV/00064173:_____/25:43928327 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11120/25:43928327
Result on the web
<a href="https://doi.org/10.3389/fneur.2025.1483138" target="_blank" >https://doi.org/10.3389/fneur.2025.1483138</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3389/fneur.2025.1483138" target="_blank" >10.3389/fneur.2025.1483138</a>
Alternative languages
Result language
angličtina
Original language name
Automatically quantified follow-up imaging biomarkers predict clinical outcomes after acute ischemic stroke
Original language description
Background: Follow-up infarct volume (FIV) is a proposed surrogate endpoint for proof-of-concept clinical studies in acute ischemic stroke (AIS). This study aimed to provide clinical validation of an automated FIV algorithm, demonstrating the association of imaging biomarkers with clinical outcomes to support the use of these imaging endpoints in clinical trials. Methods: Data were gathered for adult AIS patients undergoing mechanical thrombectomy with follow-up imaging 12-96 h from initial assessment. Non-contrast computed tomography was used to quantify infarct volume. Image processing used the AI-powered software Brainomix 360 Stroke (Brainomix Ltd., Oxford, United Kingdom) and Brainomix core lab research software. Measures included total FIV and components-ischemic injury corrected FIV (cFIV), hemorrhagic transformation (HT), anatomical distortion (AD; a marker of edema) and infarct growth (IG). The primary clinical endpoint was modified Rankin Scale (mRS) at 90 days; secondary clinical endpoint was NIH Stroke Scale (NIHSS) score at 24 h. Results: Of 986 patients, 843 (85.5%; median age 72 years, 56.7% male) had complete data and were included in the study analysis. Median baseline NIHSS score was 17 (IQR: 12-21). Median imaging follow-up time was 24 h (IQR 20-28). Median 24 h NIHSS score was 11 (5-17); 34% of patients had mRS 0-2 at 90 days. Median FIV was 30.2 mL (12.5-120.8 mL). FIV was significantly associated with 90-day mRS (concordance = 0.819, p < 0.001) and NIHSS at 24 h (concordance = 0.722, p < 0.001). cFIV, HT, AD, and IG were also significantly associated with good clinical outcomes in both 90-day mRS (concordance = 0.702, p < 0.001; 0.660, p < 0.001; 0.591, p = 0.002; and 0.663, p < 0.001, respectively) and NIHSS at 24 h (0.774, p < 0.001; 0.652, p = 0.004 L; 0.694, p < 0.001; and 0.716, p < 0.001, respectively). In multivariate analysis, FIV remained strongly associated with 90-day mRS. FIV showed a bimodal distribution consistent with success/failure of recanalization during thrombectomy. Conclusion: Of the algorithm outputs assessed, FIV was most strongly associated with clinical outcomes. Ischemic injury, HT, edema and IG were also independently significantly associated with clinical outcome. This study validates the prognostic significance of automated FIV and its composites as mechanistic endpoints to improve early-stage trials of therapeutics in AIS.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30210 - Clinical neurology
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2025
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Frontiers in Neurology
ISSN
1664-2295
e-ISSN
1664-2295
Volume of the periodical
16
Issue of the periodical within the volume
March
Country of publishing house
CH - SWITZERLAND
Number of pages
11
Pages from-to
1483138
UT code for WoS article
001457345600001
EID of the result in the Scopus database
2-s2.0-105001639127