Evidence map›Paper›PMID 40502739›Full record

ArticleResearch square2025

Evaluation of Radiogenomics for Risk Stratification of Intracranial Aneurysms: A Pilot Study.

Sricharan S Veeturi, Kerry E Poppenberg, Nandor K Pinter, Vinay Jaikumar, Elad I Levy, Adnan H Siddiqui, Vincent M Tutino

Abstract readPreprint
In one paragraph

Article in Research square, 2025. 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

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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

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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

5 · Who and what money

Authors and funding

7 authors.

Sricharan S VeeturiUniversity at Buffalo, State University of New York.
Kerry E PoppenbergUniversity at Buffalo, State University of New York.
Nandor K PinterUniversity at Buffalo, State University of New York.
Vinay JaikumarUniversity at Buffalo, State University of New York.
Elad I LevyUniversity at Buffalo, State University of New York.
Adnan H SiddiquiUniversity at Buffalo, State University of New York.
Vincent M TutinoUniversity at Buffalo, State University of New York.

Funding

Development of a Molecular Diagnostic to Identify Dangerous Intracranial AneurysmsR44NS115314 · NINDS · NEUROVASCULAR DIAGNOSTICS, INC. · PI POPPENBERG, KERRY, TUTINO, VINCENT MATTHEW · 2023 to 2025
$2.9M
Virtual Intervention of Intracranial AneurysmsR01NS091075 · NINDS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MENG, HUI · 2015 to 2019
$1.7M
Optimizing Approaches to Endovascular Therapy of Acute Ischemic StrokeR21NS109575 · NINDS · UNIVERSITY OF SOUTH FLORIDA · PI MOKIN, MAXIM · 2019 to 2019
$420k
Molecular Biomarkers of Dangerous Intracranial AneurysmsR43NS115314 · NINDS · NEUROVASCULAR DIAGNOSTICS, INC. · PI TUTINO, VINCENT MATTHEW · 2019 to 2019
$225k
NINDS NIH HHS R01 NS091075NINDS NIH HHS R21 NS109575NINDS NIH HHS R43 NS115314NINDS NIH HHS R44 NS115314
6 · The paper itself

Abstract

Aneurysm wall enhancement (AWE) has emerged as an imaging biomarker, which could help in risk stratification of intracranial aneurysms (IAs) and also shed light on local pathobiology of the IA wall. In this pilot study, we explored the potential of a radiogenomics approach by combining blood-based biomarkers and AWE for better risk stratification of IAs. Patient specific vessel wall imaging scans and whole blood samples were obtained, and IAs were classified as high-risk or low-risk using two different metrics: symptomatic status (3 symptomatic vs. 13 asymptomatic) and PHASES score (4 with a high score vs. 12 with a low score). Radiomics features (RFs) were extracted from the pre- and post-contrast MRI for all IA sac walls, and significantly different RFs were identified through univariate analysis. RNA sequencing from whole blood samples for these patients was also performed to identify differentially expressed genes (DEGs) between high and low-risk IA groups. Using both risk metrics, we performed principal component analysis (PCA), clustering analysis, and correlation analysis between RFs and genes. Lastly, ontological analyses were carried out to investigate biological mechanisms associated with the DEGs. Our analysis of 16 IAs identified 22 RFs that were significantly different between symptomatic and asymptomatic IAs and 97 genes with at least a 2-fold change and a p-value < 0.01. Examining risk with respect to PHASES score, we identified 10 significant radiomics features and 38 differentially expressed genes. Furthermore, we found a significant correlation between 15 unique RFs and 49 DEGs. Through principal component analysis, we found that DEGs only and radiogenomics features produced a better separation between high- and low-risk, for both risk metrics, than RFs alone. We demonstrated that a radiogenomics approach can help in better risk stratification of IAs.

Identifiers

PMID40502739
PMCPMC12154131

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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.