Evidence map›Paper›PMID 42110963›Full record

ArticleOpen life sciences2026

Identification and validation of a pyroptosis-related gene signature in intracranial aneurysm.

Yang Liu, Yuanchi Cheng, Qian Li, Delong Wang

Abstract read
In one paragraph

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

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yang LiuDepartment of Neurology, Minhang Hospital, Fudan University, Shanghai, China.ORCID https://orcid.org/0000-0001-5939-572X
Yuanchi ChengDepartment of Neurosurgery, Shanghai Jiao Tong University Affiliated Sixth People's Hospital South Campus.
Qian LiDepartment of Neurology, Minhang Hospital, Fudan University, Shanghai, China.ORCID https://orcid.org/0009-0005-7616-2991
Delong WangDepartment of Neurology, Minhang Hospital, Fudan University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intracranial aneurysm (IA) is a life-threatening cerebrovascular disorder, the underlying molecular mechanisms of which remain incompletely elucidated. Pyroptosis, a pro-inflammatory form of programmed cell death, has been implicated in various vascular pathologies. However, its role in the pathogenesis of IA remains largely unclear. In this study, we identified and validated a pyroptosis-related gene signature linked to IA using GEO dataset. Differential expression analysis and pathway enrichment methods revealed key pyroptosis-related markers, including CASP8, NOD2, PYCARD, which were strongly associated with IA progression. Functional analysis highlighted their involvement in inflammatory and immune pathways, particularly in promoting vascular remodeling through pyroptosis-driven mechanisms. Machine learning approaches refined these markers into a robust predictive signature. Validation in independent cohorts confirmed their diagnostic and prognostic potential for IA. Moreover, we validated the upregulation of these genes and found the activation of CASP8 in clinical IA samples. Our findings provide novel insights into the molecular underpinnings of IA, offering a framework for the development of pyroptosis-based biomarkers and therapeutic strategies aimed at early detection and targeted intervention in IA management.

Indexed as

caspase 8immune infiltrationinflammationintracranial aneurysm (IA)pyroptosis

Identifiers

PMID42110963
PMCPMC13150365

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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.