Evidence map›Paper›PMID 41787011›Full record

ArticleScientific reports2026

Unsupervised cluster analysis identifies risk profiles driving heterogeneity and survival patterns in aortic aneurysm patients.

Maria Elisabeth Leinweber, Fadi Taher, Miriam Kliewer, Afshin Assadian, Amun Hofmann

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Article in Scientific reports, 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

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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

5 authors.

Maria Elisabeth LeinweberDepartment of Vascular and Endovascular Surgery, Klinik Ottakring, Montleartstraße 37, 1160, Vienna, Austria.
Fadi TaherDepartment of Vascular and Endovascular Surgery, Klinik Ottakring, Montleartstraße 37, 1160, Vienna, Austria.
Miriam KliewerDepartment of Vascular and Endovascular Surgery, Klinik Ottakring, Montleartstraße 37, 1160, Vienna, Austria.
Afshin AssadianDepartment of Vascular and Endovascular Surgery, Klinik Ottakring, Montleartstraße 37, 1160, Vienna, Austria.
Amun HofmannDepartment of Vascular and Endovascular Surgery, Klinik Ottakring, Montleartstraße 37, 1160, Vienna, Austria. amungeorg.hofmann@gesundheitsverbund.at.

Funding

Austrian Society of Vascular Surgery 01-2024
6 · The paper itself

Abstract

Aortic aneurysms (AAs) are influenced by diverse modifiable and non-modifiable risk factors. The underlying heterogeneity in this patient population complicates efforts to optimize risk stratification. Phenomapping leverages unsupervised clustering algorithms to group similar patients based on phenotypic profiles and can identify homogenous clusters in complex data patterns. While clinical classification typically relies on aneurysm morphology and presentation, unsupervised phenomapping could uncover alternative, data-driven risk profiles. Unsupervised clustering (k-means) utilizing data from the UK Biobank was conducted. All patients recorded with aortic pathologies (ICD-10 group I71) were included. Clustering variables encompassed demographic and clinical parameters, emphasizing relevant comorbidities. The main analyses were conducted in abdominal AA, whereas validation analyses were conducted in the remaining aortic pathologies. The primary outcome was all-cause mortality. The study population consisted of 4623 participants (21.2% female), including abdominal (66.9%), thoracic (25.4%), and thoracoabdominal AA (0.5%), as well as aortic dissections (7.2%). Cardiovascular comorbidity emerged as the primary driver of cluster differentiation both in the main and validation analysis outweighing morphological differences. Survival analysis highlighted higher all-cause mortality rates in these multimorbid clusters. Cardiovascular and renal comorbidities can be leveraged in an informative comorbidity index. The non-linear increase in mortality risk may be indicative of the superimposed effects of the aortic pathology itself. Cardiorenal multimorbidity appears to be the most relevant separator between AA patients. However, the burden of disease associated with an aortic pathology itself relevantly impacts mortality risk estimation based on these comorbidities.

Indexed as

Aortic AneurysmAgedAortic Aneurysm, AbdominalCluster AnalysisClustering AlgorithmsComorbidityFemaleHumansMaleMiddle AgedRisk AssessmentRisk FactorsSurvival AnalysisUnited KingdomAneurysmAortic aneurysmCluster analysisOutcomesPhenomapping

Identifiers

PMID41787011
PMCPMC13076763

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