Evidence map›Paper›PMID 41586867›Full record

ArticleEuropean radiology experimental2026

An endovascular porcine model of abdominal aortic aneurysm for interventional radiology research.

Marie-Luise Helene Hildegard Ranner-Hafferl, Dilyana Branimirova Mangarova, Jennifer Mein, Jennifer Lilly Heyl, Jana Möckel, Dirk Schnapauff, Timo Alexander Auer, Federico Collettini, Jan Ole Kaufmann, Lisa Christine Adams and 4 more

Abstract read
In one paragraph

Article in European radiology experimental, 2026. 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

14 authors.

Marie-Luise Helene Hildegard Ranner-HafferlDepartment of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany. marie.ranner-hafferl@charite.de.ORCID http://orcid.org/0009-0001-5355-9030
Dilyana Branimirova MangarovaDepartment of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Jennifer MeinDepartment of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Jennifer Lilly HeylDepartment of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Jana MöckelDepartment of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Dirk SchnapauffDepartment of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Timo Alexander AuerDepartment of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Federico CollettiniDepartment of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Jan Ole KaufmannDepartment of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Lisa Christine AdamsDepartment of Diagnostic and Interventional Radiology, Technical University of Munich, Munich, Germany.
Marcus Richard MakowskiDepartment of Diagnostic and Interventional Radiology, Technical University of Munich, Munich, Germany.
Bernd HammDepartment of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Avan Kader *Department of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Julia Brangsch *Department of Radiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.

Funding

Deutsche Forschungsgemeinschaft 372486779
6 · The paper itself

Abstract

objectiveAbdominal aortic aneurysm (AAA) remains a life-threatening condition with few large-animal disease models. We aimed to develop a fully endovascular porcine AAA model for radiology research, reducing surgical trauma and improving reproducibility versus laparotomy-based models. MATERIALS AND

methodsFourteen female German Landrace swine (n = 14, 30-40 kg) underwent angiography-guided intervention. The animals' infrarenal aorta was dilated by ~30% via balloon catheter, then collagenase (6,000 IU), elastase (500 IU), and 25% calcium chloride (0.5 mL) were locally incubated to weaken the vessel wall. Eight animals were included in the study; group 1 (n = 4) was euthanized at 2 weeks, and group 2 (n = 4) at 4 weeks. Aortic diameter was measured weekly by ultrasound; ex vivo histology, immunofluorescence, and western blot assessed remodeling and inflammation.

resultsProgressive aneurysm expansion was observed, with diameters of 1.32 ± 0.08 cm (mean ± standard deviation) at 1 week post-intervention, 1.59 ± 0.06 cm at 2 weeks, 1.81 ± 0.10 cm at 3 weeks, and 1.94 ± 0.19 cm at 4 weeks (baseline: 0.74 ± 0.08 cm; p < 0.001). Experimental groups' macrophages increased (group 1, 15.12 ± 3.88%; group 2, 16.65 ± 5.27%) compared to control (0.66 ± 0.27%, p = 0.012 and p = 0.021, respectively). Vascular smooth muscle cells were reduced across interventional groups (45.97 ± 17.26% versus control 80.94 ± 14.26%, p = 0.005).

conclusionsThis porcine AAA model replicates human disease features with a fully endovascular workflow, offering a valuable platform for evaluation of novel imaging techniques and interventional therapies. RELEVANCE STATEMENT: This study presents a fully endovascular porcine model of abdominal aortic aneurysm for translational research in interventional radiology and imaging. By enabling aneurysm induction entirely through catheter-based techniques, the model could provide a clinically relevant platform for future evaluation of novel endovascular devices and intraluminal therapeutics. KEY POINTS: This study established a fully endovascular, translational porcine model of abdominal aortic aneurysm. The model exhibited a significant mean aneurysmal dilation of about 161% at 4 weeks and 107% at 2 weeks. Serial ultrasound confirmed consistent aneurysm expansion and reproducible growth patterns in surviving animals. Ex vivo analyses demonstrated inflammation and extracellular-matrix damage, mirroring key features of human abdominal aortic aneurysm pathology. This fully catheter-based workflow provides a practical preclinical platform for evaluating imaging techniques and endovascular therapies.

Indexed as

Aortic Aneurysm, AbdominalDisease Models, AnimalEndovascular ProceduresRadiology, InterventionalAnimalsAorta, AbdominalFemaleSwineUltrasonographyAortic aneurysm (abdominal)Disease models (animal)Endovascular proceduresExtracellular matrixSwine

Identifiers

PMID41586867
PMCPMC12834893

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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.