Evidence map›Paper›PMID 41463009›Full record

ArticleBiomedicines2025

Disrupted Vessels-Connected Voices: Why Patient Partnership and Cross-Disease Collaboration Are Essential for Accelerating HHT Research.

Irina Kruetzner, Freya Droege, Simone Kesten, Urban Geisthoff, Christian Hiepen

Abstract readComment
In one paragraph

Article in Biomedicines, 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Irina KruetznerWorking Group Biomedicine and Cellular Biomechanics, Unit of Molecular Biology, Department of Engineering and Natural Sciences, Campus Recklinghausen, Westphalian University of Applied Sciences Gelsenkirchen, Bocholt, Recklinghausen, August-Schmidt-Ring 10, 45665 Recklinghausen, Germany.
Freya DroegeDepartment of Otorhinolaryngology, Head and Neck Surgery and VASCERN HHT Reference Centre, Essen University Hospital, University Duisburg-Essen, Hufelandstr. 55, 45147 Essen, Germany.ORCID 0000-0001-8811-507X
Simone KestenMorbus Osler Selbsthilfe e.V., Scherenbergstr. 6, 10439 Berlin, Germany.
Urban GeisthoffMorbus Osler Selbsthilfe e.V., Scherenbergstr. 6, 10439 Berlin, Germany.
Christian HiepenWorking Group Biomedicine and Cellular Biomechanics, Unit of Molecular Biology, Department of Engineering and Natural Sciences, Campus Recklinghausen, Westphalian University of Applied Sciences Gelsenkirchen, Bocholt, Recklinghausen, August-Schmidt-Ring 10, 45665 Recklinghausen, Germany.ORCID 0000-0001-7345-6496

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rare vascular diseases such as hereditary haemorrhagic telangiectasia (HHT) represent a big challenge in biomedicine: complex pathomechanisms, limited patient material, and fragmented research communities slow down therapeutic progress. We argue that two elements are pivotal to bypass this problem. First, genuine partnership with patients-ranging from biospecimen donation to agenda setting-can unlock critical resources and align research with real-world needs. Second, molecular intersections between HHT and related pathologies call for coordinated, cross-disease programmes rather than isolated efforts. Recent multi-stakeholder gatherings hosted by patient organisations in Germany and elsewhere, such as the Second Scientific Symposium by the German HHT self-help group (Morbus Osler Selbsthilfe e.V.) in May 2025, have shown that when clinicians, basic scientists from different disciplines, and affected families co-design research questions, novel in vitro models can be generated more accurately, and pragmatic clinical trials emerge. Here, we outline actual opportunities for patient-integrated cellular model systems, shared biobanking, and comparative approaches across vascular malformation syndromes. In our opinion, letting informed and well-organised patient communities assemble such meetings opens unique opportunities twofold: on the one hand, the field can finally break out of its disease-specific silos; on the other hand, the development of novel HHT therapies could be accelerated by learning from progress in related pathologies.

Indexed as

ALK1BMPCCMendoglinendothelial cellsHHTMorbus OslerTGF-βvascular malformations

Identifiers

PMID41463009
PMCPMC12730726

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Registered trials

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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.