Evidence map›Paper›PMID 31245608›Full record

ArticleBMJ open ophthalmology2019

Evaluation of the safety and effectiveness of oral propranolol in patients with von Hippel-Lindau disease and retinal hemangioblastomas: phase III clinical trial.

Beatriz González-Rodríguez, Karina Villar Gómez de Las Heras, Daniel T Aguirre, Luis Rodríguez-Padial, Virginia Albiñana, Lucía Recio-Poveda, Angel M Cuesta, Luisa Mª Botella, Rosa María Jiménez-Escribano

Open access · goldAbstract read
In one paragraph

Article in BMJ open ophthalmology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 35% of its field
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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Proteostasis Modulation in Germline Missense von Hippel Lindau Disease.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  5. Review
  6. Review
  7. Review
  8. The Role of Propranolol as a Repurposed Drug in Rare Vascular Diseases.International journal of molecular sciences · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. 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

9 authors at 5 institutions in 1 country.

Beatriz González-RodríguezOphthalmology, Retina Service, Complejo Hospitalario de Toledo, Servicio de Salud de Castilla-La Mancha, Toledo, Spain.
Karina Villar Gómez de Las HerasDG Asistencia Sanitaria, Servicio de Salud de Castilla-La Mancha, Toledo, Spain.ORCID 0000-0002-8346-6193
Daniel T AguirreNeurosurgery, Familial Neuro-Oncology Unit, Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
Luis Rodríguez-PadialCardiology, Complejo Hospitalario de Toledo, Servicio de Salud de Castilla-La Mancha, Toledo, Spain.
Virginia AlbiñanaCentro de Investigaciones Biológicas-CIB, Centro Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
Lucía Recio-PovedaCentro de Investigaciones Biológicas-CIB, Centro Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
Angel M CuestaCentro de Investigaciones Biológicas-CIB, Centro Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
Luisa Mª BotellaCentro de Investigaciones Biológicas-CIB, Centro Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
Rosa María Jiménez-EscribanoOphthalmology, Retina Service, Complejo Hospitalario de Toledo, Servicio de Salud de Castilla-La Mancha, Toledo, Spain.
Centre for Biomedical Network Research on Rare Diseases · ESServicio de Salud de Castilla La Mancha · ESAlianza Española de Familias de Von Hippel Lindau · ESCentro de Investigaciones Biológicas Margarita Salas · ESHospital Universitario Fundación Jiménez Díaz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundvon Hippel-Lindau disease (VHL) is a multisystem cancer syndrome caused by mutations in the

methodsSeven patients were included. All patients took a daily dose of 120 mg of propranolol for 1 year. Clinical variables were assessed at baseline, and at 1, 3, 6, 9 and 12 months. The primary endpoint of the study was the number and size of retinal hemangioblastomas. On every visit, retinal outcomes and blood biomarkers (such as vascular endothelial growth factor (VEGF) and miR210) were analysed.

resultsNumber and size of retinal hemangioblastomas remained stable in all patients. All of them had initially increased levels of VEGF and miR210. There was a gradual reabsorption of retinal exudation in two patients, correlating with a progressive decrease of both biomarkers. The only adverse effect reported was hypotension in one patient.

conclusionsPropranolol could be used to treat retinal hemangioblastomas in VHL patients, although more studies are needed to determine the ideal dose and long-term effect. VEGF and miR210 should be explored as biomarkers of disease activity. As far as we know, these are the first biomarkers proposed to monitor the VHL disease activity. TRIAL REGISTRATION NUMBER: 2014-003671-30.

Indexed as

hemangioblastomahypoxia-inducible factorspropranololretinavon Hippel-Lindau

Identifiers

PMID31245608
PMCPMC6557078
OpenAlexW2947571379

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

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.