Evidence map›Paper›PMID 36381288›Full record

ArticleResearch and practice in thrombosis and haemostasis2022

Lower levels of vWF are associated with lower risk of cardiovascular disease.

Pauline C S van Paridon, Marina Panova-Noeva, Rene van Oerle, Andreas Schulz, Jürgen H Prochaska, Natalie Arnold, Irene Schmidtmann, Manfred Beutel, Norbert Pfeiffer, Thomas Münzel and 4 more

Open access · goldAbstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Silencing of the von Willebrand factor gene in proatherothromboticResearch and practice in thrombosis and haemostasis · 2025
    Article
  5. Review
  6. Article
  7. Lower levels of vWF are associated with lower risk of cardiovascular disease.Research and practice in thrombosis and haemostasis · 2022
    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 at 2 institutions in 2 countries.

Pauline C S van ParidonLaboratory for Clinical Thrombosis and Hemostasis, Department of Internal Medicine, Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center Maastricht The Netherlands.
Marina Panova-NoevaCenter for Thrombosis and Hemostasis (CTH) University Medical Center of the Johannes Gutenberg-University Mainz Mainz Germany.ORCID https://orcid.org/0000-0003-2155-8030
Rene van OerleLaboratory for Clinical Thrombosis and Hemostasis, Department of Internal Medicine, Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center Maastricht The Netherlands.
Andreas SchulzPreventive Cardiology and Preventive Medicine, Center for Cardiology University Medical Center of the Johannes Gutenberg-University Mainz Mainz Germany.
Jürgen H ProchaskaCenter for Thrombosis and Hemostasis (CTH) University Medical Center of the Johannes Gutenberg-University Mainz Mainz Germany.
Natalie ArnoldPreventive Cardiology and Preventive Medicine, Center for Cardiology University Medical Center of the Johannes Gutenberg-University Mainz Mainz Germany.
Irene SchmidtmannInstitute of Medical Biostatistics, Epidemiology and Informatics University Medical Center of the Johannes Gutenberg-University Mainz Mainz Germany.
Manfred BeutelDepartment of Psychosomatic Medicine and Psychotherapy University Medical Center of the Johannes Gutenberg-University Mainz Mainz Germany.
Norbert PfeifferDepartment of Ophthalmology University Medical Center of the Johannes Gutenberg-University Mainz Mainz Germany.
Thomas MünzelDZHK (German Center for Cardiovascular Research) Partner Site RhineMain Mainz Germany.
Karl J LacknerDZHK (German Center for Cardiovascular Research) Partner Site RhineMain Mainz Germany.ORCID https://orcid.org/0000-0002-1985-7931
Hugo Ten CateLaboratory for Clinical Thrombosis and Hemostasis, Department of Internal Medicine, Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center Maastricht The Netherlands.ORCID https://orcid.org/0000-0001-7796-4463
Philipp S WildCenter for Thrombosis and Hemostasis (CTH) University Medical Center of the Johannes Gutenberg-University Mainz Mainz Germany.
Henri M H SpronkLaboratory for Clinical Thrombosis and Hemostasis, Department of Internal Medicine, Cardiovascular Research Institute Maastricht (CARIM) Maastricht University Medical Center Maastricht The Netherlands.ORCID https://orcid.org/0000-0002-3858-334X
Johannes Gutenberg University Mainz · DEMaastricht University Medical Centre · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: The current study was undertaken to prospectively explore whether having low levels of von Willebrand factor (vWF) antigen and vWF activity reduce the risk for cardiovascular disease and death. Methods: VWF antigen and vWF activity were measured by enzyme-linked immunosorbent assay and an immunological-based assay, respectively, in a subsample of 4857 individuals aged between 35 and 74 years old, enrolled between April 2007 and October 2008 in the population-based Gutenberg Health Study. VWF antigen and activity below the 20th percentile was set as a measure of "low vWF." Adjusted robust Poisson regression models were used to analyze the relation between low vWF and the incidence of cardiovascular disease (CVD). Consequent adjusted cox regression models as well as cumulative incidence plots were calculated to explore the relation between all-cause and cardiovascular mortality and low vWF. Results: VWF activity levels <20th percentile (i.e., <76.2%) were associated with a decreased relative risk for CVD (RR: 0.59, 95% CI: 0.37-0.95), despite adjusting for age and sex. After adjusting for levels of F-VIII, the association persisted (RR: 0.60, 95% CI: 0.36-0.99). The cumulative incidence plots demonstrated that vWF antigen <20th percentile significantly correlated with decreased cardiovascular mortality. VWF antigen<20th percentile (i.e., <83%) was significantly associated with lower risk of all-cause mortality, despite adjusting for clinical factors (RR: 61, 95% CI: 0.41-0.91). Conclusion: The study demonstrated that having low vWF activity levels were associated with a lower risk for CVD. Additionally, it revealed a decreased risk of cardiovascular and all-cause mortality in individuals with low levels of vWF antigen, shining new light on vWF as a potential target for novel therapies.

Indexed as

cardiovascular diseasesgeneral populationincidencethrombosisvon Willebrand factor

Identifiers

PMID36381288
PMCPMC9637545
OpenAlexW4308750675

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.