Evidence map›Paper›PMID 29767844›Full record

ArticleBritish journal of haematology2018

Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand disease.

Ferdows Atiq, Karina Meijer, Jeroen Eikenboom, Karin Fijnvandraat, Eveline P Mauser-Bunschoten, Karin P M van Galen, Marten R Nijziel, Paula F Ypma, Joke de Meris, Britta A P Laros-van Gorkom and 5 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in British journal of haematology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03521583 (Von Willebrand Disease in the Netherlands - Prospective Study), which is not on this map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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.

NCT03521583 unknown statusnot on this mapstarted 2019, after this paper: background citation

Von Willebrand Disease in the Netherlands - Prospective Study (WiN-Pro)

TypeobservationalSponsorErasmus Medical CenterRan2019 to 2022Enrolled1,100ConditionsVon Willebrand Disease
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Diagnostic pitfalls and conundrums in type 1 von Willebrand disease.Hematology. American Society of Hematology. Education Program · 2022
    Article
  10. How to manage bleeding disorders in aging patients needing surgery.Hematology. American Society of Hematology. Education Program · 2021
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
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  20. 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

15 authors at 8 institutions in 1 country.

Ferdows AtiqDepartment of Haematology, Erasmus University Medical Centre, Rotterdam, the Netherlands.ORCID 0000-0002-3769-9148
Karina MeijerDepartment of Haematology, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Jeroen EikenboomDepartment of Thrombosis and Haemostasis, Leiden University Medical Centre, Leiden, the Netherlands.
Karin FijnvandraatPediatric Haematology, Emma Children's Hospital-Academic Medical Centre, Amsterdam, the Netherlands.
Eveline P Mauser-BunschotenVan Creveldkliniek, University Medical Centre University Utrecht, Utrecht, the Netherlands.
Karin P M van GalenVan Creveldkliniek, University Medical Centre University Utrecht, Utrecht, the Netherlands.ORCID 0000-0003-3251-8595
Marten R NijzielDepartment of Haematology, Radboud University Medical Centre, Nijmegen, the Netherlands.
Paula F YpmaDepartment of Haematology, Haga Hospital, The Hague, the Netherlands.
Joke de MerisNetherlands Haemophilia Society, Leiden, the Netherlands.
Britta A P Laros-van GorkomDepartment of Haematology, Radboud University Medical Centre, Nijmegen, the Netherlands.
Johanna G van der BomDepartment of Clinical Epidemiology, Leiden University Medical Centre, Leiden, the Netherlands.
Moniek P de MaatDepartment of Haematology, Erasmus University Medical Centre, Rotterdam, the Netherlands.
Marjon H CnossenDepartment of Pediatric Haematology, Erasmus University Medical Centre-Sophia Children's Hospital, Rotterdam, the Netherlands.
Frank W G LeebeekDepartment of Haematology, Erasmus University Medical Centre, Rotterdam, the Netherlands.
WiN study group
Leiden University Medical Center · NLRadboud University Nijmegen · NLUniversity Medical Center Utrecht · NLEmma Kinderziekenhuis · NLErasmus MC - Sophia Children’s Hospital · NLHaga Hospital · NLNetherlands Haemophilia SocietyUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some comorbidities, such as hypertension, are associated with higher von Willebrand factor (VWF) levels in the general population. No studies have been conducted to assess this association in patients with von Willebrand disease (VWD). Therefore, we studied this association in patients with type 1 (n = 333) and type 2 (n = 203) VWD from the 'WiN" study. VWF antigen (VWF:Ag) was higher in type 1 VWD patients with hypertension [difference: 0·23 iu/ml, 95% confidence interval (CI): 0·11-0·35], diabetes mellitus (0·11 iu/ml, 95% CI: -0·02 to 0·23), cancer (0·14 iu/ml, 95% CI: 0·03-0·25) and thyroid dysfunction (0·14 iu/ml, 95% CI: 0·03-0·26) than in patients without these comorbidities (all corrected for age, sex and blood group). Similar results were observed for VWF collagen binding capacity (VWF:CB), VWF activity as measured by the VWF monoclonal antibody assay (VWF:Ab) and factor VIII (FVIII) coagulant activity (FVIII:C). In type 1 VWD, age was associated with higher VWF:Ag (0·03 iu/ml; 95% CI: 0·01-0·04), VWF:CB (0·02 iu/ml; 95% CI: 0·00-0·04), VWF:Ab (0·04 iu/ml; 95% CI: 0·02-0·06) and FVIII:C (0·03 iu/ml; 95% CI: 0·01-0·06) per decade increase. After adjustment for relevant comorbidities, these associations were no longer significant. Despite the higher VWF and FVIII levels, type 1 VWD patients with comorbidities had more bleeding episodes, particularly during surgery. There was no association between comorbidities and VWF/FVIII levels or bleeding phenotype in type 2 VWD patients. In conclusion, comorbidities are associated with higher VWF and FVIII levels in type 1 VWD and may explain the age-related increase of VWF and FVIII levels.

Indexed as

AdolescentAdultAgedAged, 80 and overAgingComorbidityCross-Sectional StudiesDiabetes MellitusFactor VIIIFemaleHumansHypertensionMaleMiddle AgedNeoplasmsNetherlandsFactor VIIIvon Willebrand FactorcancerdiabeteselderlyVWDVWF

Identifiers

PMID29767844
PMCPMC6032952
OpenAlexW2804578743

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

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.