Evidence map›Paper›PMID 26516910›Full record

Trial reportNutrients2015

Menaquinone-7 Supplementation to Reduce Vascular Calcification in Patients with Coronary Artery Disease: Rationale and Study Protocol (VitaK-CAC Trial).

Liv M Vossen, Leon J Schurgers, Bernard J van Varik, Bas L J H Kietselaer, Cees Vermeer, Johannes G Meeder, Braim M Rahel, Yvonne J M van Cauteren, Ge A Hoffland, Roger J M W Rennenberg and 3 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Nutrients, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.9field-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.

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

35 citing papers in PubMed, 63 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. High-level production of vitamin K2 inSynthetic and systems biotechnology · 2026
    Article
  5. Review
  6. Review
  7. Article
  8. Vitamin KOpen heart · 2021
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Early vascular ageing in chronic kidney disease: impact of inflammation, vitamin K, senescence and genomic damage.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2020
    Review
  17. Review
  18. Review
  19. Observational
  20. Review
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

13 authors at 3 institutions in 1 country.

Liv M VossenDepartment of Internal Medicine, Maastricht University Medical Centre (MUMC+), Maastricht 6229HX, The Netherlands. liv.vossen@mumc.nl.
Leon J SchurgersDepartment of Biochemistry, Cardiovascular Research Institute Maastricht (CARIM), University of Maastricht, Maastricht 6229ER, The Netherlands. l.schurgers@maastrichtuniversity.nl.
Bernard J van VarikDepartment of Internal Medicine, Maastricht University Medical Centre (MUMC+), Maastricht 6229HX, The Netherlands. b.vanvarik@maastrichtuniversity.nl.
Bas L J H KietselaerDepartments of Cardiology and Radiology, Maastricht University Medical Centre (MUMC+), Maastricht 6229HX, The Netherlands. b.kietselaer@mumc.nl.
Cees VermeerGroup VitaK, Maastricht University, Maastricht 6229EV, The Netherlands. c.vermeer@vitak.com.
Johannes G MeederDepartment of Cardiology, VieCuri Medical Centre, Venlo 5912 BL, The Netherlands. jmeeder@viecuri.nl.
Braim M RahelDepartment of Cardiology, VieCuri Medical Centre, Venlo 5912 BL, The Netherlands. brahel@viecuri.nl.
Yvonne J M van CauterenDepartment of Cardiology, VieCuri Medical Centre, Venlo 5912 BL, The Netherlands. yvonne.cauteren@mumc.nl.
Ge A HofflandDepartment of Radiology, VieCuri Medical Centre, Venlo 5912BL, The Netherlands. ghoffland@viecuri.nl.
Roger J M W RennenbergDepartment of Internal Medicine, Maastricht University Medical Centre (MUMC+), Maastricht 6229HX, The Netherlands. r.rennenberg@mumc.nl.
Koen D ReesinkDepartment of Biochemistry, Cardiovascular Research Institute Maastricht (CARIM), University of Maastricht, Maastricht 6229ER, The Netherlands. k.reesink@maastrichtuniversity.nl.
Peter W de LeeuwDepartment of Internal Medicine, Maastricht University Medical Centre (MUMC+), Maastricht 6229HX, The Netherlands. p.deleeuw@maastrichtuniversity.nl.
Abraham A KroonDepartment of Internal Medicine, Maastricht University Medical Centre (MUMC+), Maastricht 6229HX, The Netherlands. aa.kroon@mumc.nl.
Maastricht University Medical Centre · NLVieCuri Medisch Centrum · NLMaastricht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronary artery calcification (CAC) develops early in the pathogenesis of atherosclerosis and is a strong and independent predictor of cardiovascular disease (CVD). Arterial calcification is caused by an imbalance in calcification regulatory mechanisms. An important inhibitor of calcification is vitamin K-dependent matrix Gla protein (MGP). Both preclinical and clinical studies have shown that inhibition of the vitamin K-cycle by vitamin K antagonists (VKA) results in elevated uncarboxylated MGP (ucMGP) and subsequently in extensive arterial calcification. This led us to hypothesize that vitamin K supplementation may slow down the progression of calcification. To test this, we designed the VitaK-CAC trial which analyses effects of menaquinone-7 (MK-7) supplementation on progression of CAC. The trial is a double-blind, randomized, placebo-controlled trial including patients with coronary artery disease (CAD). Patients with a baseline Agatston CAC-score between 50 and 400 will be randomized to an intervention-group (360 microgram MK-7) or a placebo group. Treatment duration will be 24 months. The primary endpoint is the difference in CAC-score progression between both groups. Secondary endpoints include changes in arterial structure and function, and associations with biomarkers. We hypothesize that treatment with MK-7 will slow down or arrest the progression of CAC and that this trial may lead to a treatment option for vascular calcification and subsequent CVD.

Indexed as

Dietary SupplementsAdultArteriesCalciumCalcium-Binding ProteinsClinical ProtocolsCoronary Artery DiseaseDisease ProgressionDouble-Blind MethodExtracellular Matrix ProteinsHumansMatrix Gla ProteinResearch DesignVascular CalcificationVitamin K 2VitaminsCalciumCalcium-Binding ProteinsExtracellular Matrix ProteinsMatrix Gla Proteinmenaquinone 7Vitamin K 2Vitaminscoronary artery calcificationmatrix gla proteinmenaquinone-7vascular calcificationvitamin K2

Identifiers

PMID26516910
PMCPMC4663571
OpenAlexW1879989348

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LicenceCC BY
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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.