Evidence map›Paper›PMID 30713844›Full record

ReviewFrontiers in cardiovascular medicine2018

Endogenous Calcification Inhibitors in the Prevention of Vascular Calcification: A Consensus Statement From the COST Action EuroSoftCalcNet.

Magnus Bäck, Tamas Aranyi, M Leonor Cancela, Miguel Carracedo, Natércia Conceição, Georges Leftheriotis, Vicky Macrae, Ludovic Martin, Yvonne Nitschke, Andreas Pasch and 8 more

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03858413 (Correlation of a-Klotho Levels With the Severity of Calcification in the Coronary Arteries and Aortic Valve in Patients With Chronic Kidney Disease), which is not on this map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
13.1field-weighted citation impact, top 1% 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.

NCT03858413 completednot on this map

Correlation of a-Klotho Levels With the Severity of Calcification in the Coronary Arteries and Aortic Valve in Patients With Chronic Kidney Disease

TypeobservationalSponsorRoyal Brompton & Harefield NHS Foundation TrustRan2016 to 2018Enrolled60ConditionsVascular Calcification, Chronic Kidney DiseasesArmsNo intervention
3 · Its place in the literature

Who cites it

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 100 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Predictor Role ofMedicina (Kaunas, Lithuania) · 2025
    Article
  6. Soft tissue calcifications in chronic kidney disease-beyond the vasculature.Pflugers Archiv : European journal of physiology · 2025
    Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Observational
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

18 authors at 14 institutions in 10 countries.

Magnus BäckTranslational Cardiology, Center for Molecular Medicine, Karolinska University Hospital Stockholmt, Stockholm, Sweden.
Tamas AranyiResearch Center for Natural Sciences, Institute of Enzymology, Hungarian Academy of Sciences, Budapest, Hungary.
M Leonor CancelaDepartment of Biomedical Sciences and Medicine, Algarve Biomedical Centre, Centre of Marine Sciences/CCMAR, University of Algarve, Faro, Portugal.
Miguel CarracedoTranslational Cardiology, Center for Molecular Medicine, Karolinska University Hospital Stockholmt, Stockholm, Sweden.
Natércia ConceiçãoDepartment of Biomedical Sciences and Medicine, Algarve Biomedical Centre, Centre of Marine Sciences/CCMAR, University of Algarve, Faro, Portugal.
Georges LeftheriotisLP2M, University of Nice-Sophia Antipolis and Vascular Physiology and Medicine, University Hospital of Nice, Nice, France.
Vicky MacraeThe Roslin Institute and Royal School of Veterinary Studies, University of Edinburgh, Edinburgh, United Kingdom.
Ludovic MartinPXE Reference Center, Angers University Hospital, Angers, France.
Yvonne NitschkeDepartment of General Pediatrics, Münster University Children's Hospital, Münster, Germany.
Andreas PaschCalciscon AG, Nidau, Switzerland.
Daniela QuaglinoDepartment of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Frank RutschDepartment of General Pediatrics, Münster University Children's Hospital, Münster, Germany.
Catherine ShanahanBritish Heart Foundation Centre of Research Excellence, James Black Centre, School of Cardiovascular Medicine and Sciences, King's College London, London, United Kingdom.
Victor SorribasLaboratory of Molecular Toxicology, Veterinary Faculty, University of Zaragoza, Zaragoza, Spain.
Flora SzeriResearch Center for Natural Sciences, Institute of Enzymology, Hungarian Academy of Sciences, Budapest, Hungary.
Pedro ValdivielsoInternal Medicine, Instituto de Investigación Biomédica (IBIMA), Virgen de la Victoria University Hospital, Universidad de Málaga, Málaga, Spain.
Olivier VanakkerCenter for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Hervé KempfUMR 7365 CNRS-Université de Lorraine, IMoPA, Vandoeuvre-lès-Nancy, France.
Karolinska University Hospital · SEUniversity Hospital Münster · DEUniversity of Algarve · PTCentre National de la Recherche Scientifique · FRGhent University Hospital · BEInstitute of Molecular Life Sciences · HUInstituto de Investigación Biomédica de Málaga · ESKing's College London · GBRoslin Institute · GBThomas Jefferson University · USUniversidad de Zaragoza · ESUniversité Côte d'Azur · FRUniversité d'Angers · FRUniversity of Modena and Reggio Emilia · IT

Funding

British Heart Foundation RG/17/2/32808
6 · The paper itself

Abstract

The physicochemical deposition of calcium-phosphate in the arterial wall is prevented by calcification inhibitors. Studies in cohorts of patients with rare genetic diseases have shed light on the consequences of loss-of-function mutations for different calcification inhibitors, and genetic targeting of these pathways in mice have generated a clearer picture on the mechanisms involved. For example, generalized arterial calcification of infancy (GACI) is caused by mutations in the enzyme ecto-nucleotide pyrophosphatase/phosphodiesterase-1 (eNPP1), preventing the hydrolysis of ATP into pyrophosphate (PP

Indexed as

arterial calcificationfetuingla proteinsklothoosteopontinosteoprotegerinpyrophosphate

Identifiers

PMID30713844
PMCPMC6345677
OpenAlexW2910000388

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.