Evidence map›Paper›PMID 30759309›Full record

ArticleJournal of nephrology2019

Osteocalcin (bone GLA protein) levels, vascular calcifications, vertebral fractures and mortality in hemodialysis patients with diabetes mellitus.

Maria Fusaro, Maurizio Gallieni, Andrea Aghi, Maria Antonietta Rizzo, Giorgio Iervasi, Thomas L Nickolas, Fabrizio Fabris, Maria Cristina Mereu, Sandro Giannini, Stefania Sella and 12 more

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In one paragraph

Article in Journal of nephrology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Observational
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Vertebral fracture is associated with myocardial infarction in incident hemodialysis patients: a Korean nationwide population-based study.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2020
    Article
  10. Association Study betweenJournal of diabetes research · 2019
    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

22 authors at 12 institutions in 2 countries.

Maria FusaroNational Research Council (CNR), Institute of Clinical Physiology (IFC), Via G. Moruzzi 1, 56124, Pisa, PI, Italy. dante.lucia@libero.it.
Maurizio GallieniNephrology and Dialysis Unit, Department of Clinical and Biomedical Sciences 'Luigi Sacco', University of Milan, Milan, Italy.
Andrea AghiDepartment of Medicine, Clinica Medica 1, University of Padova, Padua, Italy.
Maria Antonietta RizzoNephrology and Dialysis Unit, Ospedale di Circolo di Busto Arsizio, ASST Valle Olona, Busto Arsizio, Italy.
Giorgio IervasiNational Research Council (CNR), Institute of Clinical Physiology (IFC), Via G. Moruzzi 1, 56124, Pisa, PI, Italy.
Thomas L NickolasDivision of Nephrology, Department of Medicine, Columbia University Medical Center, New York, NY, USA.
Fabrizio FabrisDepartment of Medicine, Clinica Medica 1, University of Padova, Padua, Italy.
Maria Cristina MereuNephrologist Independent Researcher, Cagliari, Italy.
Sandro GianniniDepartment of Medicine, Clinica Medica 1, University of Padova, Padua, Italy.
Stefania SellaDepartment of Medicine, Clinica Medica 1, University of Padova, Padua, Italy.
Andrea GiustiBone Clinic, Dipartimento delle Cure Geriatriche, Ortogeriatria e Riabilitazione, Ospedale Galliera, Genoa, Italy.
Annalisa PitinoNational Research Council (CNR), Institute of Clinical Physiology (IFC), Via G. Moruzzi 1, 56124, Pisa, PI, Italy.
Graziella D'ArrigoClinical Epidemiology and Physiopathology of Renal Diseases and Hypertension, CNR, Institute of Clinical Physiology, Reggio Calabria, Calabria, Italy.
Maurizio RossiniRheumatology Unit, Department of Medicine, , University of Verona and Regional Center for Osteoporosis, Verona, Italy.
Davide GattiRheumatology Unit, Department of Medicine, , University of Verona and Regional Center for Osteoporosis, Verona, Italy.
Maura RaveraDepartment of Nephrology and Dialysis, S. Martino Hospital, Genoa, Italy.
Luca Di LulloDepartment of Nephrology and Dialysis, Parodi-Delfino Hospital, Colleferro, Italy.
Antonio BellasiDepartment of Nephrology and Dialysis, S. Anna Hospital, ASST Lariana, Como, Italy.
Giuliano BrunoriSC Multizonale di Nefrologia e Dialisi, APSS, Trento, Italy.
Antonio PiccoliNephrology Unit, University of Padua, Padua, Italy.
Giovanni TripepiClinical Epidemiology and Physiopathology of Renal Diseases and Hypertension, CNR, Institute of Clinical Physiology, Reggio Calabria, Calabria, Italy.
Mario PlebaniLaboratory Medicine Unit, Department of Medicine, University of Padova, Padua, Italy.
University of Padua · ITIstituto di Fisiologia Clinica · ITUniversity of Verona · ITAzienda Socio Sanitaria Territoriale Lariana · ITColumbia University Irving Medical Center · USCTO Hospital · ITEnte Ospedaliero Ospedali Galliera · ITOspedale di Circolo di Busto Arsizio · ITOspedale Policlinico San Martino · ITSocietà Italiana di Nefrologia · ITUniversity of Cagliari · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsDiabetes mellitus is recognized as one of the major causes of end stage kidney disease. Bone Gla protein (BGP) is a vitamin K-dependent protein involved in bone mineralization and vascular calcifications (VC). Our goal was to characterize BGP and undercarboxylated BGP (ucBGP) in DM patients on HD, compared to HD patients without DM, and their association with vascular and bone disease.

methods387 HD patients from 18 dialysis centers in Italy. Associations of DM, levels of BGP, vitamin D and VC were evaluated. Time-to-event analysis for all-cause mortality was performed by the Kaplan-Meier.

resultsPatients with DM had lower levels of total BGP (139.00 vs. 202.50 mcg/L, p < 0.001), 25(OH)D (23.4 vs. 30.2 ng/ml, p < 0.001), and ucBGP (9.24 vs. 11.32 mcg/L, p = 0.022). In regression models, the geometric means of total BGP and ucBGP were 19% (p = 0.009) and 26% (p = 0.034) lower in diabetic patients. In univariate Cox regression analysis, DM patients had a higher risk of all-cause mortality (HR:1.83, 95% CI 1.13-2.96, p = 0.014). Adjustment for confounders confirmed the significant DM-mortality link. We included VC and warfarin into the Cox model, the DM-mortality link was no longer significant, suggesting a role of these risk factors as causal mediators leading to increased mortality in dialysis patients.

conclusionsHD patients have an increased mortality risk associated with DM. Furthermore, we found an association between DM and decreased BGP levels. Although our study does not support the notion that BGP levels act as mediator in the DM-mortality link, to our knowledge this is the first study in HD patients suggesting a potential protective role of BGP in the bone, endocrine and vascular pathway.

Indexed as

AgedDiabetes ComplicationsFemaleHumansItalyKaplan-Meier EstimateMaleMiddle AgedOsteocalcinProportional Hazards ModelsRenal DialysisRenal Insufficiency, ChronicRisk FactorsSpinal FracturesVascular CalcificationVitamin D25-hydroxyvitamin DBGLAP protein, humanOsteocalcinVitamin DBGPDiabetes mellitusHemodialysisVitamin K

Identifiers

PMID30759309
OpenAlexW2912595620

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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.