Evidence map›Paper›PMID 32270253›Full record

ArticleOsteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA2020

European Biological Variation Study (EuBIVAS): within- and between-subject biological variation estimates of β-isomerized C-terminal telopeptide of type I collagen (β-CTX), N-terminal propeptide of type I collagen (PINP), osteocalcin, intact fibroblast growth factor 23 and uncarboxylated-unphosphorylated matrix-Gla protein-a cooperation between the EFLM Working Group on Biological Variation and the International Osteoporosis Foundation-International Federation of Clinical Chemistry Committee on Bone Metabolism.

E Cavalier, P Lukas, M Bottani, A K Aarsand, F Ceriotti, A Coşkun, J Díaz-Garzón, P Fernàndez-Calle, E Guerra, M Locatelli and 3 more

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Article in Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Advances in laboratory medicine · 2024
    Article
  9. Clinical use of bone markers: a challenge to variability.Advances in laboratory medicine · 2024
    Article
  10. Biological variation estimates of Alzheimer's disease plasma biomarkers in healthy individuals.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  11. Article
  12. Broad application prospects of bone turnover markers in pediatrics.Journal of clinical laboratory analysis · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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 7 institutions in 6 countries.

E CavalierDepartment of Clinical Chemistry, University of Liège, CHU de Liège, 4000, Liège, Belgium. Etienne.cavalier@chuliege.be.ORCID http://orcid.org/0000-0003-0947-2226
P LukasDepartment of Clinical Chemistry, University of Liège, CHU de Liège, 4000, Liège, Belgium.
M BottaniIRCCS Istituto Ortopedico Galeazzi, Laboratory of Experimental Biochemistry & Molecular Biology, Milan, Italy.
A K AarsandDepartment of Medical Biochemistry and Pharmacology, Haukeland University Hospital, Bergen, Norway.
F CeriottiClinical Laboratory, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.
A CoşkunBiological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.
J Díaz-GarzónBiological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.
P Fernàndez-CalleBiological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.
E GuerraLaboratory Medicine, Ospedale San Raffaele, Milan, Italy.
M LocatelliLaboratory Medicine, Ospedale San Raffaele, Milan, Italy.
S SandbergDepartment of Medical Biochemistry and Pharmacology, Haukeland University Hospital, Bergen, Norway.
A CarobeneBiological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.
European Federation of Clinical Chemistry and Laboratory Medicine Working Group on Biological Variation and IOF-IFCC Committee on Bone Metabolism
European School of Molecular Medicine · ITHaukeland University Hospital · NOHospital Universitario La Paz · ESIRCCS Ospedale San Raffaele · ITUniversity of Liège · BEFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITIstituto Ortopedico Galeazzi · IT

Funding

Department of Health 10/33/04Medical Research Council G0400491Medical Research Council MC_U147585819Medical Research Council MC_U147585824Medical Research Council MC_U147585827Medical Research Council MC_UP_A620_1014Medical Research Council MC_UP_A620_1015Medical Research Council MC_UU_12011/1Medical Research Council MC_UU_12011/2
6 · The paper itself

Abstract

We have calculated the biological variation (BV) of different bone metabolism biomarkers on a large, well-described cohort of subjects. BV is important to calculate reference change value (or least significant change) which allows evaluating if the difference observed between two consecutive measurements in a patient is biologically significant or not.

introductionWithin-subject (CV

methodsIn the EuBIVAS, 91 subjects were recruited from six European laboratories. Fasting blood samples were obtained weekly for ten consecutive weeks. The samples were run in duplicate on IDS iSYS or DiaSorin Liaison instruments. The results were subjected to outlier and variance homogeneity analysis before CV-ANOVA was used to obtain the BV estimates.

resultsWe found no effect of gender upon the CV

conclusionsThe EuBIVAS has provided updated BV estimates for bone markers, including iFGF23, which have not been previously published, facilitating the improved follow-up of patients being treated for metabolic bone disease.

Indexed as

Biological Variation, PopulationBiomarkersCollagen Type IOsteoporosisalpha-GalactosidaseChemistry, ClinicalFibroblast Growth Factor-23Fibroblast Growth FactorsHumansOsteocalcinPeptidesalpha-GalactosidaseBiomarkersCollagen Type Icollagen type I trimeric cross-linked peptideFGF23 protein, humanFibroblast Growth Factor-23Fibroblast Growth FactorsGLA protein, humanOsteocalcinPeptidesBiological variationBone markersCTXFGF23MGPOsteocalcinPINPReference change value

Identifiers

PMID32270253
OpenAlexW3016041195

What OpenQuestion holds

Textmetadata
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.