European Biological Variation Study (EuBIVAS): Within- and Between-Subject Biological Variation Data for 15 Frequently Measured Proteins.


Journal

Clinical chemistry
ISSN: 1530-8561
Titre abrégé: Clin Chem
Pays: England
ID NLM: 9421549

Informations de publication

Date de publication:
08 2019
Historique:
received: 14 03 2019
accepted: 13 05 2019
pubmed: 7 6 2019
medline: 17 4 2020
entrez: 8 6 2019
Statut: ppublish

Résumé

The European Biological Variation Study (EuBIVAS) was established to deliver rigorously determined data for biological variation (BV). Here, EuBIVAS-based BV estimates are provided for α Serum samples from weekly blood samplings of 91 healthy study participants (38 males and 53 females, ages 21-69 years old) over 10 consecutive weeks in 6 European laboratories were stored at -80 °C before duplicate analysis on a Roche Cobas c702. Outlier and variance homogeneity analyses were performed followed by CV-ANOVA on trend-corrected data if relevant, to determine BV and analytical variation estimates with CI and the associated RCV. For the acute phase proteins, several participants experienced mild inflammatory episodes during the study, requiring exclusion of 7% of the 25290 results. Within-subject BV (CV In addition to new BV estimates for sTfR, this EuBIVAS substudy generated more demanding APS for frequently requested plasma specific proteins. APS for CRP should not be calculated from BV data except when CRP is used as a risk factor for cardiovascular disease.

Sections du résumé

BACKGROUND
The European Biological Variation Study (EuBIVAS) was established to deliver rigorously determined data for biological variation (BV). Here, EuBIVAS-based BV estimates are provided for α
METHOD
Serum samples from weekly blood samplings of 91 healthy study participants (38 males and 53 females, ages 21-69 years old) over 10 consecutive weeks in 6 European laboratories were stored at -80 °C before duplicate analysis on a Roche Cobas c702. Outlier and variance homogeneity analyses were performed followed by CV-ANOVA on trend-corrected data if relevant, to determine BV and analytical variation estimates with CI and the associated RCV.
RESULTS
For the acute phase proteins, several participants experienced mild inflammatory episodes during the study, requiring exclusion of 7% of the 25290 results. Within-subject BV (CV
CONCLUSIONS
In addition to new BV estimates for sTfR, this EuBIVAS substudy generated more demanding APS for frequently requested plasma specific proteins. APS for CRP should not be calculated from BV data except when CRP is used as a risk factor for cardiovascular disease.

Identifiants

pubmed: 31171528
pii: clinchem.2019.304618
doi: 10.1373/clinchem.2019.304618
doi:

Substances chimiques

Acute-Phase Proteins 0
Blood Proteins 0
Cystatin C 0
Immunoglobulins 0
Receptors, Transferrin 0
Serum Albumin 0
Transferrin 0
C-Reactive Protein 9007-41-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1031-1041

Informations de copyright

© 2019 American Association for Clinical Chemistry.

Auteurs

Anna Carobene (A)

Laboratory Medicine, Ospedale San Raffaele, Milan, Italy.
Biological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.

Aasne K Aarsand (AK)

Biological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.
Department of Medical Biochemistry and Clinical Pharmacology, Haukeland University Hospital, Bergen, Norway.
Norwegian Quality Improvement of Laboratory Examinations (Noklus), Haraldsplass Deaconess Hospital, Bergen, Norway.

Elena Guerra (E)

Laboratory Medicine, Ospedale San Raffaele, Milan, Italy.

William A Bartlett (WA)

Biological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.
Blood Sciences, Ninewells Hospital and Medical School, Scotland, UK.

Abdurrahman Coşkun (A)

Biological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.
Acibadem Mehmet Ali Aydinlar University, School of Medicine, Atasehir, Istanbul, Turkey.

Jorge Díaz-Garzón (J)

Biological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.
Hospital Universitario La Paz, Madrid, Spain, and Quality Analytical Commission of Spanish Society of Clinical Chemistry (SEQC).

Pilar Fernandez-Calle (P)

Biological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.
Hospital Universitario La Paz, Madrid, Spain, and Quality Analytical Commission of Spanish Society of Clinical Chemistry (SEQC).

Niels Jonker (N)

Biological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.
Certe, Wilhelmina Ziekenhuis Assen, Assen, the Netherlands.

Massimo Locatelli (M)

Laboratory Medicine, Ospedale San Raffaele, Milan, Italy.

Sverre Sandberg (S)

Biological Variation Working Group, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy.
Department of Medical Biochemistry and Clinical Pharmacology, Haukeland University Hospital, Bergen, Norway.
Norwegian Quality Improvement of Laboratory Examinations (Noklus), Haraldsplass Deaconess Hospital, Bergen, Norway.
Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.

Ferruccio Ceriotti (F)

Clinical Laboratory, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy. ferruccio.ceriotti@policlinico.mi.it.

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Classifications MeSH