The European Biological Variation Study (EuBIVAS): Biological Variation Data for Coagulation Markers Estimated by a Bayesian Model

• Published in: Clinical chemistry (Baltimore, Md.) Vol. 67; no. 9; pp. 1259 - 1270
• Main Authors: Aarsand, Aasne K, Kristoffersen, Ann Helen, Sandberg, Sverre, Støve, Bård, Coşkun, Abdurrahman, Fernandez-Calle, Pilar, Díaz-Garzón, Jorge, Guerra, Elena, Ceriotti, Ferruccio, Jonker, Niels, Røraas, Thomas, Carobene, Anna
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 01.09.2021
• Subjects: Antithrombin; Bayes Theorem; Bayesian analysis; Biological variation; Biomarkers; Coagulation; Coagulation factors; Dimers; Estimates; Female; Fibrinogen; Fibrinogen - metabolism; Humans; Male; Markers; Men; Partial Thromboplastin Time; Population studies; Protein C; Protein S; Proteins; Prothrombin; Prothrombin Time; Subgroups; Thromboplastin; Variation; Women; analytical performance specification; biological variation; Bayesian model; reference change value; within-subject biological variation
• ISSN: 0009-9147; 1530-8561; 1530-8561
• DOI: 10.1093/clinchem/hvab100

Abstract Background For biological variation (BV) data to be safely used, data must be reliable and relevant to the population in which they are applied. We used samples from the European Biological Variation Study (EuBIVAS) to determine BV of coagulation markers by a Bayesian model robust to extreme observations and used the derived within-participant BV estimates [CVP(i)] to assess the applicability of the BV estimates in clinical practice. Method Plasma samples were drawn from 92 healthy individuals for 10 consecutive weeks at 6 European laboratories and analyzed in duplicate for activated partial thromboplastin time (APTT), prothrombin time (PT), fibrinogen, D-dimer, antithrombin (AT), protein C, protein S free, and factor VIII (FVIII). A Bayesian model with Student t likelihoods for samples and replicates was applied to derive CVP(i) and predicted BV estimates with 95% credibility intervals. Results For all markers except D-dimer, CVP(i) were homogeneously distributed in the overall study population or in subgroups. Mean within-subject estimates (CVI) were <5% for APTT, PT, AT, and protein S free, <10% for protein C and FVIII, and <12% for fibrinogen. For APTT, protein C, and protein S free, estimates were significantly lower in men than in women ≤50 years. Conclusion For most coagulation markers, a common CVI estimate for men and women is applicable, whereas for APTT, protein C, and protein S free, sex-specific reference change values should be applied. The use of a Bayesian model to deliver individual CVP(i) allows for improved interpretation and application of the data.