European Biological Variation Study (EuBIVAS): within- and between-subject biological variation estimates for serum thyroid biomarkers based on weekly samplings from 91 healthy participants

Author:

Bottani Michela1,Aarsand Aasne K.23,Banfi Giuseppe14,Locatelli Massimo5,Coşkun Abdurrahman6,Díaz-Garzón Jorge78,Fernandez-Calle Pilar78,Sandberg Sverre239,Ceriotti Ferruccio10ORCID,Carobene Anna5

Affiliation:

1. IRCCS Istituto Ortopedico Galeazzi, Laboratory of Experimental Biochemistry & Molecular Biology , Milan , Italy

2. Department of Medical Biochemistry and Pharmacology , Haukeland University Hospital , Bergen , Norway

3. Norwegian Organization for Quality Improvement of Laboratory Examinations (Noklus), Haraldsplass Deaconess Hospital , Bergen , Norway

4. Vita-Salute San Raffaele University , Milan , Italy

5. Laboratory Medicine, IRCCS San Raffaele Scientific Institute , Milan , Italy

6. School of Medicine, Acibadem Mehmet Ali Aydınlar University , Istanbul , Turkey

7. Hospital Universitario La Paz , Madrid , Spain

8. Quality Analytical Commission of Spanish Society of Clinical Chemistry (SEQC) , Barcelona , Spain

9. Department of Global Public Health and Primary Care , University of Bergen , Bergen , Norway

10. Clinical Laboratory, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico , Milan , Italy

Abstract

Abstract Objectives Thyroid biomarkers are fundamental for the diagnosis of thyroid disorders and for the monitoring and treatment of patients with these diseases. The knowledge of biological variation (BV) is important to define analytical performance specifications (APS) and reference change values (RCV). The aim of this study was to deliver BV estimates for thyroid stimulating hormone (TSH), free thyroxine (FT4), free triiodothyronine (FT3), thyroglobulin (TG), and calcitonin (CT). Methods Analyses were performed on serum samples obtained from the European Biological Variation Study population (91 healthy individuals from six European laboratories; 21–69 years) on the Roche Cobas e801 at the San Raffaele Hospital (Milan, Italy). All samples from each individual were evaluated in duplicate within a single run. The BV estimates with 95% CIs were obtained by CV-ANOVA, after analysis of variance homogeneity and outliers. Results The within-subject (CV I ) BV estimates were for TSH 17.7%, FT3 5.0%, FT4 4.8%, TG 10.3, and CT 13.0%, all significantly lower than those reported in the literature. No significant differences were observed for BV estimates between men and women. Conclusions The availability of updated, in the case of CT not previously published, BV estimates for thyroid markers based on the large scale EuBIVAS study allows for refined APS and associated RCV applicable in the diagnosis and management of thyroid and related diseases.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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