Biological variation of inflammatory and iron metabolism markers in high-endurance recreational athletes; are these markers useful for athlete monitoring?

Author:

Diaz-Garzon Jorge1ORCID,Itkonen Outi2,Aarsand Aasne K.34,Sandberg Sverre34,Coskun Abdurrahman5ORCID,Carobene Anna6,Jonker Niels7,Bartlett William A.8,Buño Antonio1,Fernandez-Calle Pilar1

Affiliation:

1. Laboratory Medicine Department , La Paz University Hospital , Madrid , Spain

2. Endocrinology and Metabolism Laboratory , Helsinki University Hospital , Helsinki , Finland

3. Department of Medical Biochemistry and Pharmacology, Norwegian Porphyria Centre , Haukeland University Hospital , Bergen , Norway

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

5. Department of Medical Biochemistry Atasehir, School of Medicine , Acibadem Mehmet Ali Aydınlar University , Istanbul , Türkiye

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

7. Certe, Wilhelmina Ziekenhuis Assen , Assen , The Netherlands

8. Undergraduate Teaching, School of Medicine , University of Dundee , Dundee , Scotland

Abstract

Abstract Objectives To deliver biological variation (BV) data for serum hepcidin, soluble transferrin receptor (sTfR), erythropoietin (EPO) and interleukin 6 (IL-6) in a population of well-characterized high-endurance athletes, and to evaluate the potential influence of exercise and health-related factors on the BV. Methods Thirty triathletes (15 females) were sampled monthly (11 months). All samples were analyzed in duplicate and BV estimates were delivered by Bayesian and ANOVA methods. A linear mixed model was applied to study the effect of factors related to exercise, health, and sampling intervals on the BV estimates. Results Within-subject BV estimates (CVI) were for hepcidin 51.9 % (95 % credibility interval 46.9–58.1), sTfR 10.3 % (8.8–12) and EPO 27.3 % (24.8–30.3). The mean concentrations were significantly different between sex, but CVI estimates were similar and not influenced by exercise, health-related factors, or sampling intervals. The data were homogeneously distributed for EPO but not for hepcidin or sTfR. IL-6 results were mostly below the limit of detection. Factors related to exercise, health, and sampling intervals did not influence the BV estimates. Conclusions This study provides, for the first time, BV data for EPO, derived from a cohort of well-characterized endurance athletes and indicates that EPO is a good candidate for athlete follow-up. The application of the Bayesian method to deliver BV data illustrates that for hepcidin and sTfR, BV data are heterogeneously distributed and using a mean BV estimate may not be appropriate when using BV data for laboratory and clinical applications.

Funder

Suomen kliinisen kemian yhdistys

Hospital La Paz Research Foundation

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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