Abstract

Background Several studies have investigated copeptin as a prognostic marker of different acute diseases and as a diagnostic marker in disorders of water and salt homeostasis. However, no data of the normal circadian rhythm of copeptin in healthy subjects are available. Aim To investigate the circadian rhythm of copeptin in healthy subjects under standardized conditions. Methods 19 healthy volunteers aged 18 to 53 years, male and female, were studied in a prospective observational study. In all 19 participants, blood samples for copeptin were taken in regular intervals of 30 minutes for 24 hours after a fasting period of minimum 8 hours. Results The mean values of copeptin showed a circadian rhythm, similar to that described for AVP release, with a trend towards higher levels (5.9 ± 1 pmol/L) at night and early morning between 4 am and 6 am and lowest levels (2.3 ± 0.2 pmol/L) in the late afternoon between 5 pm and 7 pm. This finding was only observed in individuals with initial higher copeptin levels, whereas in individuals with lower basal copeptin levels no circadian rhythm was observed. Conclusion There is evidence for a circadian rhythm in copeptin release during 24 hours, however, of minor extent. These findings suggest that copeptin levels can be determined irrespectively of the time of the day.

Highlights

  • Copeptin, a 39-amino acid glycopeptide comprising the Cterminal part of the Arginine vasopressin AUC (AVP) precursor (CT-proAVP (Arginine Vasopressin)), was found to be a stable and sensitive marker for AVP release and seems to be released stoichiometrically together with AVP [1]

  • The main finding of our study is that copeptin shows a circadian rhythm similar to that described for AVP, but with a later peak for Cmax and later nadir for Cmin

  • This finding might be due to the longer half-life of copeptin of around 86 minutes compared to the shorter half-life of AVP with 44 minutes or less (13; own data submitted)

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Summary

Introduction

A 39-amino acid glycopeptide comprising the Cterminal part of the AVP precursor (CT-proAVP (Arginine Vasopressin)), was found to be a stable and sensitive marker for AVP release and seems to be released stoichiometrically together with AVP [1]. The mean values of copeptin showed a circadian rhythm, similar to that described for AVP release, with a trend towards higher levels (5.9 ± 1 pmol/L) at night and early morning between 4 am and 6 am and lowest levels (2.3 ± 0.2 pmol/L) in the late afternoon between 5 pm and 7 pm. This finding was only observed in individuals with initial higher copeptin levels, whereas in individuals with lower basal copeptin levels no circadian rhythm was observed. These findings suggest that copeptin levels can be determined irrespectively of the time of the day

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