Key result
Hemodialysis raises plasma copeptin ~15%, driven by falling blood volume and blood pressure.
Why the study?
It is unknown what drives elevated plasma copeptin levels in hemodialysis patients and whether physiological stimuli for copeptin release are operational in this population.
Do volume stimuli (MAP and blood volume) or osmotic stimuli drive changes in plasma copeptin levels during hemodialysis in stable hemodialysis patients?
Observational (n=108)
Yes
Do volume stimuli (MAP and blood volume) or osmotic stimuli drive changes in plasma copeptin levels during hemodialysis in stable hemodialysis patients?
Absolute Event Rate: 163% vs 141.5%
p-value: p=<0.01
In hemodialysis patients, plasma copeptin levels are elevated and increase further during dialysis, driven primarily by volume stimuli (decreases in MAP and blood volume) rather than osmotic stimuli.
Copeptin rises during hemodialysis may reflect volume/MAP changes rather than osmolality; leaves open its role as a hemodynamic marker pending prospective validation.
OBJECTIVES: Plasma levels of copeptin, a surrogate marker for the vasoconstrictor hormone arginine vasopressin (AVP), are increased in hemodialysis patients. Presently, it is unknown what drives copeptin levels in hemodialysis patients. We investigated whether the established physiological stimuli for copeptin release, i.e. plasma osmolality, blood volume and mean arterial pressure (MAP), are operational in hemodialysis patients. METHODS: One hundred and eight prevalent, stable hemodialysis patients on a thrice-weekly dialysis schedule were studied during hemodialysis with constant ultrafiltration rate and dialysate conductivity in this observational study. Plasma levels of copeptin, sodium, MAP, and blood volume were measured before, during and after hemodialysis. Multivariate analysis was used to determine the association between copeptin (dependent variable) and the physiological stimuli plasma sodium, MAP, excess weight as well as NT-pro-BNP immediately prior to dialysis and between copeptin and changes of plasma sodium, MAP and blood volume with correction for age, sex and diabetes during dialysis treatment. RESULTS: Patients were 63 ± 15.6 years old and 65% were male. Median dialysis vintage was 1.6 years (IQR 0.7-4.0). Twenty-three percent of the patients had diabetes and 82% had hypertension. Median predialysis copeptin levels were 141.5 pmol/L (IQR 91.0-244.8 pmol/L). Neither predialysis plasma sodium levels, nor NT-proBNP levels, nor MAP were associated with predialysis copeptin levels. During hemodialysis, copeptin levels rose significantly (p<0.01) to 163.0 pmol/L (96.0-296.0 pmol/L). Decreases in blood volume and MAP were associated with increases in copeptin levels during dialysis, whereas there was no significant association between the change in plasma sodium levels and the change in copeptin levels. CONCLUSIONS: Plasma copeptin levels are elevated predialysis and increase further during hemodialysis. Volume stimuli, i.e. decreases in MAP and blood volume, rather than osmotic stimuli, are associated with change in copeptin levels during hemodialysis.
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Ettema et al. (2015) conducted an observational in End-stage renal disease on hemodialysis (n=108). Hemodialysis vs. Predialysis baseline was evaluated on Change in plasma copeptin levels (p=<0.01). Plasma copeptin levels increased significantly during hemodialysis from a median of 141.5 to 163.0 pmol/L (p<0.01), driven by intradialytic decreases in blood volume and mean arterial pressure.
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