Related Experiment Video
Updated: Dec 13, 2025

A Semi-Automated and Reproducible Biological-Based Method to Quantify Calcium Deposition In Vitro
Published on: June 2, 2022
Intradialytic Calcium Kinetics and Cardiovascular Disease in Chronic Hemodialysis Patients
Markus Pirklbauer1, Lisa Fuchs2, Ramona Heiss2
1Department of Internal Medicine IV - Nephrology and Hypertension, Medical University Innsbruck, Innsbruck, Austria, markus.pirklbauer@i-med.ac.at.
Insights
Intradialytic calcium buffering plays a role in hemodialysis (HD) patients, influencing cardiovascular risk. Understanding intradialytic calcium kinetics may help assess cardiovascular disease burden in this population.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Biochemistry
Background:
- Calcium loading is linked to cardiovascular risk in hemodialysis (HD) patients.
- The contribution of intradialytic calcium buffering to cardiovascular disease burden in HD patients requires further investigation.
Purpose of the Study:
- To evaluate intradialytic calcium kinetics in chronic HD patients.
- To assess the relationship between intradialytic calcium buffering, cardiovascular parameters, and biomarkers.
Main Methods:
- Cross-sectional observational study of 40 chronic HD patients.
- Measurement of dialysate-sided ionized calcium mass balance (iCaMB), calcium buffer capacity, and serum calcium changes during HD.
- Assessment of aortic pulse wave velocity, serum osteocalcin, cardiovascular disease, and diabetes.
Main Results:
- Mean intradialytic calcium buffer capacity was 73%.
- Higher serum calcium increase (∆iCa) was associated with coronary heart disease.
- Intradialytic calcium buffer capacity correlated with undercarboxylated osteocalcin.
Conclusions:
- Clinical evidence supports a role for intradialytic calcium regulation and osteocalcin as a biomarker.
- Further prospective trials are warranted to evaluate the prognostic potential of intradialytic calcium kinetics.
Background/Objective:
Calcium loading has been associated with cardiovascular risk in hemodialysis (HD) patients. However, it remains to be elucidated whether alterations of intradialytic calcium buffering add to the increased cardiovascular disease burden in this high-risk population.
Methods:
Intradialytic calcium kinetics was evaluated in a cross-sectional observational study by measuring dialysate-sided ionized calcium mass balance (iCaMB), calcium buffer capacity, and change in serum calcium levels in 40 chronic HD patients during a routine HD session. A dialysate calcium of 3.5 mEq/L was used to adequately challenge calcium buffer mechanisms. Aortic pulse wave velocity and serum osteocalcin levels were measured prior to the HD session. Presence of cardiovascular disease and diabetes was assessed.
Results:
The mean dialysate-sided iCaMB, extracellular fluid ionized calcium mass gain, and buffered ionized calcium mass were 469 (±154), 111 (±49), and 358 (±145) mg/HD, respectively. The mean ionized serum calcium increase (∆iCa) was 0.42 (±0.14) mEq/L per HD. The mean intradialytic calcium buffer capacity was 73 (±18)%. Multivariate regression analysis revealed significant independent association of (1) iCaMB with the dialysate-to-blood calcium gradient at HD start and (2) intradialytic calcium buffer capacity with undercarboxylated osteocalcin. The presence of coronary heart disease was associated with higher ∆iCa but not iCaMB in the multivariate model.
Conclusions:
In line with our proof-of-concept study, we provide clinical evidence for a rapidly accessible and exchangeable calcium pool involved in intradialytic calcium regulation and for the role of osteocalcin as a potential biomarker. Our findings argue for evaluating the prognostic potential of intradialytic calcium kinetics in prospective clinical trials.
Related Concept Videos
Chronic Kidney Disease II: Clinical Manifestations
Chronic Kidney Disease III: Interprofessional Care
Chronic Kidney Disease IV: Nursing Management
Hemodialysis II: Procedure and Complications
Skeleton and Calcium Homeostasis
Hemodialysis III: Nursing Management

