PTH determination in hemodialyzed patients-A laboratory perspective
Etienne Cavalier1,2,3, Jean-Claude Souberbielle4, Pierre Delanaye5
1Department of Clinical chemistry, CHU de Liège, University of Liège, Liège, Belgium.
Insights
Measuring parathyroid hormone (PTH) in chronic kidney disease (CKD) patients is complex due to issues with PTH stability, assay standardization, and potential in vivo oxidation, impacting accurate CKD-MBD monitoring.
Area of Science:
- Biochemistry
- Nephrology
- Endocrinology
Background:
- Parathyroid hormone (PTH) is crucial for bone remodeling in Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD).
- Serum PTH levels are routinely monitored in patients with chronic kidney disease (CKD).
Discussion:
- PTH stability is a significant concern, with degradation occurring during improper storage.
- Immunoassays may detect biologically active PTH alongside inactive fragments and oxidized forms.
- Lack of assay standardization leads to variability and confusion in patient monitoring.
Key Insights:
- Assay variability complicates consistent patient management across different healthcare settings.
- Established reference ranges, particularly upper limits, are often inadequately defined.
- In vivo oxidation of PTH can lead to overestimation of biologically active hormone levels.
Outlook:
- Standardization of PTH assays is essential for reliable CKD-MBD management.
- Further research is needed to address PTH stability and oxidation issues.
- Improved measurement techniques will enhance patient care and therapeutic decisions in CKD.
Abstract:
Parathyroid hormone (PTH) is a key player of bone remodelling in patients suffering from Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD). Serum PTH concentrations are thus frequently measured in CKD patients. Nevertheless, this determination is far from simple. PTH stability can be an issue and degradation of the peptide can be important if storage is not properly done. Biologically active PTH circulates together with fragments, which can be detected by some immunoassays. There is, up to now, no standardization of the assays available on the market, which can lead to some confusion when patients are followed with different methods. The upper end of the reference ranges provided by some manufacturers have not been properly established and are sometimes far too high. Finally, PTH can be oxidized in vivo and thus become inactive, while still quantified by immunoassays. In this Editorial, we will try to highlight some of these issues on PTH measurement.
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