Value Assignment of Vitamin D Metabolites in Vitamin D Standardization Program Serum Samples
Karen W Phinney1, Johanna E Camara1, Susan S-C Tai1
1National Institute of Standards and Technology, Biomolecular Measurement Division and Chemical Sciences Division, Gaithersburg, MD 20899.
Journal of AOAC International
|June 18, 2017
Summary
Standardizing vitamin D measurements is crucial for optimal exposure. This study used two advanced methods to assign values to 50 serum samples, establishing a foundation for the Vitamin D Standardization Program.
Area of Science:
- Clinical Chemistry
- Analytical Chemistry
- Endocrinology
Background:
- Assay variability in 25-hydroxyvitamin D [25(OH)D] measurement hinders optimal vitamin D status assessment.
- Standardization of vitamin D measurements is essential for accurate clinical interpretation and public health guidance.
Purpose of the Study:
- To standardize the measurement of total 25-hydroxyvitamin D [25(OH)D] as part of the Vitamin D Standardization Program (VDSP).
- To assign accurate values to 50 serum samples using validated reference measurement procedures.
Main Methods:
- Utilized two isotope-dilution liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods.
- Employed methods recognized as reference measurement procedures (RMPs) by the Joint Committee for Traceability in Laboratory Medicine.
- Assigned values to 50 single-donor serum samples.
Main Results:
- Successfully assigned 25(OH)D values to 50 serum samples.
- Demonstrated the feasibility of using two RMPs for value assignment in a large sample set.
- Established a foundational set of characterized samples for the VDSP.
Conclusions:
- The use of two RMPs provides a robust approach for standardizing 25(OH)D measurements.
- This study represents a significant advancement in vitamin D measurement standardization.
- The characterized serum samples will support ongoing VDSP efforts and improve vitamin D testing accuracy.
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