Dimension EXL Vitamin D Total Assay

Dimension EXL Vitamin D Total Assay
 
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Siemens Healthineers now offers a LOCI® Vitamin D Total assay on the Dimension® EXL™ Integrated Chemistry Systems. This assay enables laboratories to provide highly accurate total 25(OH) vitamin D results (~100% D2 and D3) with a fast turnaround time. Vitamin D testing can now be consolidated with routine testing on a fully automated, high-throughput integrated chemistry system.
 

  • Provides excellent sensitivity for more-accurate differential diagnosis of vitamin D insufficiencies and improved patient care.
  • Delivers fast turnaround time—31 minutes to first result.
  • Offers good reagent and calibration stability for improved operational and labor efficiency with less hands-on time.
  • Allows workload consolidation of routine and specialized tests for increased productivity. 

 

Demand for vitamin D testing continues to grow, prompted by emerging research on the importance of vitamin D to wellness. Recent studies show that globally, over one billion people are vitamin D-deficient2, and deficiency rates have increased as people have limited their sun exposure due to the risk of skin cancer.

Vitamin D deficiency has long been associated with rickets in children and osteomalacia in adults, and long-term insufficiency of calcium and vitamin D leads to osteoporosis. However, in recent years, vitamin D has become an assay of general health status, and there have been multiple publications linking vitamin D deficiency to several disease states, such as cancer, cardiovascular, diabetes, and autoimmune diseases3.


Measurement of total vitamin D can aid in the correct interpretation of patients’ overall health status.

Assay Specifications

Assay SpecificationsDimension EXL LOCI Vitamin D Total Assay
Sample TypeSerum, Lithium Heparin Plasma, EDTA Plasma
Sample Volume8 µL
Assay Range5.0 – 150.0 ng/mL [12.5 – 375.0 nmol/L]
Limit of Quantitation5.0 ng/mL [12.5 nmol/L]
Calibration Interval7 days
Onboard Stability30 days
Time To First Result31 minutes

  

Download Specification sheet 0.3 MB

Vitamin D Standardization

Why Are Standardized Reference Materials Important?

Standardization of reference materials for in vitro diagnostic tests helps to harmonize results across test manufacturers and methods to improve the diagnosis, treatment, and prevention of disease. Reference standards serve as an anchor that can provide comparability across time and methods. Developing reference standards for assays is not a universal or easy procedure; success of any international reference material depends on that material being commutable across all manufacturers and methods.

Impact of the Lack of Standardization for Vitamin D

Without an internationally recognized, commutable vitamin D reference material, biases in slopes across methods and manufacturers can be observed. Scatter is apparent in assay comparisons between manufacturers as well as between laboratory-developed LC/MS/MS assays; this scatter may be due to differences in the way the different manufacturers’ systems measure vitamin D, varying vitamin D releasing processes, and heterophilic interferences.
Vitamin D standardization is necessary to create the anchor vitamin D values need, and it is important that laboratories and clinicians know how their vitamin D assay is standardized.

The Vitamin D Standardization Program (VDSP)

VDSP is an initiative of the NIH Office of Dietary Supplements (NIH ODS) and a collaboration with the National Institute of Standards and Technology (NIST), the CDC, and Ghent University.

  • VDSP, under the coordination of Christopher Sempos, PhD, NIH ODS, aims to standardize 25(OH)vitamin D measurement across methods and manufacturers.
  • The NIST Reference Measurement Procedure (RMP) is the primary reference method for the measurement of total 25(OH)vitamin D. This method separates out the 3-epi-25(OH)vitamin D3 from the 25(OH)vitamin D3, ensuring that the 25(OH)vitamin D3 is not overestimated.
  • A second method by Prof. Linda Thienpont, Ghent University, is also available. It is an ID-LC/MS/MS method for vitamin D in human serum that is traceable to NIST Standard SRM2972.4

CDC Hormone Standardization Program (HoSt)

Ongoing manufacturer certification for vitamin D standardization will be part of the CDC HoSt program, conducted by the CDC’s Clinical Chemistry Branch, Division of Laboratory Services, under the supervision of Hubert W. Vesper, PhD, Director, Clinical Standardization Programs, and Chief, Protein Biomarker Biomarker and Lipid Reference Laboratory. Previous HoSt program assays include testosterone and estradiol.
The CDC Standardization Program for vitamin D is a two-phase process:

  • First, assay manufacturers submit initial sample results for calibration to the standard.
  • Manufacturers then receive quarterly blinded challenges to verify and monitor stability of calibration over time.
  • The performance criteria are a mean bias of 5% and imprecision of 10%.
  • After participants pass four consecutive surveys, they are awarded a certification for a year.5 Renewal is an annual process.

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1CDC Vitamin D Standardization-Certification Program (VDSCP) --Total 25hydroxy Vitamin D Certified Procedures; 2017 Mar [cited 2017 Jun]. Available from: https://www.cdc.gov/labstandards/pdf/hs/CDC_Certified_Vitamin_D_Procedures.pdf

2Holick MF. Vitamin D deficiency. N Engl J Med. 2007;357(3):266-81.

3National Institutes of Health, Office of Dietary Supplements. Dietary supplemental fact sheet: vitamin D. Updated 11/13/2009. Accessed 08/17/2010.

4Scand J Clin Lab Invest. 2012;72(Suppl 243):41-49. 2

5http://www.cdc.gov/labstandards/hs.html.

The products/features (mentioned herein) are not commercially available in all countries. Due to regulatory reasons their future availability cannot be guaranteed. Please contact your local Siemens Healthineers organization for further details.