Literature DB >> 34750644

Assessment of serum total 25-hydroxyvitamin D assays for Vitamin D External Quality Assessment Scheme (DEQAS) materials distributed at ambient and frozen conditions.

Christopher T Sempos1,2, Emma L Williams3, Graham D Carter3, Julia Jones3, Johanna E Camara4, Carolyn Q Burdette4, Grace Hahm4, Federica Nalin4, David L Duewer4, Adam J Kuszak1, Joyce Merkel1, Andrew N Hoofnagle5, Pierre Lukas6, Étienne Cavalier6, Ramón A Durazo-Arvizu7, Peter M Crump8, Christian Popp9, Christian Beckert9, Jan Schultess9, Glen Van Slooten10, Carole Tourneur11, Camille Pease11, Ravi Kaul12, Alfredo Villarreal12, Fiona Ivison13, Ralf Fischer14, Jody M W van den Ouweland15, Chung S Ho16, Emmett W K Law16, Jean-Nicolas Simard17, Renaud Gonthier17, Brett Holmquist18, Marcelo Cidade Batista19, Sarah Meadows20,21, Lorna Cox20,21, Eugene Jansen22, Dilshad Ahmed Khan23, Kimberly Robyak24, Michael H Creer24, Mark Kilbane25, Patrick J Twomey25, James Freeman26, Neil Parker26, Jinyun Yuan27, Robert Fitzgerald28, Sohail Mushtaq29, Michael W Clarke30, Norma Breen31, Christine Simpson32, Stephen A Wise33,34.   

Abstract

The Vitamin D External Quality Assessment Scheme (DEQAS) distributes human serum samples four times per year to over 1000 participants worldwide for the determination of total serum 25-hydroxyvitamin D [25(OH)D)]. These samples are stored at -40 °C prior to distribution and the participants are instructed to store the samples frozen at -20 °C or lower after receipt; however, the samples are shipped to participants at ambient conditions (i.e., no temperature control). To address the question of whether shipment at ambient conditions is sufficient for reliable performance of various 25(OH)D assays, the equivalence of DEQAS human serum samples shipped under frozen and ambient conditions was assessed. As part of a Vitamin D Standardization Program (VDSP) commutability study, two sets of the same nine DEQAS samples were shipped to participants at ambient temperature and frozen on dry ice. Twenty-eight laboratories participated in this study and provided 34 sets of results for the measurement of 25(OH)D using 20 ligand binding assays and 14 liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods. Equivalence of the assay response for the frozen versus ambient DEQAS samples for each assay was evaluated using multi-level modeling, paired t-tests including a false discovery rate (FDR) approach, and ordinary least squares linear regression analysis of frozen versus ambient results. Using the paired t-test and confirmed by FDR testing, differences in the results for the ambient and frozen samples were found to be statistically significant at p < 0.05 for four assays (DiaSorin, DIAsource, Siemens, and SNIBE prototype). For all 14 LC-MS/MS assays, the differences in the results for the ambient- and frozen-shipped samples were not found to be significant at p < 0.05 indicating that these analytes were stable during shipment at ambient conditions. Even though assay results have been shown to vary considerably among different 25(OH)D assays in other studies, the results of this study also indicate that sample handling/transport conditions may influence 25(OH)D assay response for several assays.
© 2021. This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply.

Entities:  

Keywords:  25-Hydroxyvitamin D2; 25-Hydroxyvitamin D3; Ligand binding assay; Liquid chromatography–tandem mass spectrometry (LC–MS/MS); Total 25-hydroxyvitamin D; Vitamin D External Quality Assessment Scheme (DEQAS)

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Substances:

Year:  2021        PMID: 34750644     DOI: 10.1007/s00216-021-03742-5

Source DB:  PubMed          Journal:  Anal Bioanal Chem        ISSN: 1618-2642            Impact factor:   4.142


  9 in total

1.  Candidate Reference Measurement Procedure for the Determination of (24R),25-Dihydroxyvitamin D3 in Human Serum Using Isotope-Dilution Liquid Chromatography-Tandem Mass Spectrometry.

Authors:  Susan S-C Tai; Michael A Nelson
Journal:  Anal Chem       Date:  2015-07-24       Impact factor: 6.986

Review 2.  Hydroxyvitamin D assays: An historical perspective from DEQAS.

Authors:  G D Carter; J Berry; R Durazo-Arvizu; E Gunter; G Jones; J Jones; H L J Makin; P Pattni; C T Sempos; P Twomey; E L Williams; S A Wise
Journal:  J Steroid Biochem Mol Biol       Date:  2017-07-20       Impact factor: 4.292

3.  Accuracy-Based Vitamin D Survey: Six Years of Quality Improvement Guided by Proficiency Testing.

Authors:  Patrick Erdman; Darryl E Palmer-Toy; Gary Horowitz; Andrew Hoofnagle
Journal:  Arch Pathol Lab Med       Date:  2019-05-22       Impact factor: 5.534

4.  Establishing an Accuracy Basis for the Vitamin D External Quality Assessment Scheme (DEQAS).

Authors:  Carolyn Q Burdette; Johanna E Camara; Federica Nalin; Jeanita Pritchett; Lane C Sander; Graham D Carter; Julia Jones; Joseph M Betz; Christopher T Sempos; Stephen A Wise
Journal:  J AOAC Int       Date:  2017-08-29       Impact factor: 1.913

5.  A candidate reference measurement procedure for quantifying serum concentrations of 25-hydroxyvitamin D₃ and 25-hydroxyvitamin D₂ using isotope-dilution liquid chromatography-tandem mass spectrometry.

Authors:  Ekaterina M Mineva; Rosemary L Schleicher; Madhulika Chaudhary-Webb; Khin L Maw; Julianne C Botelho; Hubert W Vesper; Christine M Pfeiffer
Journal:  Anal Bioanal Chem       Date:  2015-05-13       Impact factor: 4.142

6.  Development of a candidate reference measurement procedure for the determination of 25-hydroxyvitamin D3 and 25-hydroxyvitamin D2 in human serum using isotope-dilution liquid chromatography-tandem mass spectrometry.

Authors:  Susan S-C Tai; Mary Bedner; Karen W Phinney
Journal:  Anal Chem       Date:  2010-03-01       Impact factor: 6.986

7.  Role of the National Institute of Standards and Technology (NIST) in Support of the Vitamin D Initiative of the National Institutes of Health, Office of Dietary Supplements.

Authors:  Stephen A Wise; Susan S-C Tai; Carolyn Q Burdette; Johanna E Camara; Mary Bedner; Katrice A Lippa; Michael A Nelson; Federica Nalin; Karen W Phinney; Lane C Sander; Joseph M Betz; Christopher T Sempos; Paul M Coates
Journal:  J AOAC Int       Date:  2017-09-01       Impact factor: 1.913

8.  Vitamin D Standardization Program (VDSP) intralaboratory study for the assessment of 25-hydroxyvitamin D assay variability and bias.

Authors:  Stephen A Wise; Johanna E Camara; Christopher T Sempos; Pierre Lukas; Caroline Le Goff; Stephanie Peeters; Carolyn Q Burdette; Federica Nalin; Grace Hahm; Ramón A Durazo-Arvizu; Adam J Kuszak; Joyce Merkel; Étienne Cavalier
Journal:  J Steroid Biochem Mol Biol       Date:  2021-05-16       Impact factor: 5.011

9.  Assessment of serum total 25-hydroxyvitamin D assay commutability of Standard Reference Materials and College of American Pathologists Accuracy-Based Vitamin D (ABVD) Scheme and Vitamin D External Quality Assessment Scheme (DEQAS) materials: Vitamin D Standardization Program (VDSP) Commutability Study 2.

Authors:  Johanna E Camara; Stephen A Wise; Andrew N Hoofnagle; Emma L Williams; Graham D Carter; Julia Jones; Carolyn Q Burdette; Grace Hahm; Federica Nalin; Adam J Kuszak; Joyce Merkel; Ramón A Durazo-Arvizu; Pierre Lukas; Étienne Cavalier; Christian Popp; Christian Beckert; Jan Schultess; Glen Van Slooten; Carole Tourneur; Camille Pease; Ravi Kaul; Alfredo Villarreal; Fiona Ivison; Ralf Fischer; Jody M W van den Ouweland; Chung S Ho; Emmett W K Law; Jean-Nicolas Simard; Renaud Gonthier; Brett Holmquist; Marcelo Cidade Batista; Heather Pham; Alex Bennett; Sarah Meadows; Lorna Cox; Eugene Jansen; Dilshad Ahmed Khan; Kimberly Robyak; Michael H Creer; Mark Kilbane; Patrick J Twomey; James Freeman; Neil Parker; Jinyun Yuan; Robert Fitzgerald; Sohail Mushtaq; Michael W Clarke; Norma Breen; Christine Simpson; Christopher T Sempos
Journal:  Anal Bioanal Chem       Date:  2021-06-28       Impact factor: 4.478

  9 in total

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