Analytical bias in the measurement of serum 25-hydroxyvitamin D concentrations impairs assessment of vitamin D status in clinical and research settings
dc.contributor.author | Black, Lucinda | |
dc.contributor.author | Anderson, D. | |
dc.contributor.author | Clarke, M. | |
dc.contributor.author | Ponsonby, A.-L. | |
dc.contributor.author | Lucas, R. | |
dc.date.accessioned | 2017-01-30T15:29:27Z | |
dc.date.available | 2017-01-30T15:29:27Z | |
dc.date.created | 2016-04-28T19:30:18Z | |
dc.date.issued | 2015 | |
dc.identifier.citation | Black, L. and Anderson, D. and Clarke, M. and Ponsonby, A.-L. and Lucas, R. 2015. Analytical bias in the measurement of serum 25-hydroxyvitamin D concentrations impairs assessment of vitamin D status in clinical and research settings. PLoS One. 10 (8): Article ID e0135478. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/46832 | |
dc.identifier.doi | 10.1371/journal.pone.0135478 | |
dc.description.abstract |
Measured serum 25-hydroxyvitamin D concentrations vary depending on the type of assay used and the specific laboratory undertaking the analysis, impairing the accurate assessment of vitamin D status. We investigated differences in serum 25-hydroxyvitamin D concentrations measured at three laboratories (laboratories A and B using an assay based on liquid chromatography-tandem mass spectrometry and laboratory C using a DiaSorin Liaison assay), against a laboratory using an assay based on liquid chromatography-tandem mass spectrometry that is certified to the standard reference method developed by the National Institute of Standards and Technology and Ghent University (referred to as the ‘ certified laboratory ’ ). Separate aliquots from the same original serum sample for a subset of 50 participants from the Ausimmune Study were analysed at the four laboratories. Bland-Altman plots were used to visually check agreement between each laboratory against the certified laboratory. Compared with the certified laboratory, serum 25-hydroxyvitamin D concentrations were on average 12.4 nmol/L higher at laboratory A (95% limits of agreement: -17 .8,42.6); 12.8 nmol/L higher at laboratory B (95% limits of agreement: 0.8,24.8); and 10.6 nmol/L lower at laboratory C (95% limits of agreement: -48.4,27.1). The prevalence of vitamin D deficiency (defined here as 25-hydroxyvitamin D < 50 nmol/L) was 24%, 16%, 12% and 41% at the certified laboratory, and laboratories A, B, and C, respectively. Our results demonstrate considerable differences in the measurement of 25-hydroxyvitamin D concentrations compared with a certified laboratory, even between laboratories using assays based on liquid chromatography-tandem mass spectrometry, which is often considered the gold-standard assay. To ensure accurate and reliable measurement of serum 25-hydroxyvitamin D concentrations, all laboratories should use an accuracy-based quality assurance system and, ideally, comply with international standardisation efforts | |
dc.publisher | Public Library of Science | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.title | Analytical bias in the measurement of serum 25-hydroxyvitamin D concentrations impairs assessment of vitamin D status in clinical and research settings | |
dc.type | Journal Article | |
dcterms.source.volume | 10 | |
dcterms.source.number | 8 | |
dcterms.source.startPage | 1 | |
dcterms.source.endPage | 14 | |
dcterms.source.issn | 1932-6203 | |
dcterms.source.title | PLoS One | |
curtin.department | School of Public Health | |
curtin.accessStatus | Open access |