<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wise SA</submitter><funding>Intramural NIH HHS</funding><funding>National Institutes of Health Office of the Director</funding><pagination>105917</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8403635</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>212</volume><pubmed_abstract>An intralaboratory study assessing assay variability and bias for determination of serum total 25-hydroxyvitamin D [25(OH)D] was conducted by the Vitamin D Standardization Program (VDSP). Thirteen assays for serum total 25(OH)D were evaluated in a single laboratory including 11 unique immunoassays and one liquid chromatography - tandem mass spectrometry (LC-MS/MS) assay. Fifty single-donor serum samples, including eight samples with high concentrations of 25(OH)D&lt;sub>2&lt;/sub> (> 30 nmol/L), were assigned target values for 25(OH)D&lt;sub>2&lt;/sub> and 25(OH)D&lt;sub>3&lt;/sub> using reference measurement procedures (RMP). Using four replicate measurements for each sample, the mean total percent coefficient of variation (%CV) and mean % bias from the target values were determined for each assay using th</pubmed_abstract><journal>The Journal of steroid biochemistry and molecular biology</journal><pubmed_title>Vitamin D Standardization Program (VDSP) intralaboratory study for the assessment of 25-hydroxyvitamin D assay variability and bias.</pubmed_title><pmcid>PMC8403635</pmcid><funding_grant_id>Z99 OD999999</funding_grant_id><pubmed_authors>Camara JE</pubmed_authors><pubmed_authors>Hahm G</pubmed_authors><pubmed_authors>Sempos CT</pubmed_authors><pubmed_authors>Wise SA</pubmed_authors><pubmed_authors>Burdette CQ</pubmed_authors><pubmed_authors>Cavalier E</pubmed_authors><pubmed_authors>Merkel J</pubmed_authors><pubmed_authors>Nalin F</pubmed_authors><pubmed_authors>Peeters S</pubmed_authors><pubmed_authors>Le Goff C</pubmed_authors><pubmed_authors>Durazo-Arvizu RA</pubmed_authors><pubmed_authors>Lukas P</pubmed_authors><pubmed_authors>Kuszak AJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Vitamin D Standardization Program (VDSP) intralaboratory study for the assessment of 25-hydroxyvitamin D assay variability and bias.</name><description>An intralaboratory study assessing assay variability and bias for determination of serum total 25-hydroxyvitamin D [25(OH)D] was conducted by the Vitamin D Standardization Program (VDSP). Thirteen assays for serum total 25(OH)D were evaluated in a single laboratory including 11 unique immunoassays and one liquid chromatography - tandem mass spectrometry (LC-MS/MS) assay. Fifty single-donor serum samples, including eight samples with high concentrations of 25(OH)D&lt;sub>2&lt;/sub> (> 30 nmol/L), were assigned target values for 25(OH)D&lt;sub>2&lt;/sub> and 25(OH)D&lt;sub>3&lt;/sub> using reference measurement procedures (RMP). Using four replicate measurements for each sample, the mean total percent coefficient of variation (%CV) and mean % bias from the target values were determined for each assay using th</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2025-04-04T09:37:37.277Z</modification><creation>2025-04-04T09:37:37.277Z</creation></dates><accession>S-EPMC8403635</accession><cross_references><pubmed>34010687</pubmed><doi>10.1016/j.jsbmb.2021.105917</doi></cross_references></HashMap>