Title | Measurement by a Novel LC-MS/MS Methodology Reveals Similar Serum Concentrations of Vitamin D-Binding Protein in Blacks and Whites. |
Publication Type | Journal Article |
Year of Publication | 2016 |
Authors | Henderson CM, Lutsey PL, Misialek JR, Laha TJ, Selvin E, Eckfeldt JH |
Secondary Authors | Hoofnagle AN |
Journal | Clin Chem |
Volume | 62 |
Issue | 1 |
Pagination | 179-87 |
Date Published | 2016 Jan |
ISSN | 1530-8561 |
Keywords | African Continental Ancestry Group, Chromatography, Liquid, European Continental Ancestry Group, Female, Genotype, Humans, Immunoassay, Male, Tandem Mass Spectrometry, United States, Vitamin D-Binding Protein |
Abstract | BACKGROUND: Vitamin D deficiency is associated with poor bone health and other adverse health outcomes; however, the associations are greatly attenuated in black vs white individuals. One possible explanation for this attenuation is different concentrations of bioavailable vitamin D metabolites in plasma, which are estimated with equations that include the total concentration of vitamin D binding globulin (VDBG) and haplotype-specific dissociation constants. METHODS: We developed a method to quantify VDBG with LC-MS/MS that could also identify the haplotypes/isoforms of VDBG present. We validated the method according to recent recommendations for publications of biomarker studies. We determined serum VDBG concentrations in samples from the Atherosclerosis Risk in Communities cohort and compared the results with a widely used monoclonal immunoassay. RESULTS: With 10 μL of serum or plasma, the lower limit of quantification for the assay ( CONCLUSIONS: Validated mass spectrometric methods for the quantification of proteins in human samples can provide additional information beyond immunoassay. Counter to prior observations by immunoassay, VDBG concentrations did not vary by race. |
DOI | 10.1373/clinchem.2015.244541 |
Alternate Journal | Clin Chem |
PubMed ID | 26453697 |
PubMed Central ID | PMC4698095 |
Grant List | HHSN268201100012C / HL / NHLBI NIH HHS / United States T32 HL007028 / HL / NHLBI NIH HHS / United States U24 CA160034 / CA / NCI NIH HHS / United States HHSN268201100009I / HL / NHLBI NIH HHS / United States R01 HL103706 / HL / NHLBI NIH HHS / United States HHSN268201100010C / HL / NHLBI NIH HHS / United States HHSN268201100008C / HL / NHLBI NIH HHS / United States HHSN268201100005G / HL / NHLBI NIH HHS / United States HHSN268201100008I / HL / NHLBI NIH HHS / United States HHSN268201100005C / / PHS HHS / United States R01 DK089174 / DK / NIDDK NIH HHS / United States HHSN268201100007C / HL / NHLBI NIH HHS / United States HHSN268201100009C / / PHS HHS / United States HHSN268201100011I / HL / NHLBI NIH HHS / United States HHSN268201100011C / HL / NHLBI NIH HHS / United States HHSN268201100010C / / PHS HHS / United States HHSN268201100006C / HL / NHLBI NIH HHS / United States HHSN268201100008C / / PHS HHS / United States HHSN268201100012C / / PHS HHS / United States HHSN268201100005I / HL / NHLBI NIH HHS / United States K24 DK106414 / DK / NIDDK NIH HHS / United States CA160034 / CA / NCI NIH HHS / United States HL007028 / HL / NHLBI NIH HHS / United States HHSN268201100007C / / PHS HHS / United States DK089174 / DK / NIDDK NIH HHS / United States P30 DK035816 / DK / NIDDK NIH HHS / United States HHSN268201100009C / HL / NHLBI NIH HHS / United States HHSN268201100011C / / PHS HHS / United States HHSN268201100005C / HL / NHLBI NIH HHS / United States HL103706 / HL / NHLBI NIH HHS / United States HHSN268201100007I / HL / NHLBI NIH HHS / United States DK035816 / DK / NIDDK NIH HHS / United States HHSN268201100006C / / PHS HHS / United States HL103706-S1 / HL / NHLBI NIH HHS / United States |