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Measurement by a Novel LC-MS/MS Methodology Reveals Similar Serum Concentrations of Vitamin D-Binding Protein in Blacks and Whites.

TitleMeasurement by a Novel LC-MS/MS Methodology Reveals Similar Serum Concentrations of Vitamin D-Binding Protein in Blacks and Whites.
Publication TypeJournal Article
Year of Publication2016
AuthorsHenderson CM, Lutsey PL, Misialek JR, Laha TJ, Selvin E, Eckfeldt JH
Secondary AuthorsHoofnagle AN
JournalClin Chem
Volume62
Issue1
Pagination179-87
Date Published2016 Jan
ISSN1530-8561
KeywordsAfrican 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.

DOI10.1373/clinchem.2015.244541
Alternate JournalClin Chem
PubMed ID26453697
PubMed Central IDPMC4698095
Grant ListHHSN268201100012C / 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