Associations of Vitamin D-binding globulin and bioavailable Vitamin D concentrations with coronary heart disease events: The Multi-Ethnic Study of Atherosclerosis (MESA)

Cassianne Robinson-Cohen, Leila R. Zelnick, Andrew N. Hoofnagle, Pamela L. Lutsey, Gregory Burke, Erin D. Michos, Steven J.C. Shea, Russell Tracy, David S. Siscovick, Bruce Psaty, Bryan Kestenbaum, Ian H. De Boer

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Context: Low 25-hydroxyvitamin D [25(OH)D] is associated with coronary heart disease (CHD) in people who are white and Chinese but not black or Hispanic. Vitamin D binding globulin (VDBG) avidly binds 25(OH)D, reducing its bioavailability, and differs in isoform and concentration by race. Objective: Evaluate associations of VDBG with CHD and whether accounting for VDBG or estimating bioavailable 25(OH)D explains the heterogeneity of the association of 25(OH)D with CHD. Design and Setting: We conducted a case-cohort study within the Multi-Ethnic Study of Atherosclerosis. Participants with an incident CHD event over 12 years of follow-up (n = 538) and a randomly assigned subcohort (n = 999) were included. Wemeasured baseline 25(OH)D, VDBG, and isoforms using mass spectrometry and estimated bioavailable 25(OH)D from published equations. Results: VDBG was associated with an increased risk of CHD [hazard ratio, 1.77 (95% confidence interval, 1.46 to 2.14) per standard deviation increment, P < 0.0001], without evidence of heterogeneity by race or isoform (each P for interaction > 0.1). Low total 25(OH)D was differentially associated with CHD events, by race, with or without adjustment for VDBG (P for interaction = 0.04 or 0.05, respectively). Associations of 25(OH)D with CHD were strengthened with adjustment for VDBG among participants who were white or Chinese, and bioavailable 25(OH)D was associated with CHD events only among white participants. Conclusions: High VDBG concentration was associated with CHD events in all racial and ethnic groups. Incorporation of VDBG strengthened existing associations of 25(OH)D with CHD but did not explain racial heterogeneity in associations of 25(OH)D with CHD.

Original languageEnglish (US)
Pages (from-to)3075-3084
Number of pages10
JournalJournal of Clinical Endocrinology and Metabolism
Volume102
Issue number8
DOIs
StatePublished - Aug 1 2017

Bibliographical note

Funding Information:
This study was supported by National Heart, Lung, and Blood Institute Grant R01HL096875 and Grant N01-HC-95159 through N01-HC-95169. This study was also supported by National Institute of Diabetes and Digestive and Kidney Diseases Grant R01DK088762, Grant R01DK099199, and Grant K01DK109019.

Publisher Copyright:
© Copyright 2017 Endocrine Society.

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