Race, Ancestry, and Vitamin D Metabolism: The Multi-Ethnic Study of Atherosclerosis

Author:

Hsu Simon1ORCID,Hoofnagle Andrew N2,Gupta Deepak K34,Gutierrez Orlando M56,Peralta Carmen A789,Shea Steven1011,Allen Norrina B12,Burke Gregory13,Michos Erin D1415,Ix Joachim H1617,Siscovick David18,Psaty Bruce M1920,Watson Karol E21,Kestenbaum Bryan1,de Boer Ian H1,Robinson-Cohen Cassianne2223ORCID

Affiliation:

1. Kidney Research Institute, Division of Nephrology, Department of Medicine, University of Washington, Seattle, Washington

2. Department of Laboratory Medicine, University of Washington, Seattle, Washington

3. Vanderbilt Translational and Clinical Cardiovascular Research Center, Vanderbilt University Medical Center, Nashville, Tennessee

4. Division of Cardiovascular Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee

5. Division of Nephrology, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama

6. Department of Epidemiology, University of Alabama at Birmingham, Birmingham, Alabama

7. Cricket Health, Inc., San Francisco, California

8. The Kidney Health Research Collaborative, San Francisco, California

9. University of California, San Francisco, San Francisco, California

10. Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York

11. Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York

12. Department of Internal Medicine, Northwestern University, Chicago, Illinois

13. Division of Public Health Sciences Wake Forest School of Medicine, Winston-Salem, North Carolina

14. Division of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland

15. Department of Epidemiology and the Welch Center for Prevention, Epidemiology and Clinical Research, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland

16. Nephrology Section, Veterans Affairs San Diego Healthcare System, San Diego, California

17. Division of Nephrology-Hypertension, University of California, San Diego, San Diego, California

18. New York Academy of Medicine, New York, New York

19. Cardiovascular Health Research Unit, Departments of Medicine, Epidemiology and Health Services, University of Washington, Seattle, Washington

20. Kaiser Permanente Washington Health Research Institute, Seattle, Washington

21. Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California

22. Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee

23. Vanderbilt Center for Kidney Disease, Vanderbilt University Medical Center, Nashville, Tennessee

Abstract

Abstract Context A comprehensive characterization of racial/ethnic variations in vitamin D metabolism markers may improve our understanding of differences in bone and mineral homeostasis and the risk of vitamin D–related diseases. Objective Describe racial/ethnic differences in vitamin D metabolism markers and their associations with genetic ancestry. Design, Setting, Participants In a cross-sectional study within the Multi-Ethnic Study of Atherosclerosis (MESA), we compared a comprehensive panel of vitamin D metabolism markers across self-reported racial/ethnic groups of Black (N = 1759), White (N = 2507), Chinese (N = 788), and Hispanic (N = 1411). We evaluated associations of proportion African and European ancestry with this panel of markers in Black and Hispanic participants using ancestry informative markers. Latent class analysis evaluated associations between patterns of vitamin D measurements with race/ethnicity. Results Compared with Black participants, White participants had significantly higher serum concentrations of 25-hydroxyvitamin D and fibroblast growth factor-23; lower concentrations of parathyroid hormone and 1,25-dihydroxyvitamin D; circulating vitamin D metabolite ratios suggesting lower CYP27B1 and higher CYP24A1 activity; higher urinary concentrations of calcium and phosphorus with higher urinary fractional excretion of phosphorus; and differences in vitamin D binding globulin haplotypes. Higher percent European ancestry was associated with higher 25-hydroxyvitamin D and lower parathyroid hormone concentrations among Black and Hispanic participants. Latent classes defined by vitamin D measurements reflected these patterns and differed significantly by race/ethnicity and ancestry. Conclusions Markers of vitamin D metabolism vary significantly by race/ethnicity, may serve to maintain bone and mineral homeostasis across ranges of 25-hydroxyvitamin D production, and be attributable, at least partly, to genetic ancestry.

Funder

National Heart, Lung, and Blood Institute

National Center for Advancing Translational Sciences

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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