Serum 25-hydroxyvitamin D in the VITamin D and OmegA-3 TriaL (VITAL): Clinical and demographic characteristics associated with baseline and change with randomized vitamin D treatment

Heike Luttmann-Gibson, Samia Mora, Carlos A Camargo, Nancy R Cook, Olga V Demler, Amit Ghoshal, Jay Wohlgemuth, Kris Kulkarni, Julia Larsen, James Prentice, Michael Cobble, Vadim Bubes, Chunying Li, Georgina Friedenberg, I-Min Lee, Julie E Buring, JoAnn E Manson, Heike Luttmann-Gibson, Samia Mora, Carlos A Camargo, Nancy R Cook, Olga V Demler, Amit Ghoshal, Jay Wohlgemuth, Kris Kulkarni, Julia Larsen, James Prentice, Michael Cobble, Vadim Bubes, Chunying Li, Georgina Friedenberg, I-Min Lee, Julie E Buring, JoAnn E Manson

Abstract

Background: The VITamin D and OmegA-3 TriaL (VITAL) is a completed randomized, placebo-controlled trial of vitamin D3 (2000 IU/day) and marine omega-3 (1 g/day) supplements in the primary prevention of cancer and cardiovascular disease. Here we examine baseline and change in 25-hydroxyvitamin D (25(OH)D) and related biomarkers with randomized treatment and by clinical factors.

Methods: Baseline 25(OH)D was measured in 15,804 participants (mean age 68 years.; 50.8% women; 15.7% African Americans) and in 1660 1-year follow-up samples using liquid chromatography-tandem mass spectrometry and chemiluminescence. Calcium and parathyroid hormone (iPTH) were measured by chemiluminescence and spectrophotometry respectively.

Results: Mean baseline total 25(OH)D (ng/mL ± SD) was 30.8 ± 10.0 ng/mL, and correlated inversely with iPTH (r = -0.28), p < .001. After adjusting for clinical factors, 25(OH)D (ng/mL ± SE) was lower in men vs women (29.7 ± 0.30 vs 31.4 ± 0.30, p < .0001) and in African Americans vs whites (27.9 ± 0.29 vs 32.5 ± 0.22, p < .0001). It was also lower with increasing BMI, smoking, and latitude, and varied by season. Mean 1-year 25(OH)D increased by 11.9 ng/mL in the active group and decreased by 0.7 ng/mL in placebo. The largest increases were noted among individuals with low baseline and African Americans. Results were similar for chemiluminescent immunoassay. Mean calcium was unchanged, and iPTH decreased with treatment.

Conclusion: In VITAL, baseline 25(OH)D varied by clinical subgroups, was lower in men and African Americans. Concentrations increased with vitamin D supplementation, with the greatest increases in those with lower baseline 25(OH)D. The seasonal trends in 25(OH)D, iPTH, and calcium may be relevant when interpreting 25(OH)D levels for clinical treatment decisions.

Clinical trial registration: VITAL ClinicalTrials.gov number NCT01169259.

Keywords: 25-hydroxyvitamin D; Parathyroid hormone; Seasonal effects; VITAL trial; Vitamin D.

Copyright © 2019 Elsevier Inc. All rights reserved.

Figures

Figure 1:
Figure 1:
Spearman correlation coefficients between 25(OH)D total and 25(OH)D3 measured by LC-MS/MS (ng/mL), 25(OH)D total measured by chemiluminescent microparticle immunoassay (CMIA) (ng/mL), Calcium (mg/dL) and iPTH (pg/ml). Based on 15804 measurements at baseline.
Figure 2:
Figure 2:
Seasonal trend of weekly baseline (pre-randomization) total 25(OH)D (LC-MS/MS), Calcium and iPTH averages over the course of the study. Fitted curve was modeled as a linear function of sine and cosine terms with period of one year, adjusted for age, gender, race, BMI, smoking status, and latitude. Based on a total of 7502 (25(OH)D), 7447 (Ca), and 7474 (iPTH) baseline measurements from subjects without non-randomized vitamin D or calcium supplements; red dots: weekly means based on 3 or less measurements.
Figure 3:
Figure 3:
Mean baseline 25(O)D (+95% confidence intervals) associated with subject characteristic. Multivariable linear regression model of total 25(OH)D levels and all listed covariates, additionally adjusted for age, BMI, latitude, and season. Ca= non-randomized calcium supplements, VitD=non-randomized VitD supplement, Diab=Diabetes, Hyper=Hypertension, NStat=non-statin lipid-lowering

Source: PubMed

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