The Vitamin D Metabolite Ratio (VMR) is a Biomarker of Vitamin D Status That is Not Affected by Acute Changes in Vitamin D Binding Protein

被引:15
作者
Dugar, Anushree [1 ]
Hoofnagle, Andrew N. [2 ,3 ,4 ]
Sanchez, Amber P. [5 ]
Ward, David M. [5 ]
Corey-Bloom, Jody [6 ]
Cheng, Jonathan H. [5 ,7 ]
Ix, Joachim H. [5 ,7 ]
Ginsberg, Charles [5 ,8 ]
机构
[1] Univ Calif San Diego, Sch Med, San Diego, CA USA
[2] Univ Washington, Dept Lab Med, Seattle, WA USA
[3] Univ Washington, Dept Med, Seattle, WA USA
[4] Univ Washington, Kidney Res Inst, Seattle, WA USA
[5] Univ Calif San Diego, Div Nephrol Hypertens, San Diego, CA USA
[6] Univ Calif San Diego, Dept Neurosci, San Diego, CA USA
[7] Vet Affairs San Diego Healthcare Syst, Nephrol Sect, San Diego, CA USA
[8] Univ Calif San Diego, Div Nephrol Hypertens, 9452 Med Ctr Dr,L3E206, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
BONE-MINERAL DENSITY; 25-HYDROXYVITAMIN D; D DEFICIENCY; POPULATION; SERUM; OLDER; ASSOCIATION; FRACTURES; PLASMA; MEN;
D O I
10.1093/clinchem/hvad050
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background 25-hydroxyvitamin D[25(OH)D] may be a poor marker of vitamin D status due to variability in levels of vitamin D binding protein (VDBP). The vitamin D metabolite ratio (VMR) is the ratio of 24,25-dihydroxyvitamin D[24,25(OH)(2)D-3] to 25(OH)D-3 and has been postulated to reflect vitamin D sufficiency independent of variability in VDBP. Therapeutic plasma exchange (TPE) is a procedure that removes plasma, including VDBP, and may lower bound vitamin D metabolite concentrations. Effects of TPE on the VMR are unknown. Methods We measured 25(OH)D, free 25(OH)D, 1,25-dihydroxyvitamin D[1,25(OH)(2)D], 24,25(OH)(2)D-3, and VDBP in persons undergoing TPE, before and after treatment. We used paired t-tests to assess changes in these biomarkers during a TPE procedure. Results Study participants (n = 45) had a mean age of 55 +/- 16 years; 67% were female; and 76% were white. Compared to pretreatment concentrations, TPE caused a significant decrease in total VDBP by 65% (95%CI 60,70%), as well as all the vitamin D metabolites-25(OH)D by 66% (60%,74%), free 25(OH)D by 31% (24%,39%), 24,25(OH)(2)D-3 by 66% (55%,78%) and 1,25(OH)(2)D by 68% (60%,76%). In contrast, there was no significant change in the VMR before and after a single TPE treatment, with an observed mean 7% (-3%, 17%) change in VMR. Conclusions Changes in VDBP concentration across TPE parallel changes in 25(OH)D, 1,25(OH)(2)D, and 24,25(OH)(2)D-3, suggesting that concentrations of these metabolites reflect underlying VDBP concentrations. The VMR is stable across a TPE session despite a 65% reduction in VDBP. These findings suggest that the VMR is a marker of vitamin D status independent of VDBP levels.
引用
收藏
页码:718 / 723
页数:6
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