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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. | LitMetric

AI Article Synopsis

  • 25-hydroxyvitamin D (25(OH)D) levels can be misleading due to variations in vitamin D binding protein (VDBP), leading researchers to explore the vitamin D metabolite ratio (VMR) as a potentially more reliable indicator of vitamin D sufficiency.
  • A study involving 45 participants undergoing therapeutic plasma exchange (TPE) revealed significant decreases in VDBP and various vitamin D metabolites, while the VMR remained stable before and after treatment.
  • The findings indicate that the VMR can be a consistent marker for assessing vitamin D status, unaffected by changes in VDBP levels during TPE.

Article Abstract

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)2D3] to 25(OH)D3 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)2D], 24,25(OH)2D3, 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)2D3 by 66% (55%,78%) and 1,25(OH)2D 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)2D, and 24,25(OH)2D3, 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320009PMC
http://dx.doi.org/10.1093/clinchem/hvad050DOI Listing

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