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The Vitamin D Metabolite Ratio Is Independent of Vitamin D Binding Protein Concentration.
Ginsberg, Charles; Hoofnagle, Andrew N; Katz, Ronit; Becker, Jessica O; Kritchevsky, Stephen B; Shlipak, Michael G; Sarnak, Mark J; Ix, Joachim H.
  • Ginsberg C; Division of Nephrology-Hypertension, University of California, San Diego, San Diego, CA.
  • Hoofnagle AN; Department of Laboratory Medicine and the Kidney Research Institute, University of Washington, Seattle, WA.
  • Katz R; Department of Medicine and the Kidney Research Institute, University of Washington, Seattle, WA.
  • Becker JO; Kidney Research Institute, University of Washington, Seattle, WA.
  • Kritchevsky SB; Department of Laboratory Medicine and the Kidney Research Institute, University of Washington, Seattle, WA.
  • Shlipak MG; Department of Medicine and the Kidney Research Institute, University of Washington, Seattle, WA.
  • Sarnak MJ; Department of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, NC.
  • Ix JH; Kidney Health Research Collaborative, Veterans Affairs Medical Center, San Francisco, CA.
Clin Chem ; 67(2): 385-393, 2021 01 30.
Article en En | MEDLINE | ID: mdl-33188595
BACKGROUND: 25-Hydroxyvitamin D [25(OH)D] may be a poor marker of vitamin D status as it reflects differences in vitamin D binding protein (VDBP) between individuals. The vitamin D metabolite ratio [VMR, ratio of 24,25(OH)2D3 to 25(OH)D3] is a marker of vitamin D status that has been hypothesized to be independent of variability in VDBP. This hypothesis has not been directly evaluated. METHODS: We measured 25(OH)D3, 24,25(OH)2D3, 1,25(OH)2D3, and VDBP in 377 community-dwelling older adults that participated in the Health Aging and Body Composition Study. 24,25(OH)2D3 and 25(OH)D3 were used to calculate the VMR. We used linear regression to assess the relationship between VDBP with the VMR, 24,25(OH)2D3, 25(OH)D3, and 1,25(OH)2D3. RESULTS: Participants had mean age 75 ± 3 years, 52% were female, 40% were black, and 24% had chronic kidney disease. VDBP concentrations were associated with sex, serum albumin, and VDBP phenotype in multivariable models. In fully adjusted models, each 1% higher VDBP was associated with a 0.92%[95% CI(0.37,1.49%)], 0.76% (0.39, 1.13%), and 0.57% (0.29, 0.85%), higher 24,25(OH)2D3, 25(OH)D3, and 1,25(OH)2D3. The VMR was independent of VDBP concentration, [0.16%(-0.11, 0.44) higher VMR per 1% higher VDBP, P = .25]. CONCLUSIONS: The VMR was independent of VDBP concentration, whereas VDBP was strongly directly associated with the individual vitamin D metabolite concentrations. Prior studies evaluating only 25(OH)D3 may have been confounded by absence of data on VDBP status. The VMR may serve as an important biomarker of vitamin D status and clinical outcomes that can be utilized in populations with a large spectrum of VDBP concentrations.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vitamina D / Proteína de Unión a Vitamina D / Deficiencia de Vitamina D Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vitamina D / Proteína de Unión a Vitamina D / Deficiencia de Vitamina D Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male Idioma: En Año: 2021 Tipo del documento: Article