25(OH)D2 Half-Life Is Shorter Than 25(OH)D3 Half-Life and Is Influenced by DBP Concentration and Genotype

被引:196
作者
Jones, K. S. [1 ,2 ]
Assar, S. [1 ]
Harnpanich, D. [1 ]
Bouillon, R. [3 ]
Lambrechts, D. [4 ,5 ]
Prentice, A. [1 ,2 ]
Schoenmakers, I. [1 ]
机构
[1] Med Res Council Human Nutr Res, Cambridge CB1 9NL, England
[2] Med Res Council Keneba, Keneba, Gambia
[3] Katholieke Univ Leuven, Clin & Lab Expt Med & Endocrinol, B-3000 Leuven, Belgium
[4] Katholieke Univ Leuven, Lab Translat Genet, B-3000 Leuven, Belgium
[5] Katholieke Univ Leuven, Vesalius Res Ctr, VIB, B-3000 Leuven, Belgium
基金
英国医学研究理事会;
关键词
D-BINDING PROTEIN; VITAMIN-D DEFICIENCY; SERUM 25-HYDROXYVITAMIN D; PLASMA-CONCENTRATIONS; D-2; CHOLECALCIFEROL; ERGOCALCIFEROL; MECHANISM; WOMEN; SUPPLEMENTATION;
D O I
10.1210/jc.2014-1714
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: There is uncertainty over the equivalence of vitamins D-2 and D-3 to maintain plasma 25-hydroxyvitamin D (25(OH)D). Objective: The objective of the study was to compare the plasma half-lives of 25(OH)D-2 and 25(OH)D-3 in two distinct populations with different dietary calcium intake and 25(OH)D status. Participants: Healthy men (aged 24 and 39 y), resident in The Gambia (n = 18) or the United Kingdom (n = 18) participated in the study. Interventions: The intervention included an oral tracer dose of deuterated-25(OH)D-2 and deuterated-25(OH)D-3 (both 40 nmol). Blood samples were collected over 33 days. Main Outcome Measures: 25(OH)D-2 and 25(OH)D-3 plasma half-lives, concentrations of 25(OH)D, and vitamin D binding protein (DBP) and DBP genotypes were measured. Results: 25(OH)D-2 half-life [mean (SD)] [13.9 (2.6) d] was shorter than 25(OH)D-3 half-life [15.1 (3.1) d; P = .001] for countries combined, and in Gambians [12.8 (2.3) d vs 14.7 (3.5) d; P < .001], but not in the United Kingdom [15.1 (2.4) d vs 15.6 (2.5) d; P = .3]. 25(OH)D concentration was 69 (13) and 29 (11) nmol/L (P < .0001), and the DBP concentration was 259 (33) and 269 (23) mg/L (P = .4) in The Gambia and United Kingdom, respectively. Half-lives were positively associated with plasma DBP concentration for countries combined [25(OH)D-2 half-life: regression coefficient (SE) 0.03 (0.01) d per 1 mg/L DBP, P = .03; 25(OH)D-3 half-life: 0.04 (0.02) d, P = .02] and in Gambians[25(OH)D-2 half-life: 0.04 (0.01) d; P = .02; 25(OH)D-3 half-life: 0.06 (0.02) d, P = .01] but not in UK participants. The DBP concentration x country interactions were not significant. DBP Gc1f/1f homozygotes had shorter 25(OH)D-2 half-lives compared with other combined genotypes (P = .007) after correction for country. Conclusions: 25(OH)D-2 half-life was shorter than 25(OH)D-3 half-life, and half-lives were affected by DBP concentration and genotype. The stable isotope 25(OH)D half-life measurements provide a novel tool to investigate vitamin D metabolism and vitamin D expenditure and aid in the assessment of vitamin D requirements.
引用
收藏
页码:3373 / 3381
页数:9
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