Standardizing Vitamin D Assays: The Way Forward

被引:165
作者
Binkley, Neil [1 ,2 ]
Sempos, Christopher T. [3 ]
机构
[1] Univ Wisconsin, Osteoporosis Clin Res Program, Madison, WI USA
[2] Univ Wisconsin, Inst Aging, Madison, WI USA
[3] NIH, Off Dietary Supplements, Bethesda, MD 20892 USA
关键词
VITAMIN D; STANDARDIZATION; VITAMIN D STANDARDIZATION PROGRAM; VDSP; 25-HYDROXYVITAMIN D; TANDEM MASS-SPECTROMETRY; 25-HYDROXYVITAMIN D; D METABOLITES; HUMAN SERUM; D-3; NUTRITION; PROGRAM;
D O I
10.1002/jbmr.2252
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
For a number of years it has been widely assumed that measurement of serum 25-hydroxyvitamin D [25(OH)D] concentration is the best approach to assessing an individual's vitamin D status.((1,2)) However, it has also been recognized that there is substantial within-assay variation in 25(OH)D measurement and even greater between-assay variability.((3-5)) Such assay variation clearly confounds attempts to define what constitutes the diagnosis of hypovitaminosis D. Importantly, assay variability makes pooling of 25(OH)D results from different studies in systematic reviews for the specific purpose of determining dose-response and/or clinical cut points at best problematic. Therefore, to develop and implement evidence-based clinical guidelines, it is essential that 25(OH)D measurement be standardized in both clinical and research laboratories. In this Perspective we outline a way forward toward achieving this goal-the Vitamin D Standardization Program (VDSP). (C) 2014 American Society for Bone and Mineral Research
引用
收藏
页码:1709 / 1714
页数:6
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