25-hydroxyvitamin-d-2 and Endocrine-System-Diseases

25-hydroxyvitamin-d-2 has been researched along with Endocrine-System-Diseases* in 1 studies

Reviews

1 review(s) available for 25-hydroxyvitamin-d-2 and Endocrine-System-Diseases

ArticleYear
Clinical review: The role of the parent compound vitamin D with respect to metabolism and function: Why clinical dose intervals can affect clinical outcomes.
    The Journal of clinical endocrinology and metabolism, 2013, Volume: 98, Issue:12

    There is no doubt that vitamin D must be activated to the hormonal form 1,25-dihydroxyvitamin D to achieve full biological activity or that many tissues participate in this activation process-be it endocrine or autocrine. We believe that not only is 25-hydroxyvitamin D important to tissue delivery for this activation process, but also that intact vitamin D has a pivotal role in this process.. In this review, evidence on the vitamin D endocrine/autocrine system is presented and discussed in relation to vitamin D-binding protein affinity, circulating half-lives, and enzymatic transformations of vitamin D metabolites, and how these affect biological action in any given tissue.. Circulating vitamin D, the parent compound, likely plays an important physiological role with respect to the vitamin D endocrine/autocrine system, as a substrate in many tissues, not originally thought to be important. Based on emerging data from the laboratory, clinical trials, and data on circulating 25-hydroxyvitamin D amassed during many decades, it is likely that for the optimal functioning of these systems, significant vitamin D should be available on a daily basis to ensure stable circulating concentrations, implying that variation in vitamin D dosing schedules could have profound effects on the outcomes of clinical trials because of the short circulating half-life of intact vitamin D.

    Topics: 25-Hydroxyvitamin D 2; Animals; Autocrine Communication; Calcifediol; Calcitriol; Dietary Supplements; Endocrine System; Endocrine System Diseases; Ergocalciferols; Humans; Vitamin D; Vitamin D Deficiency

2013