| Literature DB >> 33266123 |
Cherlyn Ding1, Zhiling Chan1, Yu Chung Chooi1, John Choo1, Suresh Anand Sadananthan1, Navin Michael1, Sambasivam Sendhil Velan1,2,3,4, Melvin Khee-Shing Leow1,4,5,6,7, Faidon Magkos8.
Abstract
The association between low vitamin D status and the development of type 2 diabetes mellitus is well established; however, intervention trials that increased serum vitamin D (through ultraviolet B exposure or dietary supplementation) provide mixed outcomes. Recent evidence suggests that metabolites directly related to vitamin D receptor activation-1α,25-dihydroxyvitamin D3 and 24R,25-dihydroxyvitamin D3-may be better markers of vitamin D repletion status. We tested the hypothesis that a vitamin D metabolite (VDM) index, calculated as the sum of normalized fasting serum concentrations of 1α,25-dihydroxyvitamin D3 and 24R,25-dihydroxyvitamin D3, is associated with metabolic function. We measured subcutaneous and visceral adipose tissue volume, intrahepatic triglyceride content, maximum oxygen uptake, insulin sensitivity (4 h hyperinsulinemic-euglycemic clamp), and insulin secretion (3 h meal tolerance test with mathematical modeling) and calculated the VDM index in 65 healthy Asian adults. Subjects with a low VDM index had lower peripheral insulin sensitivity and beta-cell function compared to subjects with a high VDM index (both p < 0.05), matched for age, sex, BMI, and serum 25-hydroxyvitamin D3. Serum 25-hydroxyvitamin D3 was not associated with peripheral insulin sensitivity or beta-cell function. Our results suggest that, rather than enhancing vitamin D substrate availability, upregulation of vitamin D action is more likely to lead to improvements in glucose homeostasis.Entities:
Keywords: glucose homeostasis; metabolic dysfunction; vitamin D metabolites
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Year: 2020 PMID: 33266123 PMCID: PMC7760638 DOI: 10.3390/nu12123706
Source DB: PubMed Journal: Nutrients ISSN: 2072-6643 Impact factor: 5.717