4.7 Article

Consistent Inverse Associations of Total, Bioavailable, Free, and Non-Bioavailable Vitamin D with Incidence of Diabetes among Older Adults with Lower Baseline HbA1c (≤6%) Levels

期刊

NUTRIENTS
卷 14, 期 16, 页码 -

出版社

MDPI
DOI: 10.3390/nu14163282

关键词

vitamin D; vitamin D-binding protein; bioavailable 25(OH)D; free 25(OH)D; type 2 diabetes

资金

  1. Saarland state Ministry for Social Affairs, Health, Women and Family Affairs (Saarbrucken, Germany)
  2. Baden-Wurttemberg state Ministry of Science, Research and Arts (Stuttgart, Germany)
  3. Federal Ministry of Education and Research (Berlin, Germany)
  4. Federal Ministry of Family Affairs, Senior Citizens, Women and Youth (Berlin, Germany)

向作者/读者索取更多资源

This large prospective cohort study in Germany found inverse associations between serum vitamin D-binding protein (VDBP), total bioavailable, complementary non-bioavailable, and free 25-hydroxyvitamin D (25(OH)D) levels and the risk of developing diabetes among non-diabetic older adults. However, associations were smaller and statistically insignificant for bioavailable and free 25(OH)D. The study also highlighted the importance of adequate vitamin D status among individuals without impaired glucose tolerance.
Background: Serum 25-hydroxyvitamin (25(OH)D) levels are inversely associated with risk of diabetes. The free hormone hypothesis suggests potential effects to be mainly related to concentrations of bioavailable and free rather than total 25(OH)D. We assessed associations of serum concentrations of vitamin D-binding protein (VDBP), as well as total bioavailable, complementary non-bioavailable, and free 25(OH)D, with the risk of developing diabetes among non-diabetic older adults in a large population-based cohort study in Germany. Methods: We included 4841 non-diabetic older adults aged 50-75 years at the baseline exam from the ESTHER cohort conducted in Saarland, Germany, in 2001-2002. Concentrations of bioavailable and free 25(OH)D were derived from serum concentrations of VDBP, total 25(OH)D, and albumin. Incidence of diabetes was ascertained during up to 14 years of follow-up. Associations were quantified by multivariable Cox proportional hazards regression models with comprehensive confounder adjustment. Results: During a median follow-up of 10.6 years, 837 non-diabetic participants developed diabetes. We observed similar inverse associations with developing diabetes for VDBP (hazard ratio (HR) for lowest versus highest quintile: 1.37, 95% confidence interval (CI): 1.09, 1.72), total 25(OH)D (HR: 1.31, 95% CI: 1.03, 1.66), and non-bioavailable 25(OH)D (HR: 1.30, 95% CI: 1.02, 1.65). Associations were smaller and statistically insignificant for bioavailable and free 25(OH)D. However, associations of total non-bioavailable, bioavailable, and free 25(OH)D with incidence of diabetes were much stronger among, and essentially restricted to, participants with lower baseline HbA(1c) (<= 6%) levels. Conclusions: This large prospective cohort study of older Caucasian adults, in agreement with results from randomized trials and Mendelian randomization studies, supports a protective effect of vitamin D against development of diabetes. The free hormone theory may not be relevant in this context. However, our results underline the importance of adequate vitamin D status among those who have not yet shown any sign of impaired glucose tolerance.

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