Abstract | AIMS/HYPOTHESIS: METHODS: At baseline, participants aged 35-56 years without known type 2 diabetes were examined using OGTTs, 25( OH)D and IGF peptide measurements, and anthropometric and lifestyle data. Participants who had prediabetes or type 2 diabetes at follow-up 8-10 years later were selected as cases; these were then age- and sex-matched to controls with normal glucose tolerance (NGT) at both baseline and follow-up, giving a total of 980 women and 1,398 men. RESULTS: Men but not women in the highest quartile of 25( OH)D level had a decreased OR for developing type 2 diabetes after adjustment for confounders (OR 0.52, 95% CI 0.30, 0.90), an effect accounted for by individuals with prediabetes, but not with NGT, at baseline. In both sexes, progression from prediabetes to type 2 diabetes was reduced by about 25% per 10 nmol/l increase in 25( OH)D. A high IGFBP-1 value was a better predictor of a reduced risk of type 2 diabetes than high 25( OH)D for both sexes, whereas high IGF-1 concentrations predicted a decreased risk only in men. CONCLUSIONS/INTERPRETATION: High serum 25( OH)D concentrations predict a reduced risk of type 2 diabetes in individuals with prediabetes, but not NGT. There were no significant interactions between 25( OH)D and IGFBP-1 or IGF-1 in terms of risk of diabetes. Our data suggest that vitamin D supplementation should be evaluated for the prevention of type 2 diabetes in prediabetic individuals.
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Authors | A Deleskog, A Hilding, K Brismar, A Hamsten, S Efendic, C-G Östenson |
Journal | Diabetologia
(Diabetologia)
Vol. 55
Issue 6
Pg. 1668-78
(Jun 2012)
ISSN: 1432-0428 [Electronic] Germany |
PMID | 22426800
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Somatomedins
- Vitamin D
- 25-hydroxyvitamin D
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Topics |
- Adult
- Diabetes Mellitus, Type 2
(blood, metabolism, pathology)
- Female
- Glucose Intolerance
(blood, metabolism, physiopathology)
- Glucose Tolerance Test
- Humans
- Male
- Middle Aged
- Prediabetic State
(blood, metabolism, physiopathology)
- Somatomedins
(metabolism)
- Vitamin D
(analogs & derivatives, blood)
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