TY - JOUR
T1 - Effect of vitamin D supplementation on glycaemic control and insulin resistance
T2 - a systematic review and meta-analysis
AU - George, P. S.
AU - Pearson, E. R.
AU - Witham, M. D.
N1 - Copyright 2012 Elsevier B.V., All rights reserved.
PY - 2012
Y1 - 2012
N2 - Aims To systematically review the evidence for the effect of vitaminD supplementation on glycaemia, insulin resistance, progression to diabetes and complications of diabetes. Methods Systematic review and meta-analysis. We searched databases including MEDLINE, EMBASE and the Cochrane Library for randomized controlled trials comparing vitaminD or analogues with placebo. We extracted data on fasting glucose, glycaemic control, insulin resistance, insulin/C-peptide levels, micro- and macrovascular outcomes and progression from non-diabetes to diabetes. Studies were assessed independently by two reviewers according to a pre-specified protocol. Results Fifteen trials were included in the systematic review. Trial reporting was of moderate, variable quality. Combining all studies, no significant improvement was seen in fasting glucose, HbA or insulin resistance in those treated with vitaminD compared with placebo. For patients with diabetes or impaired glucose tolerance, meta-analysis showed a small effect on fasting glucose (-0.32mmol/l, 95%CI -0.57 to -0.07) and a small improvement in insulin resistance (standard mean difference -0.25, 95%CI -0.48 to -0.03). No effect was seen on glycated haemoglobin in patients with diabetes and no differences were seen for any outcome in patients with normal fasting glucose. Insufficient data were available to draw conclusions regarding micro- or macrovascular events; two trials failed to show a reduction in new cases of diabetes in patients treated with vitaminD. Conclusions There is currently insufficient evidence of beneficial effect to recommend vitaminD supplementation as a means of improving glycaemia or insulin resistance in patients with diabetes, normal fasting glucose or impaired glucose tolerance.
AB - Aims To systematically review the evidence for the effect of vitaminD supplementation on glycaemia, insulin resistance, progression to diabetes and complications of diabetes. Methods Systematic review and meta-analysis. We searched databases including MEDLINE, EMBASE and the Cochrane Library for randomized controlled trials comparing vitaminD or analogues with placebo. We extracted data on fasting glucose, glycaemic control, insulin resistance, insulin/C-peptide levels, micro- and macrovascular outcomes and progression from non-diabetes to diabetes. Studies were assessed independently by two reviewers according to a pre-specified protocol. Results Fifteen trials were included in the systematic review. Trial reporting was of moderate, variable quality. Combining all studies, no significant improvement was seen in fasting glucose, HbA or insulin resistance in those treated with vitaminD compared with placebo. For patients with diabetes or impaired glucose tolerance, meta-analysis showed a small effect on fasting glucose (-0.32mmol/l, 95%CI -0.57 to -0.07) and a small improvement in insulin resistance (standard mean difference -0.25, 95%CI -0.48 to -0.03). No effect was seen on glycated haemoglobin in patients with diabetes and no differences were seen for any outcome in patients with normal fasting glucose. Insufficient data were available to draw conclusions regarding micro- or macrovascular events; two trials failed to show a reduction in new cases of diabetes in patients treated with vitaminD. Conclusions There is currently insufficient evidence of beneficial effect to recommend vitaminD supplementation as a means of improving glycaemia or insulin resistance in patients with diabetes, normal fasting glucose or impaired glucose tolerance.
UR - http://www.scopus.com/inward/record.url?scp=84863996265&partnerID=8YFLogxK
U2 - 10.1111/j.1464-5491.2012.03672.x
DO - 10.1111/j.1464-5491.2012.03672.x
M3 - Article
C2 - 22486204
AN - SCOPUS:84863996265
SN - 0742-3071
VL - 29
SP - e142-e150
JO - Diabetic Medicine
JF - Diabetic Medicine
IS - 8
ER -