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. Author manuscript; available in PMC: 2014 Feb 7.
Published in final edited form as: Scand J Infect Dis. 2011 Oct 25;44(2):126–132. doi: 10.3109/00365548.2011.621446

Table II.

Details of intervention studies included.

Location Subjects Main outcome measure Intervention
Tromsø 1, Norway Subjects with reduced glucose tolerance Development of type 2 diabetes 20,000 IU vitamin D3 per week or placebo
Tromsø 2, Norway Subjects with serum 25(OH)D < 50 nmol/l Blood pressure, lipids, depression 40,000 IU vitamin D3 per week or placebo
Tromsø 3, Norway Subjects with serum 25(OH)D < 50 nmol/l Glucose sensitivity 40,000 IU vitamin D3 per week or placebo
Vienna, Austria Kidney transplant recipients with 25(OH)D < 50 nmol/l Graft function 6800 IU vitamin D3 per day or placebo
Seattle, USA Type 2 diabetes with 25(OH) D < 75 nmol/l and urine albumin excretion ≥ 30 mg/day Urine albumin excretion 2000 IU vitamin D3 per day or placebo
Dundee 1, Scotland Age > 70 y, isolated systolic hypertension and 25(OH)D < 75 nmol/l Blood pressure 100,000 units vitamin D3 or placebo, taken at 0, 3, 6, and 9 months
Dundee 2, Scotland Adults with a past history of myocardial infarction Change in endothelial function 100,000 units vitamin D3 or placebo, taken at 0, 2, and 4 months
Dundee 3, Scotland Adults with resistant hypertension and 25(OH)D level < 75 nmol/l Blood pressure 100,000 units vitamin D3 or placebo, taken at 0, 2, and 4 months
Aarhus, Denmark Subjects with serum 25(OH) D < 80 nmol/l PTH and calcium metabolism 2800 IU vitamin D3 per day or placebo
Leuven, Belgium Patients with moderate to very severe COPD COPD exacerbations 100,000 units vitamin D3 or placebo every 4 weeks during 1 y

25(OH)D, 25-hydroxyvitamin D; PTH, parathyroid hormone; COPD, chronic obstructive pulmonary disease.