Vitamin D Supplementation and Cognition in People with Type 2 Diabetes: A Randomized Control Trial

الملخص EN

Aim.

Type 2 diabetes increases the risk of cognitive decline which adversely impacts self-management of the disease.

Evidence also supports a relationship between low serum 25(OH)D levels and poor cognition.

The purpose of this trial was to assess vitamin D supplementation on cognitive executive functioning in persons living with type 2 diabetes.

Methods.

This was a double-blinded RCT where participants were randomized to receive either weekly vitamin D3 supplementation (50,000 IUs) or a matching comparator (5,000 IUs) for three months.

The primary outcome was a battery of neuropsychological tests.

Serum 25(OH)D was measured by liquid chromatography/tandem mass spectrometry.

Repeated assessments of cognitive measures were collected over 12 weeks using alternative testing forms to minimize practice effects.

Results.

Thirty participants were randomized to either the low-dose allocation (n=15) or the high-dose allocation (n=15).

Most participants were female (83%) and identified as Black (57%).

For all cognition measures, there was no statistically significant finding between participants who received high-dose vitamin D supplementation and those who received low-dose supplementation.

However, when assessing cognitive function in both groups over time, minimal improvement on the Symbol-Digits, the Stroop Interference Test, and the Trail Making Test Part B was observed.

Conclusions.

To our knowledge, this is the first randomized control trial to examine the effects of vitamin D supplementation on cognitive function in people with type 2 diabetes.

However, no significant differences in cognitive outcomes between participants who received high-dose therapy and those who received low dose were found.