Vitamin D3 supplementation improved exercise tolerance in deficient male COPD patients in small RCT
This 26-week, double-blind, randomized controlled trial enrolled 40 male smokers aged 40-80 years with stable COPD (post-bronchodilator FEV1/FVC <0.70) and vitamin D3 deficiency (serum 25(OH)D <30 ng/ml). The intervention group received oral vitamin D3 capsules: 80,000 IU/week for 13 weeks, followed by 40,000 IU per one to six weeks for another 13 weeks, adjusted according to serum 25(OH)D and calcium levels. The control group received placebo capsules. Both groups were advised daily sunlight exposure (5-15 minutes, 11am-4pm).
After 26 weeks, the vitamin D3 group showed statistically significant improvements compared to placebo in three secondary outcomes: 6-minute walk distance (p<0.05), dyspnea score (p<0.001), and fatigue score (p<0.001). The study did not report absolute numbers, effect sizes, or confidence intervals for these improvements. The primary outcome was not explicitly stated, and the study did not show improvement in ventilatory variables.
Safety and tolerability data were not reported. Key limitations include the small sample size (n=40), all-male population, and lack of reported effect sizes or absolute outcome numbers. All patients received sunlight exposure advice alongside the intervention or placebo, making it difficult to isolate the effect of supplementation alone. Funding sources and conflicts of interest were not reported.
For practice, this preliminary evidence suggests vitamin D3 supplementation may improve exercise tolerance and symptoms in vitamin D3-deficient male COPD patients, but the findings are limited by study size and design. Clinicians should interpret these results cautiously while awaiting larger, more comprehensive trials that include diverse patient populations and report complete outcome data.