Hundred and fourteen DMD boys, average age 15.1 years (range 4-25 years), 69.3% (n=79) deletion/duplications, 24.5% (n=28) point mutations, 6.1% (n=7) unrecorded genetics were included. 65% (n=74) received steroids, 63% (n=72) were non-ambulatory. Three hundred and two 25OHD values were available with an average of 26.12 ng/ml (range <13-83 ng/ml). Sub-group analysis showed statistically significant difference (p<0.05) with higher vitD levels in ambulatory boys age <12 years, with no difference in steroid versus steroid naive group. Prospectively, 52 subjects with vitD deficiency enrolled in BHP with 15 subjects completing 6 months follow-up, showing statistically significant improvement in 25OHD levels.