Table 2

Sensitivity analyses

Change in P1NP, μg/LP valueChange in CTX, mg/LP value
Original study arms
 4000 IU/day (n=16)1.5 (−13.8 to 4.4)0.939.0 (−43.5 to 74.0)0.33
 2000 IU/day (n=12)−0.4 (−2.9 to 6.7)−8.5 (−45.5 to 8.0)
 Placebo (n=15)−1.1 (−6.8 to 13.0)−37.0 (−74.0 to 34.0)
Vitamin D repletion achieved
 Yes (n=13)1.5 (−0.5 to 5.3)0.40−3.0 (−48.0 to 10.0)0.74
 No (n=30)−1.2 (−8.3 to 8.4)−2.5 (−52.0 to 34.0)
Using glucocorticoids at baseline
 Vitamin D (n=12)−0.4 (−5.1 to 7.1)0.968.0 (−35.0 to 15.5)0.33
 Placebo (n=5)−1.2 (−6.8 to 3.8)−37.0 (−52.0 to −11.0)
Not using glucocorticoids at baseline
 Vitamin D (n=16)0.6 (−8.6 to 3.8)0.73−1.0 (−58.5 to 43.5)0.90
 Placebo (n=10)0.3 (−4.9 to 13.0)−10.0 (−74.0 to 46.0)
Interferon signature detectable at baseline
 Vitamin D (n=25)−0.5 (−8.3 to 2.2)0.521.0 (−48.0 to 14.0)0.22
 Placebo (n=11)−1.2 (−6.8 to 13.2)−40.0 (−84.0 to 34.0)
Interferon signature undetectable at baseline
 Vitamin D (n=3)15.8 (10.8 to 16.1)0.1631.0 (−39.0 to 364.0)0.87
 Placebo (n=4)0.3 (−5.0 to 7.4)22.0 (−27.0 to 493.5)
Subjects not using bisphosphonates at baseline
 Vitamin D (n=25)−0.2 (−4.0 to 4.1)0.636.0 (−39.0 to 17.0)0.51
 Placebo (n=14)0.3 (−4.9 to 13.0)−38.5 (−74.0 to 34.0)
  • P values from Kruskal-Wallis test for three-group comparison and Wilcoxon rank-sum test for two-group comparisons.