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. 2011 Aug 31;94(4):1144–1149. doi: 10.3945/ajcn.111.015032

TABLE 2.

Effect of CaD supplements on health outcomes grouped by personal use of calcium and/or vitamin D supplements at randomization1

No personal calcium or vitamin D use2 Any personal calcium or vitamin D use2
CaD group(n = 7891) Placebo group(n = 7755) HR (95% CI) P3 CaD group(n = 10,285) Placebo group(n = 10,351) HR (95% CI) P3 P-interaction4
n (events/1000 patient-years) n (events/1000 patient-years) n (events/1000 patient-years) n (events/1000 patient-years)
Total cancer 633 (11.6) 715 (13.5) 0.86 (0.78, 0.96) 0.007 946 (13.7) 890 (12.8) 1.06 (0.97, 1.17) 0.20 0.003
Total breast cancer 261 (4.7) 310 (5.7) 0.82 (0.70, 0.97) 0.021 412 (5.9) 381 (5.4) 1.08 (0.94, 1.24) 0.27 0.012
Invasive breast cancer 209 (3.7) 256 (4.7) 0.80 (0.66, 0.96) 0.015 326 (4.6) 291 (4.1) 1.12 (0.96, 1.31) 0.16 0.005
In situ breast cancer 54 (1.0) 58 (1.1) 0.92 (0.63, 1.33) 0.65 89 (1.2) 91 (1.3) 0.98 (0.73, 1.31) 0.89 0.80
Colorectal cancer 67 (1.2) 82 (1.5) 0.83 (0.60, 1.15) 0.27 102 (1.4) 80 (1.1) 1.26 (0.94, 1.69) 0.12 0.044
Total fracture 892 (16.7) 892 (17.1) 0.98 (0.89, 1.07) 0.61 1210 (17.9) 1266 (18.7) 0.96 (0.89, 1.04) 0.32 0.72
Hip fracture 68 (1.2) 82 (1.5) 0.85 (0.61, 1.17) 0.31 107 (1.5) 117 (1.6) 0.93 (0.71, 1.21) 0.59 0.65
All-cause mortality 336 (5.9) 349 (6.3) 0.94 (0.81, 1.10) 0.44 408 (5.7) 458 (6.4) 0.88 (0.77, 1.01) 0.06 0.44
1

CaD, calcium and vitamin D.

2

Personal calcium or vitamin D refers to use of nonprotocol calcium and/or vitamin D supplements at randomization.

3

P values obtained from Cox proportional hazards models stratified by age, randomization status in the Women's Health Initiative hormone and dietary modification trials, and relevant prevalent disease at baseline (history of breast cancer, colorectal cancer, or any cancer for breast, colorectal, and total cancer endpoints and history of fracture for hip and total fracture).

4

Interaction between CaD allocation and use or nonuse of personal calcium and/or vitamin D supplements at randomization for each endpoint tested in Cox proportional hazard models.