Table 1

Baseline clinical characteristics of the recruited patients

Mean (SD)/number (%)
Raloxifene (N=57)Placebo (N=57)p Value
Age, years55.4 (7.8)55.2 (7.6)0.93
Duration of menopause, years8.6 (8.3)8.3 (7.2)0.81
Parity2.1 (1.2)2.2 (1.4)0.60
Duration of GC treatment, months58.1 (63.5)67.8 (58.7)0.40
Daily dose of prednisolone, mg7.2 (6.2)6.5 (5.5)0.52
Daily prednisolone dose ≥7.5 mg21 (37)16 (28)0.32
Body mass index, kg/m223.2 (3.5)24.1 (3.6)0.18
Ever smoking2 (4)5 (9)0.44
Underlying diseases
 SLE30 (53)32 (56)0.71
 RA16 (28)15 (26)0.83
 Inflammatory myopathy4 (7)1 (2)0.36
 Others7 (12)9 (16)0.59
Cumulative prednisolone dose in the 12-month study period, g2.17 (1.20)1.97 (0.76)0.28
Bone mineral density, g/cm2
 Lumbar spine0.864 (0.136)0.848 (0.147)0.55
Total hip0.741 (0.136)0.780 (0.146)0.16
 Femoral neck0.647 (0.117)0.683 (0.126)0.13
 Whole body1.013 (0.123)0.993 (0.113)0.37
Naive to calcium18 (32)15 (26)0.54
Naive to calcitriol43 (75)42 (74)0.83
Naive to antiosteoporotic medications51 (89)54 (95)0.30
Vertebral fracture4 (7)2 (4)0.68
Total cholesterol, mmol/litre5.28 (1.08)5.36 (1.18)0.73
LDL cholesterol, mmol/litre2.84 (0.92)2.91 (1.08)0.70
HDL cholesterol, mmol/litre1.77 (0.61)1.79 (0.53)0.85
Triglyceride, mmol/litre1.45 (0.67)1.43 (0.71)0.88
  • GC, glucocorticoid; HDL, high-density lipoprotein; LDL, low-density lipoprotein; RA, rheumatoid arthritis; SLE, systemic lupus erythematosus.