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. Author manuscript; available in PMC: 2014 Aug 1.
Published in final edited form as: Calcif Tissue Int. 2014 Feb;94(2):223–231. doi: 10.1007/s00223-013-9801-z

Table 5.

Women Within Each BMI Group Who Were on Treatment Before and After Fracture

Underweight (1) Non-obese (2) Obese (3) Significant P values
AOM use
 Before fracture 51.5 (39.6-63.3) 40.6 (38.7-42.5) 27.9 (24.7-31.2) (1) vs. (3)b, (2) vs. (3)b
 After fracture 63.2 (51.8-74.7) 46.3 (44.4-48.2) 33.2 (29.8-36.6) (1) vs. (3)b, (2) vs. (3)b, (1) vs. (2)a
Calcium & vitamin D
 Before fracture 34.9 (24.7-45.2) 39.9 (38.1-41.6) 38.6 (35.4-41.8)
 After fracture 45.8 (35.1-56.5) 45.2 (43.4-46.9) 45.5 (42.2-48.7)
AOM, calcium & vitamin D
 Before fracture 26.6 (15.7-37.4) 22.2 (20.6-23.8) 15.8 (13.1-18.4) (2) vs. (3)b
 After fracture 34.4 (22.7-46.0) 26.0 (24.3-27.7) 20.9 (17.9-23.9) (1) vs. (3)a, (2) vs. (3)a

Data are unadjusted percentages (95% confidence intervals)

AOM anti-osteoporosis medication, BMI body mass index

a

Alpha level ≤ 0.017 for pair-wise unadjusted comparisons

b

Alpha level ≤ 0.017 for pair-wise unadjusted and adjustedc comparisons

c

Adjusted for age, comorbidities (hypertension, heart disease, high cholesterol, asthma, emphysema, osteoarthritis and diabetes), and fracture type (clavicle, upper arm, wrist, spine, rib, hip, pelvis, ankle, upper and lower leg)