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1 oteins increase the risk of osteoporosis and osteoporotic fracture.
2 Vertebral fractures are the most common osteoporotic fracture.
3 d bone mineral density and increased risk of osteoporotic fracture.
4 to maximize efficacy in patients at risk for osteoporotic fracture.
5 ross-linking, thereby increasing the risk of osteoporotic fracture.
6 ed to low bone density and increased risk of osteoporotic fracture.
7 , bone mineral density, and the incidence of osteoporotic fracture.
8 functioning and thus may reduce the risk for osteoporotic fracture.
9 ement bone densitometry in assessing risk of osteoporotic fracture.
10 at is significantly related to bone mass and osteoporotic fracture.
11 ccurately identify those at greatest risk of osteoporotic fracture.
12 The primary endpoint was time to first osteoporotic fracture.
13 rs) after cohort entry for an incident major osteoporotic fracture.
14 ral density (BMD) predicts the likelihood of osteoporotic fracture.
15 lomipramine (CLP), have an increased risk of osteoporotic fracture.
16 up, 21 (4.6%) recipients experienced a major osteoporotic fracture.
17 ure and 113 participants experienced a major osteoporotic fracture.
18 fully improve the prediction of hip or major osteoporotic fracture.
19 a means to improve bone strength and reduce osteoporotic fracture.
20 tate cancer is associated with bone loss and osteoporotic fractures.
21 ars of age who were enrolled in the Study of Osteoporotic Fractures.
22 independent risk factor for osteoporosis and osteoporotic fractures.
23 Patients with RA are at increased risk of osteoporotic fractures.
24 gnificant gene BDNF was also associated with osteoporotic fractures.
25 or =65 years of age enrolled in the Study of Osteoporotic Fractures.
26 of the hip in elderly women in the Study of Osteoporotic Fractures.
27 at the baseline examination of the Study of Osteoporotic Fractures.
28 at the baseline examination of the Study of Osteoporotic Fractures.
29 hosphonates are a common treatment to reduce osteoporotic fractures.
30 rly women are associated with a reduction in osteoporotic fractures.
31 uman beings and thereby decrease the risk of osteoporotic fractures.
32 c kidney disease, chronic liver disease, and osteoporotic fractures.
33 es may be consistent with a reduction in all osteoporotic fractures.
34 at 26 million American women are at risk for osteoporotic fractures.
35 od most often used to determine the risk for osteoporotic fractures.
36 of sex and racial differences in the risk of osteoporotic fractures.
37 of age or older and enrolled in the Study of Osteoporotic Fractures.
38 Ps in the setting of secondary prevention of osteoporotic fractures.
39 ysteine concentrations are a risk factor for osteoporotic fractures.
40 but also to contribute to the development of osteoporotic fractures.
41 frican-American participants in the Study of Osteoporotic Fractures.
42 associated with a 4-fold increased risk for osteoporotic fractures.
43 hniques should be used to diagnose prevalent osteoporotic fractures.
44 om bisphosphonate-treated women with typical osteoporotic fractures.
45 1 older US women from the Caregiver-Study of Osteoporotic Fractures.
46 and April 2004 in a substudy of the Study of Osteoporotic Fractures.
47 eric femur that are infrequently affected by osteoporotic fractures.
48 d the exercise type most effective to reduce osteoporotic fractures.
49 t been systematically studied in relation to osteoporotic fractures.
50 tive was to examine FA intake in relation to osteoporotic fractures.
51 wered hip BMD but did not change the risk of osteoporotic fractures.
52 , and low risk of fractures [HR (95% CI) for osteoporotic fractures: 0.90 (0.83, 0.96); for hip fract
53 and high risk of fractures [HR (95% CI) for osteoporotic fractures: 1.08 (1.00, 1.06); for hip fract
55 52 patients were reviewed (121 patients with osteoporotic fractures, 30 with malignant disease, and o
57 ls, among 6,653 participants in the Study of Osteoporotic Fractures, a community-based, prospective c
58 linical centers and enrolled in the Study of Osteoporotic Fractures, a longitudinal cohort study.
60 did not have a significantly reduced risk of osteoporotic fracture, although there was a trend toward
63 treatment, including reductions in risks of osteoporotic fracture and coronary heart disease, and th
64 ted whether MI constitutes a risk factor for osteoporotic fracture and examined secular trends in thi
65 erved for higher intake of flavonols for any osteoporotic fracture and major osteoporotic fracture, a
66 amined magnesium intake as a risk factor for osteoporotic fractures and altered bone mineral density
69 e-related disorder leading to an increase in osteoporotic fractures and resulting in significant suff
70 vity, prolonged corticosteroid use, previous osteoporotic fracture, and androgen deprivation therapy.
71 omen; 212 (17.8%) were identified as a major osteoporotic fracture, and of these, 129 (10.9%) were a
72 0-60% in persons with low bone mass or prior osteoporotic fracture, and SREs by one-third in cancer p
73 ncer risk factors, clinical risk factors for osteoporotic fractures, and bone mineral density surveil
74 D) is highly heritable, a major predictor of osteoporotic fractures, and has been previously associat
75 elderly white women enrolled in the Study of Osteoporotic Fractures, and initial breast cancer status
80 at BPs dispensed for secondary prevention of osteoporotic fractures are not associated with increased
81 nols for any osteoporotic fracture and major osteoporotic fracture, as well as flavones for hip fract
82 This study [B-vitamins for the PRevention Of Osteoporotic Fractures (B-PROOF)] aimed to determine whe
85 with adjudicated fracture outcomes (Study of Osteoporotic Fractures [December 1998-July 2008]; Osteop
86 rea under the curve (AUC) for incident major osteoporotic fracture discrimination (AUC: FRAX with BMD
91 [HR], 1.43 [95% CI, 1.16 to 1.78]) and major osteoporotic fracture (HR, 1.21 [95% CI, 1.01 to 1.45])
92 the highest tertile had a lower risk of any osteoporotic fracture (HR: 0.65; 95% CI: 0.47, 0.88), ma
93 acture (HR: 0.65; 95% CI: 0.47, 0.88), major osteoporotic fracture (HR: 0.66; 95% CI: 0.45, 0.95), an
94 iated with a 30% decrease in the risk of any osteoporotic fracture (HR: 0.70; 95% CI: 0.50, 0.96).
95 to LMWH) in 0.11% (95% CI, 0.02%-0.32%), and osteoporotic fracture in 0.04% (95% CI, < 0.01%-0.20%) o
96 ncreasing evidence suggests that the risk of osteoporotic fracture in adulthood could be determined p
97 risk factors for low bone mineral density or osteoporotic fracture in men or comparing 2 different me
100 ce in transfer are significant predictors of osteoporotic fracture in white female nursing home resid
101 The aims are to establish the prevalence of osteoporotic fractures in ISM and to investigate the ass
102 ation-based age-specific fracture rates; the Osteoporotic Fractures in Men (MrOS) study and published
103 n Older Men Study (an ancillary study to the Osteoporotic Fractures in Men (MrOS) Study conducted in
105 porotic Fractures [December 1998-July 2008]; Osteoporotic Fractures in Men Study [March 2000-March 20
107 d DHEA-S in the prospective population-based Osteoporotic Fractures in Men study in Sweden (2,416 men
108 In a cohort of 1,104 elderly men from the Osteoporotic Fractures in Men Study, 25(OH)D serum level
109 sical performance with incident falls in the Osteoporotic Fractures in Men Study, a large prospective
110 study of 2,865 participants derived from the Osteoporotic Fractures in Men Study, a prospective multi
113 to osteoporosis and to estimate the risk of osteoporotic fractures in relation to body weight, lean
116 B-12 and folic acid supplementation reduces osteoporotic fracture incidence in hyperhomocysteinemic
117 folic acid supplementation had no effect on osteoporotic fracture incidence in this elderly populati
118 ach of the studies and at each major site of osteoporotic fracture, including the hip and wrist.
120 assessed at the baseline Caregiver-Study of Osteoporotic Fractures interview, conducted in 1999-2001
125 ing health outcomes, including prevention of osteoporotic fractures, is essential for promoting the w
132 femoral neck) and an increased risk of both osteoporotic fractures (odds ratio [OR] 1.3, 95% CI 1.09
134 e of both risk alleles increased the risk of osteoporotic fractures (OR 1.3, 1.08-1.63, p=0.006) and
136 study population was drawn from the Study of Osteoporotic Fractures, Pittsburgh, Pennsylvania, during
139 roup analyses suggest a beneficial effect on osteoporotic fracture prevention in compliant persons ag
140 ificantly associated with the development of osteoporotic fractures (relative risk [RR] 2.5, 95% conf
143 or modulator) have each been shown to reduce osteoporotic fracture risk among men receiving androgen-
144 drugs available for these diseases, reducing osteoporotic fracture risk by 50-60% in persons with low
145 concentrations may be associated with lower osteoporotic fracture risk in older adults, particularly
146 sorders and psychotropic medication use with osteoporotic fracture risk in routine clinical practice.
148 ersons aged >80 y, in per-protocol analyses, osteoporotic fracture risk was lower in the intervention
150 Research shows that optimal screening for osteoporotic fracture risk will require risk factor info
151 hly heritable trait and a key determinant of osteoporotic fracture risk, but the genes responsible ar
152 as a clinical aid to assess an individual's osteoporotic fracture risk, with or without bone mineral
159 ociated with a small increase in the risk of osteoporotic fractures (RR 1.3, 95% CI 1.0, 1.8); howeve
161 men with DM; HRs for 1-unit increase in FRAX osteoporotic fracture score, 1.04; 95% CI, 1.02-1.05, fo
163 women ages > or = 65 years from the Study of Osteoporotic Fractures (SOF) and white men and women age
164 y community-dwelling women from the Study of Osteoporotic Fractures (SOF) cohort (mean age 83 years)
166 Pittsburgh Clinical Center for the Study of Osteoporotic Fractures (SOF), a prospective cohort study
167 the Pittsburgh Field Center of the Study of Osteoporotic Fractures (SOF), a prospective study of a c
169 aging needs to be used to diagnose prevalent osteoporotic fractures, such as spine fractures on chest
170 Despite African Americans' reduced risk of osteoporotic fractures, such fractures remain an importa
171 treatment to limit the enormous increase in osteoporotic fractures that has been predicted as the ag
173 In elderly men, who are at greatest risk for osteoporotic fracture, the influence of hypogonadism on
174 that many agents are effective in preventing osteoporotic fractures, the data are insufficient to det
176 We used data from the prospective Study of Osteoporotic Fractures to estimate risk of fracture from
178 Tool score, or FRAX), 10-year risk for major osteoporotic fracture was greater than 20% (FRAX), quant
181 ort of 5,552 elderly women from the Study of Osteoporotic Fractures was followed up prospectively for
184 We studied 5,839 women from the Study of Osteoporotic Fractures who had had serial pelvic radiogr
186 ith AFFs to those from patients with typical osteoporotic fractures with and without bisphosphonate t
188 > or =74 years participating in the Study of Osteoporotic Fractures year 10 follow-up (n = 906) in 19
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