1997
DOI: 10.1016/s0378-5122(97)88490-3
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Low bone mass and fast rate of bone loss at menopause: equal risk factors for future fracture. A 15-year follow-up study

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Cited by 62 publications
(88 citation statements)
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“…[64][65][66] BMD is a function of peak bone mass and the rate of subsequent bone loss, which are risk factors for fracture later in life. 66 Thus, an intervention in childhood to maximize peak bone mass in high-risk individuals could have potential long-term beneficial effects in adults by minimizing the impact of later bone loss.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…[64][65][66] BMD is a function of peak bone mass and the rate of subsequent bone loss, which are risk factors for fracture later in life. 66 Thus, an intervention in childhood to maximize peak bone mass in high-risk individuals could have potential long-term beneficial effects in adults by minimizing the impact of later bone loss.…”
Section: Discussionmentioning
confidence: 99%
“…[64][65][66] BMD is a function of peak bone mass and the rate of subsequent bone loss, which are risk factors for fracture later in life. 66 Thus, an intervention in childhood to maximize peak bone mass in high-risk individuals could have potential long-term beneficial effects in adults by minimizing the impact of later bone loss. 67 As the costs of osteoporosis and related fractures currently exceed $6 billion per year in the United States, 68,69 successful interventions could have substantial economic implications.…”
Section: Discussionmentioning
confidence: 99%
“…Estrogen deficiency at menopause induces a phase of rapid bone loss over 5 to 10 years that is prevented by exogenous estrogen therapy [34]. Postmenopausal bone loss is associated with an increased bone turnover, reflected by an increase in biochemical markers of bone turnover [24,59]. In a large cohort of healthy and ambulatory elderly women, the levels of serum estradiol (E2) and sex hormone-binding globulin (SHBG) were predictors of hip fracture, but this association was dependent on body weight [7].…”
Section: Discussionmentioning
confidence: 99%
“…(4) Urinary cross-link excretion, especially deoxypyridinoline, correlates with bone turnover in patients with vertebral osteoporosis (7,8) and fracture risk. (9,10) These markers are now being used to assess efficacy of treatment for metabolic bone diseases (11)(12)(13)(14)(15) and fracture risk. (9,10,16) Osteocalcin is a low molecular weight protein produced by active osteoblasts during bone formation.…”
Section: Introductionmentioning
confidence: 99%
“…(9,10) These markers are now being used to assess efficacy of treatment for metabolic bone diseases (11)(12)(13)(14)(15) and fracture risk. (9,10,16) Osteocalcin is a low molecular weight protein produced by active osteoblasts during bone formation. It is incorporated primarily into the mineralizing matrix, but a small amount is released into circulation.…”
Section: Introductionmentioning
confidence: 99%