Height loss in older women: risk of hip fracture and mortality independent of vertebral fractures.
Height loss in older women: risk of hip fracture and mortality independent of vertebral fractures.
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DOI:
10.1002/jbmr.558
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发表时间:
2012-01
影响因子:
6.2
通讯作者:
Cummings, Steven R.
中科院分区:
文献类型:
--
作者:
Hillier, Teresa A.;Lui, Li-Yung;Kado, Deborah M.;LeBlanc, E. S.;Vesco, Kimberly K.;Bauer, Douglas C.;Cauley, Jane A.;Ensrud, Kristine E.;Black, Dennis M.;Hochberg, Marc C.;Cummings, Steven R.
We examined if height loss in older women predicts risk of hip fractures, other non-spine fractures, and mortality, and whether this risk is independent of both vertebral fractures (VFx) and bone mineral density (BMD) by dual-energy x-ray absorptiometry. Among 3,124 women age 65 and older in the Study of Osteoporotic Fractures, we assessed the association with measured height change between Year 0 (1986–1988) and Year 15 (2002–2004) and subsequent risk of radiologically confirmed hip fractures, other non-spine fractures, and mortality assessed via death certificates. Follow-up occurred every 4 months for fractures and vital status (>95% contacts complete). Cox proportional hazards models assessed risk of hip fracture, non-spine fracture, and mortality over a mean of 5 years after height change was assessed (i.e, after final height measurement). After adjustment for VFx, BMD and other potential covariates, height loss >5 cm was associated with a marked increased risk of hip fracture (HR 1.50, 95% CI 1.06, 2.12), non-spine fracture (HR 1.48; 95% CI 1.20, 1.83), and mortality (1.45; 95% CI 1.21, 1.73). Although primary analyses were a subset of 3,124 survivors healthy enough to return for a Year 15 height measurement, a sensitivity analysis in the entire cohort (n=9,677) using initial height in earlier adulthood (self-reported height at age 25 [−40 years] to measured height age >65 years [Year 0]) demonstrated consistent results. Height loss >5 cm (2”) in older women was associated with a nearly 50% increased risk of hip fracture, non-spine fracture, and mortality—independent of incident VFx and BMD.
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影响因子:
39.2
作者:
Kado DM;Lui LY;Ensrud KE;Fink HA;Karlamangla AS;Cummings SR;Study of Osteoporotic Fractures
通讯作者:
Study of Osteoporotic Fractures
影响因子:
6.2
作者:
Moayyeri, Alireza;Luben, Robert N.;Khaw, Kay-Tee
通讯作者:
Khaw, Kay-Tee
影响因子:
6.1
作者:
Baron, YM;Brincat, MP;Calleja, N
通讯作者:
Calleja, N
影响因子:
--
作者:
Hillier, Teresa A.;Stone, Katie L.;Cummings, Steve R.
通讯作者:
Cummings, Steve R.
影响因子:
6.2
作者:
Black, DM;Arden, NK;Cummings, SR
通讯作者:
Cummings, SR