Premenopausal and early postmenopausal trabecular bone score (TBS) and fracture risk: Study of Women's Health Across the Nation (SWAN)

被引:11
作者
Greendale, Gail A. [1 ]
Huang, MeiHua [1 ]
Cauley, Jane A. [2 ]
Harlow, Sioban [3 ]
Finkelstein, Joel S. [4 ]
Karlamangla, Arun S. [1 ]
机构
[1] Univ Calif Los Angeles, Div Geriatr, Dept Med, 10945 Le Conte Ave,Suite 2339, Los Angeles, CA 90095 USA
[2] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Epidemiol, Crabtree Hall A547,130 DeSoto St, Pittsburgh, PA 15261 USA
[3] Univ Michigan, Sch Publ Hlth, Dept Epidemiol, 1415 Washington Hts,Room 6618, Ann Arbor, MI 48109 USA
[4] Massachusetts Gen Hosp, Dept Med, Endocrine Unit, 50 Blossom St, Boston, MA 02114 USA
关键词
Menopause; Trabecular bone score; Epidemiology; Cohort; Longitudinal; MINERAL DENSITY; OSTEOPOROTIC FRACTURES; PREDICTION; COHORT; BMD;
D O I
10.1016/j.bone.2020.115543
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Evidence that trabecular bone score (TBS), an index of bone microstructure, is a risk factor for future fracture comes mainly from studies of late postmenopausal women. Objective: To discern whether premenopausal TBS or early postmenopausal TBS predict fracture. Design: A 22-year, prospective analysis from the Study of Women's Health Across Nation. Setting: Community-based cohort. Participants: 272 Black, 174 Japanese, and 364 White women. Main outcome measures: Incident fractures: 292 in premenopausal sample and 141 in early postmenopausal sample. Results: Separate Cox proportional hazard regressions modeled time to incident fracture as a function of TBS measured during premenopause or early postmenopause. Models were initially adjusted for age, race/ethnicity, SWAN clinical site, body mass index, use of calcium, vitamin D, bone beneficial or bone adverse medication. Next, we added lumbar spine (LS) or femoral neck (FN) bone mineral density (BMD) and, finally, history of prior fracture, to the models. For each standard deviation decrement in premenopausal TBS, fracture hazard was elevated by 17% (relative hazard [RH] 1.17 [95% CI, 1.02-1.35]); after adjusting for LS or FN BMD, the relation between premenopausal TBS and fracture was no longer statistically significant. There was a similar-magnitude, marginally statistically significant, association between early postmenopausal TBS and fracture, unadjusted for BMD (RH 1.15 [0.95-1.39]). Conclusions: Variation in premenopausal TBS is related to fracture risk, but this association is not independent of BMD.
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页数:7
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