Weight change, variability, and trajectories and risk of hip fracture among older adults with Dysglycemia: the cardiovascular health study.

IF 5.1 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Shohinee Sarma, Petra Bůžková, Rachel E Elam, Howard A Fink, Jane A Cauley, Luc Djoussé, Joshua Barzilay, Kenneth J Mukamal
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Abstract

Background: Type 2 diabetes mellitus and lower weight are both associated with osteoporotic fractures, but the roles of variability and trajectory are less clear.1 The associations of these factors among older adults with dysglycemia, who are at highest risk of fracture, with fracture risk and bone mineral density (BMD) remains uncertain.

Methods: We followed 775 men and 1080 women from the Cardiovascular Health Study (mean age 77.4 years) with abnormal oral glucose tolerance testing in 1989-1990. We measured their weights yearly through 1994-1995 and derived intra-individual mean weight, weight slope, and weight variability. We also used growth mixture modelling to derive four latent body-mass index trajectories over time. We used Cox proportional hazards models to calculate hazard ratios (HR) and 95% confidence intervals (CI) for subsequent hip fracture through 2015 and linear regression models to estimate cross-sectional associations with bone mineral density (BMD) of the hip.

Results: Each 10 kg higher mean weight was associated with a lower risk of subsequent hip fracture overall (HR 0.81; CI 0.70-0.94) and among women (HR 0.76; CI 0.64-0.91) and with higher BMD (P-value <0.001). Higher weight variability was directly associated with incident hip fracture among women (HR 1.18; CI: 1.03-1.35). Compared with a stable trajectory, a "progressive overweight" trajectory was associated with lower risk of hip fracture (HR 0.66; CI: 0.44-0.99). An uncommon trajectory of "accelerating obesity" was associated with higher BMD.

Conclusions: Among older adults with dysglycemia at high risk for fracture, lower mean weight is associated with higher fracture risk, but variability and trajectory may also contribute. These results highlight the complex effects of weight in older age.

患有糖耐量异常症的老年人的体重变化、可变性和轨迹与髋部骨折风险:心血管健康研究。
背景:2 型糖尿病和较低体重都与骨质疏松性骨折有关,但变异性和轨迹的作用却不太明确。1 在骨折风险最高的血糖异常老年人中,这些因素与骨折风险和骨矿物质密度(BMD)的关系仍不确定:我们对心血管健康研究(Cardiovascular Health Study)中的 775 名男性和 1080 名女性(平均年龄 77.4 岁)进行了跟踪调查,他们在 1989-1990 年期间的口服葡萄糖耐量测试均出现异常。我们在 1994-1995 年期间每年测量他们的体重,并得出了个体内部的平均体重、体重斜率和体重变异性。我们还使用生长混合模型得出了四个潜在体重指数随时间变化的轨迹。我们使用 Cox 比例危险模型计算了到 2015 年髋部骨折的危险比 (HR) 和 95% 置信区间 (CI),并使用线性回归模型估算了髋部骨矿物质密度 (BMD) 的横截面关联:结果:平均体重每增加 10 千克,髋部骨折发生风险总体降低(HR 0.81;CI 0.70-0.94),女性髋部骨折发生风险总体降低(HR 0.76;CI 0.64-0.91),BMD 增加(P-值 结论:髋部骨折发生风险总体降低(HR 0.81;CI 0.70-0.94),女性髋部骨折发生风险总体降低(HR 0.76;CI 0.64-0.91):在骨折风险较高的患有血糖异常的老年人中,较低的平均体重与较高的骨折风险相关,但可变性和轨迹也可能有所影响。这些结果凸显了体重对老年人的复杂影响。
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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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