无骨密度FRAX预测多种族糖尿病患者骨折风险的偏差:糖尿病与老龄化研究

IF 6.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Bone and Mineral Research Pub Date : 2025-04-21 DOI:10.1093/jbmr/zjaf012
Rajesh K Jain, Jennifer Y Liu, Richard W Grant, Shanzay Haider, Elbert S Huang, Neda Laiteerapong, Kasia J Lipska, Joan C Lo, Howard H Moffet, Melissa M Parker, Andrew J Karter
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引用次数: 0

摘要

骨折风险计算器,如骨折风险评估工具(FRAX),计算严重骨质疏松症(MOF)和髋部骨折的风险,但不考虑糖尿病患者的过度骨折风险。我们在不同种族的老年糖尿病患者中检测了不含BMD的FRAX的预测性能。纳入的患者年龄在65-89岁之间,来自Kaiser Permanente北加州糖尿病登记,并且没有服用骨质疏松药物。种族和民族都是自我认定的。我们根据基线特征计算了不含骨密度的FRAX,并评估了FRAX在随访中对MOF和髋部骨折的预测效果。预测性能是基于辨别(接收器操作曲线下面积,AUC)和校准(观察到的预测比,O/P)的测量。我们确定了96914例患者(47.0%为女性),其中5383例(5.6%)和1767例(1.8%)分别患有MOF和髋部骨折,平均随访时间为4.3年。MOF和髋部骨折的AUC分别为0.72和0.77。总体而言,FRAX略微低估了MOF和髋部骨折的发生率(两者的O/P均为1.2)。种族、民族和糖尿病病程的歧视相似,但在75岁以上(AUC)的人群中更严重
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Biases in the performance of FRAX without BMD in predicting fracture risk in a multiethnic population with diabetes: the Diabetes and Aging Study.

Fracture risk calculators, such as the Fracture Risk Assessment Tool (FRAX), calculate the risk of major osteoporotic fracture (MOF) and hip fracture but do not account for the excess risk of fracture in people with diabetes. We examined the predictive performance of FRAX without BMD in ethnically diverse, older patients with diabetes. Patients included were between ages 65 and 89 from the Kaiser Permanente Northern California Diabetes Registry and not already taking osteoporosis medications. Race and ethnicity were self-identified. We calculated FRAX without BMD based on baseline characteristics and assessed how well FRAX predicted MOF and hip fracture over follow-up. Predictive performance was based on measures of discrimination (area under the receiver operator curve, AUC) and calibration (observed-to-predicted ratio, O/P). We identified 96 914 patients (47.0% female), of whom 5383 (5.6%) and 1767 (1.8%) had MOF and hip fracture, respectively, over a mean follow-up of 4.3 yr. The AUC for MOF and hip fracture were 0.72 and 0.77, respectively. FRAX mildly underestimated MOF and hip fracture rates (O/P 1.2 for both) overall. Discrimination was similar by race and ethnicity and diabetes duration but was worse in those over age 75 (AUC < 0.7). In some groups, there were substantial calibration errors, such as Hispanic women (O/P: 1.8 and 1.5), Black men (O/P: 1.5 and 1.8), those with duration of diabetes ≥20 yr (O/P: 1.6 and 1.5), and those over the age of 80 (O/P: 1.4 and 1.2) for MOF and hip fracture, respectively. While the discriminatory performance of FRAX without BMD was good overall in patients with diabetes, it underestimated risk in Hispanic women, Black men, those with long duration of diabetes, and in the oldest patients with diabetes. These algorithmic biases suggest that diabetes-specific tools may be needed to stratify fracture risk in patients with diabetes.

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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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