Fracture Risk Prediction in Patients Receiving Dialysis.

IF 6.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Andrea C J Cowan, Yuguang Kang, Stephanie N Dixon, Nivethika Jeyakumar, Jessica M Sontrop, Kristin K Clemens, Amit X Garg
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Abstract

Patients receiving dialysis face a 5-fold higher risk of skeletal fractures compared to the general population, along with increased mortality and a longer hospital stay after a fracture. However, fracture risk varies among patients, and reliable methods to assess risk are limited. Using linked healthcare databases, we conducted a population-based cohort study of adults aged 40-90 years receiving maintenance dialysis with an available parathyroid hormone (PTH) value in Ontario, Canada (2010-2017). Patients were followed for 3 years or until death, first major fracture, or provincial emigration. Using Fine and Gray subdistribution hazards models accounting for the competing risk of death, we developed a fracture prediction tool (Dial-Frac) that included demographic, comorbidity, and laboratory information. Models were compared using measures of discrimination, calibration, and model fit and were internally validated using 10-fold cross-validation. The cohort included 11,599 patients receiving dialysis. Mean age was 66 years; 39% were female, and 12% had a previous fracture. Over 3 years, 839 patients (7.2%) experienced a fracture (44% of which occurred in the first year); hip fracture was most common (299/839). The final prediction model included age, sex, previous fracture, previous kidney transplant, proton pump inhibitor use, and PTH and serum albumin concentrations. The time dependent area under the receiver operating curve for fracture at 1 and 3 years were 0.79 and 0.71, respectively, indicating good discrimination. We developed Dial-Frac, an easy-to-implement equation that predicts fracture risk in patients receiving maintenance dialysis. It predicts risk at 1 and 3 years without requiring bone density measurements or additional tests, helping to identify high-risk patients for further screening, preventive interventions and clinical trial participation. Next steps include external validation.

透析患者骨折风险预测。
与一般人群相比,接受透析的患者患骨骼骨折的风险要高出5倍,同时死亡率也会增加,骨折后住院时间也会更长。然而,骨折风险因患者而异,评估风险的可靠方法有限。使用相关的医疗数据库,我们在加拿大安大略省(2010-2017)进行了一项基于人群的队列研究,研究对象为接受维持性透析的40-90岁成年人,并测量甲状旁腺激素(PTH)值。患者随访3年或至死亡、首次严重骨折或外省移民。使用Fine和Gray亚分布风险模型来考虑死亡的竞争风险,我们开发了一种骨折预测工具(Dial-Frac),包括人口统计、合并症和实验室信息。采用判别、校准和模型拟合的方法对模型进行比较,并采用10倍交叉验证进行内部验证。该队列包括11,599名接受透析的患者。平均年龄66岁;其中39%为女性,12%有过骨折史。3年多来,839例患者(7.2%)发生骨折(其中44%发生在第一年);髋部骨折最为常见(299/839)。最终的预测模型包括年龄、性别、既往骨折、既往肾移植、质子泵抑制剂使用、甲状旁腺激素和血清白蛋白浓度。1年和3年骨折受术者操作曲线下的时间依赖面积分别为0.79和0.71,具有较好的判别性。我们开发了Dial-Frac,这是一个易于实现的方程,可以预测接受维持性透析的患者骨折风险。它可以预测1年和3年的风险,而不需要骨密度测量或其他测试,有助于识别高风险患者,进行进一步筛查、预防性干预和临床试验参与。接下来的步骤包括外部验证。
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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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