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无早期慢性肾病和有早期慢性肾病个体的骨折预测工具比较:基于CARTaGENE人群的分析

Comparison of Fracture Prediction Tools in Individuals Without and With Early Chronic Kidney Disease: A Population-Based Analysis of CARTaGENE.

作者信息

Desbiens Louis-Charles, Sidibé Aboubacar, Beaudoin Claudia, Jean Sonia, Mac-Way Fabrice

机构信息

CHU de Québec Research Center, L'Hôtel-Dieu-de-Québec Hospital, Endocrinology and Nephrology Axis, Quebec City, Canada.

Department and Faculty of Medicine, Université Laval, Quebec City, Canada.

出版信息

J Bone Miner Res. 2020 Jun;35(6):1048-1057. doi: 10.1002/jbmr.3977. Epub 2020 Mar 10.

Abstract

Whether fracture prediction tools developed for the management of osteoporosis can be used in chronic kidney disease (CKD) is poorly known. We aimed to compare the performance of fracture prediction tools in non-CKD and CKD. We analyzed CARTaGENE, a population-based survey of 40-year-old to 69-year-old individuals recruited between 2009 and 2010. Renal function was assessed using baseline creatinine and categorized according to Kidney Disease Improving Global Outcomes (KDIGO) guidelines (non-CKD, stage 2, stage 3). Individuals without creatinine measurements or with advanced CKD (stage 4 or 5; prevalence <0.25%) were excluded. Predicted 5-year fracture probabilities (using Fracture Risk Assessment Tool [FRAX], QFracture, and Garvan) were computed at baseline. Fracture incidence (major fracture [MOF] or any fracture) was evaluated in administrative databases from recruitment to March 2016. Discrimination (hazard ratios [HRs] per standard deviation [SD] increase in Cox models; c-statistics) and calibration (standardized incidence ratios [SIRs] before and after recalibration) were assessed in each CKD strata. We included 19,393 individuals (9522 non-CKD; 9114 stage 2; 757 stage 3). A total of 830 patients had any fracture during follow-up, including 352 MOF. FRAX (HR = 1.89 [1.63-2.20] non-CKD; 1.64 [1.41-1.91] stage 2; 1.76 [1.10-2.82] stage 3) and QFracture (HR = 1.90 [1.62-2.22] non-CKD; 1.57 [1.35-1.82] stage 2; 1.86 [1.19-2.91] stage 3) discriminated MOF similarly in non-CKD and CKD. In contrast, the discrimination of Garvan for any fracture tended to be lower in CKD stage 3 compared to non-CKD and CKD stage 2 (HR = 1.36 [1.22-1.52] non-CKD; 1.34 [1.20-1.50] stage 2; 1.11 [0.79-1.55] stage 3). Before recalibration, FRAX globally overestimated fracture risk while QFracture and Garvan globally underestimated fracture risk. After recalibration, FRAX and QFracture were adequately calibrated for MOF in all CKD strata whereas Garvan tended to underestimate any fracture risk in CKD stage 3 (SIR = 1.31 [0.95-1.81]). In conclusion, the discrimination and calibration of FRAX and QFracture is similar in non-CKD and CKD. Garvan may have a lower discrimination in CKD stage 3 and underestimate fracture risk in these patients. © 2020 American Society for Bone and Mineral Research.

摘要

目前尚不清楚为骨质疏松症管理而开发的骨折预测工具是否可用于慢性肾脏病(CKD)。我们旨在比较骨折预测工具在非CKD和CKD中的性能。我们分析了CARTaGENE,这是一项基于人群的调查,调查对象为2009年至2010年招募的40岁至69岁个体。使用基线肌酐评估肾功能,并根据改善全球肾脏病预后组织(KDIGO)指南进行分类(非CKD、2期、3期)。排除没有肌酐测量值或患有晚期CKD(4期或5期;患病率<0.25%)的个体。在基线时计算预测的5年骨折概率(使用骨折风险评估工具[FRAX]、QFracture和Garvan)。在从招募到2016年3月的行政数据库中评估骨折发生率(主要骨折[MOF]或任何骨折)。在每个CKD分层中评估辨别力(Cox模型中每标准差[SD]增加的风险比[HRs];c统计量)和校准(重新校准前后的标准化发病率比[SIRs])。我们纳入了19393名个体(9522名非CKD;9114名2期;757名3期)。共有830名患者在随访期间发生了任何骨折,包括352例MOF。FRAX(HR = 1.89 [1.63 - 2.20]非CKD;1.64 [1.41 - 1.91] 2期;1.76 [1.10 - 2.82] 3期)和QFracture(HR = 1.90 [1.62 - 2.22]非CKD;1.57 [1.35 - 1.82] 2期;1.86 [1.19 - 2.91] 3期)在非CKD和CKD中对MOF的辨别力相似。相比之下,与非CKD和CKD 2期相比,Garvan对任何骨折的辨别力在CKD 3期往往较低(HR = 1.36 [1.22 - 1.52]非CKD;1.34 [1.20 - 1.50] 2期;1.11 [0.79 - 1.55] 3期)。在重新校准之前,FRAX总体上高估了骨折风险,而QFracture和Garvan总体上低估了骨折风险。重新校准后,FRAX和QFracture在所有CKD分层中对MOF进行了充分校准,而Garvan在CKD 3期往往低估了任何骨折风险(SIR = 1.31 [0.95 - 1.81])。总之,FRAX和QFracture在非CKD和CKD中的辨别力和校准相似。Garvan在CKD 3期可能辨别力较低,并低估了这些患者的骨折风险。© 2020美国骨与矿物质研究学会。

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