External validation and calibration of risk equations for prediction of diabetic kidney diseases among patients with type 2 diabetes in Taiwan.

IF 8.5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiovascular Diabetology Pub Date : 2024-10-09 DOI:10.1186/s12933-024-02443-4
Hsuan-Yu Su, Thi Thuy Dung Nguyen, Wei-Hung Lin, Huang-Tz Ou, Shihchen Kuo
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Abstract

Background: Most existing risk equations for predicting/stratifying individual diabetic kidney disease (DKD) risks were developed using relatively dated data from selective and homogeneous trial populations comprising predominately Caucasian type 2 diabetes (T2D) patients. We seek to adapt risk equations for prediction of DKD progression (microalbuminuria, macroalbuminuria, and renal failure) using empiric data from a real-world population with T2D in Taiwan.

Methods: Risk equations from three well-known simulation models: UKPDS-OM2, RECODe, and CHIME models, were adapted. Discrimination and calibration were determined using the area under the receiver operating characteristic curve (AUROC), a calibration plot (slope and intercept), and the Greenwood-Nam-D'Agostino (GND) test. Recalibration was performed for unsatisfactory calibration (p-value of GND test < 0.05) by adjusting the baseline hazards of risk equations to address risk variations among patients.

Results: The RECODe equations for microalbuminuria and macroalbuminuria showed moderate discrimination (AUROC: 0.62 and 0.76) but underestimated the event risks (calibration slope > 1). The CHIME equation had the best discrimination for renal failure (AUROCs from CHIME, UKPDS-OM2 and RECODe: 0.77, 0.60 and 0.64, respectively). All three equations overestimated renal failure risk (calibration slope < 1). After rigorous updating, the calibration slope/intercept of the recalibrated RECODe for predicting microalbuminuria (0.87/0.0459) and macroalbuminuria (1.10/0.0004) risks as well as the recalibrated CHIME equation for predicting renal failure risk (0.95/-0.0014) were improved.

Conclusions: Risk equations for prediction of DKD progression in real-world Taiwanese T2D patients were established, which can be incorporated into a multi-state simulation model to project and differentiate individual DKD risks for supporting timely interventions and health economic research.

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用于预测台湾 2 型糖尿病患者糖尿病肾脏疾病的风险方程的外部验证和校准。
背景:现有的用于预测/分级个体糖尿病肾病(DKD)风险的大多数风险方程都是利用来自以白种人为主的 2 型糖尿病(T2D)患者的选择性同质试验人群的相对过时的数据开发的。我们试图利用台湾真实世界中 T2D 患者的经验数据,调整预测 DKD 进展(微量白蛋白尿、大量白蛋白尿和肾衰竭)的风险方程:方法:三个著名模拟模型中的风险方程:方法:改编了 UKPDS-OM2、RECODe 和 CHIME 模型中的风险方程。使用接收者操作特征曲线下面积(AUROC)、校准图(斜率和截距)和格林伍德-南-达戈斯蒂诺(GND)测试确定识别和校准。如果校准结果不理想(GND 检验结果的 p 值),则进行重新校准:微量白蛋白尿和宏观白蛋白尿的 RECODe 方程显示出中等程度的区分度(AUROC:0.62 和 0.76),但低估了事件风险(校准斜率 > 1)。CHIME 方程对肾衰竭的判别能力最强(CHIME、UKPDS-OM2 和 RECODe 的 AUROC 分别为 0.77、0.60 和 0.64)。所有三个方程都高估了肾功能衰竭风险(校准斜率):建立了预测台湾 T2D 患者 DKD 进展的风险方程,可将其纳入多状态模拟模型,预测和区分个体 DKD 风险,以支持及时干预和卫生经济学研究。
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来源期刊
Cardiovascular Diabetology
Cardiovascular Diabetology 医学-内分泌学与代谢
CiteScore
12.30
自引率
15.10%
发文量
240
审稿时长
1 months
期刊介绍: Cardiovascular Diabetology is a journal that welcomes manuscripts exploring various aspects of the relationship between diabetes, cardiovascular health, and the metabolic syndrome. We invite submissions related to clinical studies, genetic investigations, experimental research, pharmacological studies, epidemiological analyses, and molecular biology research in this field.
期刊最新文献
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