Predictive Performance of Established Cardiovascular Risk Scores in the Prediabetic Population: External Validation using the UK Biobank Dataset

Prediabetes is a highly heterogenous metabolic state with increased risk of cardiovascular disease (CVD). Current guidelines raised the necessity of CVD risk scoring for prediabetes without clear recommendations. Thus, this study aimed to systematically assess the performance of 11 models, including...

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Veröffentlicht in:European journal of preventive cardiology 2023-04
Hauptverfasser: Li, Miaohong, Lin, Yifen, Zhong, Xiangbin, Huang, Rihua, Zhang, Shaozhao, Liu, Menghui, Liu, Sen, Ye, Xiaomin, Xu, Xinghao, Huang, Yiquan, Xiong, Zhenyu, Guo, Yue, Liao, Xinxue, Zhuang, Xiaodong
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container_title European journal of preventive cardiology
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creator Li, Miaohong
Lin, Yifen
Zhong, Xiangbin
Huang, Rihua
Zhang, Shaozhao
Liu, Menghui
Liu, Sen
Ye, Xiaomin
Xu, Xinghao
Huang, Yiquan
Xiong, Zhenyu
Guo, Yue
Liao, Xinxue
Zhuang, Xiaodong
description Prediabetes is a highly heterogenous metabolic state with increased risk of cardiovascular disease (CVD). Current guidelines raised the necessity of CVD risk scoring for prediabetes without clear recommendations. Thus, this study aimed to systematically assess the performance of 11 models, including five general population-based and six diabetes-specific CVD risk scores, in prediabetes. A cohort of individuals aged 40-69 years with prediabetes (HbA1c ≥ 5.7 and
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Current guidelines raised the necessity of CVD risk scoring for prediabetes without clear recommendations. Thus, this study aimed to systematically assess the performance of 11 models, including five general population-based and six diabetes-specific CVD risk scores, in prediabetes. A cohort of individuals aged 40-69 years with prediabetes (HbA1c ≥ 5.7 and &lt;6.5%) and without baseline CVD or known diabetes was identified from the UK Biobank, which was used to validate 11 prediction models for estimating 10-year or 5-year risk of CVD. Model discrimination and calibration were evaluated by Harrell's C-statistic and calibration plots, respectively. We further performed decision curve analyses to assess the clinical usefulness.Overall, 56,831 prediabetic individuals were included, of which 4,303 incident CVD events occurred within a median follow-up of 8.9 years. All the 11 risk scores assessed had modest C-statistics for discrimination ranging from 0.647 to 0.680 in prediabetes. Scores developed in the general population did not outperform those diabetes-specific models (C-statistics 0.647-0.675 vs. 0.647-0.680), while the PREDICT-1° Diabetes equation developed for type 2 diabetes performed best [0.680 (95% confidence interval 0.672-0.689)]. The calibration plots suggested overall poor calibration except that the PREDICT-1° Diabetes equation calibrated well after recalibration. The decision curves generally indicated moderate clinical usefulness of each model, especially worse within high threshold probabilities. Neither risk stratification schemes for the general population nor those specific for type 2 diabetes performed well in the prediabetic population. The PREDICT-1° Diabetes equation could be a substitute in the absence of better alternatives, rather than the general population-based scores. 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Current guidelines raised the necessity of CVD risk scoring for prediabetes without clear recommendations. Thus, this study aimed to systematically assess the performance of 11 models, including five general population-based and six diabetes-specific CVD risk scores, in prediabetes. A cohort of individuals aged 40-69 years with prediabetes (HbA1c ≥ 5.7 and &lt;6.5%) and without baseline CVD or known diabetes was identified from the UK Biobank, which was used to validate 11 prediction models for estimating 10-year or 5-year risk of CVD. Model discrimination and calibration were evaluated by Harrell's C-statistic and calibration plots, respectively. We further performed decision curve analyses to assess the clinical usefulness.Overall, 56,831 prediabetic individuals were included, of which 4,303 incident CVD events occurred within a median follow-up of 8.9 years. All the 11 risk scores assessed had modest C-statistics for discrimination ranging from 0.647 to 0.680 in prediabetes. Scores developed in the general population did not outperform those diabetes-specific models (C-statistics 0.647-0.675 vs. 0.647-0.680), while the PREDICT-1° Diabetes equation developed for type 2 diabetes performed best [0.680 (95% confidence interval 0.672-0.689)]. The calibration plots suggested overall poor calibration except that the PREDICT-1° Diabetes equation calibrated well after recalibration. The decision curves generally indicated moderate clinical usefulness of each model, especially worse within high threshold probabilities. Neither risk stratification schemes for the general population nor those specific for type 2 diabetes performed well in the prediabetic population. The PREDICT-1° Diabetes equation could be a substitute in the absence of better alternatives, rather than the general population-based scores. 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Current guidelines raised the necessity of CVD risk scoring for prediabetes without clear recommendations. Thus, this study aimed to systematically assess the performance of 11 models, including five general population-based and six diabetes-specific CVD risk scores, in prediabetes. A cohort of individuals aged 40-69 years with prediabetes (HbA1c ≥ 5.7 and &lt;6.5%) and without baseline CVD or known diabetes was identified from the UK Biobank, which was used to validate 11 prediction models for estimating 10-year or 5-year risk of CVD. Model discrimination and calibration were evaluated by Harrell's C-statistic and calibration plots, respectively. We further performed decision curve analyses to assess the clinical usefulness.Overall, 56,831 prediabetic individuals were included, of which 4,303 incident CVD events occurred within a median follow-up of 8.9 years. All the 11 risk scores assessed had modest C-statistics for discrimination ranging from 0.647 to 0.680 in prediabetes. Scores developed in the general population did not outperform those diabetes-specific models (C-statistics 0.647-0.675 vs. 0.647-0.680), while the PREDICT-1° Diabetes equation developed for type 2 diabetes performed best [0.680 (95% confidence interval 0.672-0.689)]. The calibration plots suggested overall poor calibration except that the PREDICT-1° Diabetes equation calibrated well after recalibration. The decision curves generally indicated moderate clinical usefulness of each model, especially worse within high threshold probabilities. Neither risk stratification schemes for the general population nor those specific for type 2 diabetes performed well in the prediabetic population. The PREDICT-1° Diabetes equation could be a substitute in the absence of better alternatives, rather than the general population-based scores. 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title Predictive Performance of Established Cardiovascular Risk Scores in the Prediabetic Population: External Validation using the UK Biobank Dataset
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