Development and validation of a lifetime prediction model for incident type 2 diabetes in patients with established cardiovascular disease: the CVD2DM model

被引:2
作者
Helmink, Marga A. G. [1 ]
Peters, Sanne A. E. [2 ,3 ,4 ]
Westerink, Jan [1 ,5 ]
Harris, Katie [4 ]
Tillmann, Taavi [6 ]
Woodward, Mark [3 ,4 ]
van Sloten, Thomas T. [1 ]
van der Meer, Manon G. [7 ]
Teraa, Martin [8 ]
Dorresteijn, Jannick A. N. [1 ]
Ruigrok, Ynte M. [9 ]
Visseren, Frank L. J. [1 ]
Hageman, Steven H. J. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Vasc Med, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[2] Univ Utrecht, Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[3] Imperial Coll London, George Inst Global Hlth, London, England
[4] Univ New South Wales, George Inst Global Hlth, Sydney, NSW, Australia
[5] Isala, Dept Internal Med, Zwolle, Netherlands
[6] Univ Tartu, Inst Family Med & Publ Hlth, Tartu, Estonia
[7] Univ Med Ctr Utrecht, Dept Cardiol, Utrecht, Netherlands
[8] Univ Med Ctr Utrecht, Dept Vasc Surg, Utrecht, Netherlands
[9] Univ Med Ctr Utrecht, Dept Neurol, Utrecht, Netherlands
关键词
Cardiovascular disease; Type; 2; diabetes; Risk prediction; Prevention; RISK; MELLITUS; ADULTS; STYLE; TOOL;
D O I
10.1093/eurjpc/zwae096
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Identifying patients with established cardiovascular disease (CVD) who are at high risk of type 2 diabetes (T2D) may allow for early interventions, reducing the development of T2D and associated morbidity. The aim of this study was to develop and externally validate the CVD2DM model to estimate the 10-year and lifetime risks of T2D in patients with established CVD.Methods and results Sex-specific, competing risk-adjusted Cox proportional hazard models were derived in 19 281 participants with established CVD and without diabetes at baseline from the UK Biobank. The core model's pre-specified predictors were age, current smoking, family history of diabetes mellitus, body mass index, systolic blood pressure, fasting plasma glucose, and HDL cholesterol. The extended model also included HbA1c. The model was externally validated in 3481 patients from the UCC-SMART study. During a median follow-up of 12.2 years (interquartile interval 11.3-13.1), 1628 participants with established CVD were diagnosed with T2D in the UK Biobank. External validation c-statistics were 0.79 [95% confidence interval (CI) 0.76-0.82] for the core model and 0.81 (95% CI 0.78-0.84) for the extended model. Calibration plots showed agreement between predicted and observed 10-year risk of T2D.Conclusion The 10-year and lifetime risks of T2D can be estimated with the CVD2DM model in patients with established CVD, using readily available clinical predictors. The model would benefit from further validation across diverse ethnic groups to enhance its applicability. Informing patients about their T2D risk could motivate them further to adhere to a healthy lifestyle. In this study, we developed and externally validated the CVD2DM model, which predicts the 10-year and lifetime risk of type 2 diabetes (T2D) in individuals who already have cardiovascular disease (CVD). The key findings are as follows: The CVD2DM model is the first model to estimate the risk of developing T2D applicable in all patients with atherosclerotic CVD. The model is based on several factors available in clinical practice, such as age, fasting plasma glucose, family history of diabetes, and body mass index. It was developed in 19 281 patients from the UK Biobank. The model performed well in 3481 patients from the UCC-SMART study.Informing patients about their T2D risk could motivate them further to adhere to a healthy lifestyle.
引用
收藏
页码:1671 / 1678
页数:8
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