TY - JOUR
T1 - Prediction of 10-year vascular risk in patients with diabetes
T2 - The AD-ON risk score
AU - on behalf of the ADVANCE Collaborative Group
AU - Woodward, M.
AU - Hirakawa, Y.
AU - Kengne, A. P.
AU - Matthews, D. R.
AU - Zoungas, S.
AU - Patel, A.
AU - Poulter, N.
AU - Grobbee, R.
AU - Cooper, M.
AU - Jardine, M.
AU - Chalmers, J.
N1 - Funding Information:
The ADVANCE-ON trial was supported by grants from the National Health and Medical Research Council of Australia (1006367, 358395, and 571281), a joint grant from Diabetes UK and the British Heart Foundation (28562), and an unrestricted educational grant from Servier International.
Publisher Copyright:
© 2016 John Wiley & Sons Ltd.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Aims: To formulate a combined cardiovascular risk score in diabetes that could be useful both to physicians and healthcare funders. Methods: Data were derived from the Action in Diabetes and Vascular Disease: Preterax and Diamicron Modified Release Controlled Evaluation Observational (ADVANCE-ON) study, a randomized controlled trial (mean duration 5years) with a post-randomization follow-up (mean 4.9years), that included 11140 high-risk patients with diabetes. The outcome analysed was the occurrence of either fatal or non-fatal macrovascular or renal disease. A Cox regression model was used to determine weightings in the risk score. The resultant score was recalibrated to each of three major global regions, as covered by the ADVANCE-ON study. Results: Over a median of 9.9years, 1145 patients experienced at least one component of the combined outcome event. The resultant score, the AD-ON risk score, incorporated 13 demographic or clinical variables. Its discrimination was modest [c-statistic=0.668 (95% confidence interval 0.651, 0.685)] but its calibration was excellent (predicted and observed risks coincided well, within disparate global regions). In terms of the integrated discrimination improvement index, its performance was marginally superior, over a 10-year risk horizon, to existing risk scores in clinical use, from a restricted version of the same data, for macrovascular and renal disease separately. Conclusions: The AD-ON risk score has advantages over the existing vascular risk scores in diabetes that used data from the original ADVANCE trial, which treat macrovascular and renal diseases separately. These advantages include its simplicity of use and global application.
AB - Aims: To formulate a combined cardiovascular risk score in diabetes that could be useful both to physicians and healthcare funders. Methods: Data were derived from the Action in Diabetes and Vascular Disease: Preterax and Diamicron Modified Release Controlled Evaluation Observational (ADVANCE-ON) study, a randomized controlled trial (mean duration 5years) with a post-randomization follow-up (mean 4.9years), that included 11140 high-risk patients with diabetes. The outcome analysed was the occurrence of either fatal or non-fatal macrovascular or renal disease. A Cox regression model was used to determine weightings in the risk score. The resultant score was recalibrated to each of three major global regions, as covered by the ADVANCE-ON study. Results: Over a median of 9.9years, 1145 patients experienced at least one component of the combined outcome event. The resultant score, the AD-ON risk score, incorporated 13 demographic or clinical variables. Its discrimination was modest [c-statistic=0.668 (95% confidence interval 0.651, 0.685)] but its calibration was excellent (predicted and observed risks coincided well, within disparate global regions). In terms of the integrated discrimination improvement index, its performance was marginally superior, over a 10-year risk horizon, to existing risk scores in clinical use, from a restricted version of the same data, for macrovascular and renal disease separately. Conclusions: The AD-ON risk score has advantages over the existing vascular risk scores in diabetes that used data from the original ADVANCE trial, which treat macrovascular and renal diseases separately. These advantages include its simplicity of use and global application.
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U2 - 10.1111/dom.12614
DO - 10.1111/dom.12614
M3 - Article
C2 - 26661693
AN - SCOPUS:84957847630
SN - 1462-8902
VL - 18
SP - 289
EP - 294
JO - Diabetes, Obesity and Metabolism
JF - Diabetes, Obesity and Metabolism
IS - 3
ER -