Development and validation of Risk Equations for Complications Of type 2 Diabetes (RECODe) using individual participant data from randomised trials

被引:140
作者
Basu, Sanjay [1 ,2 ,3 ,4 ]
Sussman, Jeremy B. [8 ,9 ]
Berkowitz, Seth A. [5 ,6 ,7 ]
Hayward, Rodney A. [8 ,9 ]
Yudkin, John S. [10 ]
机构
[1] Stanford Univ, Ctr Populat Hlth Sci, Ctr Primary Care & Outcomes Res, Palo Alto, CA 94304 USA
[2] Stanford Univ, Dept Med, Palo Alto, CA 94304 USA
[3] Stanford Univ, Dept Hlth Res & Policy, Palo Alto, CA 94304 USA
[4] Harvard Med Sch, Ctr Primary Care, Boston, MA USA
[5] Harvard Med Sch, Dept Med, Boston, MA USA
[6] Massachusetts Gen Hosp, Div Gen Internal Med, Boston, MA 02114 USA
[7] Massachusetts Gen Hosp, Diabet Unit, Boston, MA 02114 USA
[8] Univ Michigan, Div Gen Med, Ann Arbor, MI 48109 USA
[9] Vet Affairs Ann Arbor Healthcare, Ctr Clin Management Res, Ann Arbor, MI USA
[10] UCL, Inst Cardiovasc Sci, Div Med, London, England
基金
美国国家卫生研究院;
关键词
CARDIOVASCULAR OUTCOMES; CALIBRATION; MORTALITY; MODEL;
D O I
10.1016/S2213-8587(17)30221-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background In view of substantial mis-estimation of risks of diabetes complications using existing equations, we sought to develop updated Risk Equations for Complications Of type 2 Diabetes (RECODe). Methods To develop and validate these risk equations, we used data from the Action to Control Cardiovascular Risk in Diabetes study (ACCORD, n = 9635; 2001-09) and validated the equations for microvascular events using data from the Diabetes Prevention Program Outcomes Study (DPPOS, n = 1018; 1996-2001), and for cardiovascular events using data from the Action for Health in Diabetes (Look AHEAD, n = 4760; 2001-12). Microvascular outcomes were nephropathy, retinopathy, and neuropathy. Cardiovascular outcomes were myocardial infarction, stroke, congestive heart failure, and cardiovascular mortality. We also included all-cause mortality as an outcome. We used a cross-validating machine learning method to select predictor variables from demographic characteristics, clinical variables, comorbidities, medications, and biomarkers into Cox proportional hazards models for each outcome. The new equations were compared to older risk equations by assessing model discrimination, calibration, and the net reclassification index. Findings All equations had moderate internal and external discrimination (C-statistics 0.55-0.84 internally, 0.57-0.79 externally) and high internal and external calibration (slopes 0.71-1.31 between observed and estimated risk). Our equations had better discrimination and calibration than the UK Prospective Diabetes Study Outcomes Model 2 (for microvascular and cardiovascular outcomes, C-statistics 0.54-0.62, slopes 0.06-1.12) and the American College of Cardiology/American Heart Association Pooled Cohort Equations (for fatal or non-fatal myocardial infarction or stroke, C-statistics 0.61-0.66, slopes 0.30-0.39). Interpretation RECODe might improve estimation of risk of complications for patients with type 2 diabetes.
引用
收藏
页码:788 / 798
页数:11
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