Risk factors and prediction models for incident heart failure with reduced and preserved ejection fraction

被引:19
作者
Gaziano, Liam [1 ,2 ]
Cho, Kelly [1 ,3 ]
Djousse, Luc [1 ,3 ]
Schubert, Petra [1 ]
Galloway, Ashley [1 ]
Ho, Yuk-Lam [1 ]
Kurgansky, Katherine [1 ]
Gagnon, David R. [1 ,4 ]
Russo, John P. [1 ,5 ]
Di Angelantonio, Emanuele [2 ]
Wood, Angela M. [2 ]
Danesh, John [2 ]
Gaziano, John Michael [1 ,3 ]
Butterworth, Adam S. [2 ]
Wilson, Peter W. F. [6 ,7 ]
Joseph, Jacob [1 ,8 ]
机构
[1] VA Boston Healthcare Syst, Cardiol Sect, Massachusetts Vet Epidemiol Res & Informat Ctr MA, 1400 VFW Pkwy, Boston, MA 02132 USA
[2] Univ Cambridge, Dept Publ Hlth & Primary Care, BHF Cardiovasc Epidemiol Unit, Cambridge, England
[3] Harvard Med Sch, Brigham & Womens Hosp, Div Aging, Dept Med, Boston, MA USA
[4] Boston Univ, Dept Biostat, Sch Publ Hlth, Boston, MA USA
[5] Landmark Coll, Putney, VT USA
[6] Atlanta VA Med Ctr, Decatur, GA USA
[7] Emory Univ, Div Cardiovasc Dis, Dept Med, Sch Med, Atlanta, GA USA
[8] Harvard Med Sch, Brigham & Womens Hosp, Div Cardiovasc Med, Dept Med, Boston, MA USA
基金
英国医学研究理事会;
关键词
Risk prediction; Heart failure; Heart failure with reduced ejection fraction; Heart failure with preserved ejection fraction; Electronic health records; LEFT-VENTRICULAR HYPERTROPHY; COHORT; SURVIVAL; HYPERTENSION; ASSOCIATION; DYSFUNCTION; POPULATION; INHIBITION; PREVENTION; PHENOTYPES;
D O I
10.1002/ehf2.13429
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims This study aims to develop the first race-specific and sex-specific risk prediction models for heart failure with preserved (HFpEF) and reduced ejection fraction (HFrEF). Methods and results We created a cohort of 1.8 million individuals who had an outpatient clinic visit between 2002 and 2007 within the Veterans Affairs (VA) Healthcare System and obtained information on HFpEF, HFrEF, and several risk factors from electronic health records (EHR). Variables were selected for the risk prediction models in a 'derivation cohort' that consisted of individuals with baseline date in 2002, 2003, or 2004 using a forward stepwise selection based on a change in C-index threshold. Discrimination and calibration were assessed in the remaining participants (internal 'validation cohort'). A total of 66 831 individuals developed HFpEF, and 92 233 developed HFrEF (52 679 and 71 463 in the derivation cohort) over a median of 11.1 years of follow-up. The HFpEF risk prediction model included age, diabetes, BMI, COPD, previous MI, anti-hypertensive treatment, SBP, smoking status, atrial fibrillation, and estimated glomerular filtration rate (eGFR), while the HFrEF model additionally included previous CAD. For the HFpEF model, C-indices were 0.74 (SE = 0.002) for white men, 0.76 (0.005) for black men, 0.79 (0.015) for white women, and 0.77 (0.026) for black women, compared with 0.72 (0.002), 0.72 (0.004), 0.77 (0.017), and 0.75 (0.028), respectively, for the HFrEF model. These risk prediction models were generally well calibrated in each race-specific and sex-specific stratum of the validation cohort. Conclusions Our race-specific and sex-specific risk prediction models, which used easily obtainable clinical variables, can be a useful tool to implement preventive strategies or subtype-specific prevention trials in the nine million users of the VA healthcare system and the general population after external validation.
引用
收藏
页码:4893 / 4903
页数:11
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