Genetic, sociodemographic, lifestyle, and clinical risk factors of recurrent coronary artery disease events: a population-based cohort study

被引:40
作者
Cho, So Mi Jemma [1 ,2 ,3 ,4 ]
Koyama, Satoshi [1 ,2 ,3 ]
Honigberg, Michael C. [1 ,2 ,3 ,5 ,6 ]
Surakka, Ida [1 ,7 ]
Haidermota, Sara [1 ,2 ,3 ]
Ganesh, Shriienidhie [1 ,2 ,3 ]
Patel, Aniruddh P. [1 ,2 ,3 ,5 ,6 ]
Bhattacharya, Romit [1 ,2 ,3 ,5 ,6 ]
Lee, Hokyou [8 ]
Kim, Hyeon Chang [4 ,8 ,9 ]
Natarajan, Pradeep [1 ,2 ,3 ,5 ,6 ]
机构
[1] Broad Inst MIT & Harvard, Program Med & Populat Genet & Cardiovasc Dis Initi, 415 Main St, Cambridge, MA 02142 USA
[2] Massachusetts Gen Hosp, Cardiovasc Res Ctr, 185 Cambridge St, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Ctr Genom Med, 185 Cambridge St, Boston, MA 02114 USA
[4] Yonsei Univ, Integrat Res Ctr Cerebrovasc & Cardiovasc Dis, Coll Med, 50-1 Yonsei ro, Seoul 03722, South Korea
[5] Massachusetts Gen Hosp, Dept Med, Cardiol Div, 55 Fruit St, Boston, MA 02114 USA
[6] Harvard Med Sch, Dept Med, 25 Shattuck St, Boston, MA 02114 USA
[7] Univ Michigan, Dept Internal Med, Div Cardiol, 1500 E Med Ctr Dr, Ann Arbor, MI 48109 USA
[8] Yonsei Univ, Dept Prevent Med, Coll Med, 50-1 Yonsei ro, Seoul 03722, South Korea
[9] Yonsei Univ Hlth Syst, Inst Innovat Digital Healthcare, 50-1 Yonsei ro, Seoul 03722, South Korea
关键词
Secondary prevention; Coronary artery disease; Risk prediction; Preventive cardiology; Epidemiology; CARDIOVASCULAR-DISEASE; MYOCARDIAL-INFARCTION; CHANGING LANDSCAPE; HEART-DISEASE; ASSOCIATION; THERAPY; METAANALYSIS; PREDICTION; GUIDELINE; EVOLUTION;
D O I
10.1093/eurheartj/ehad380
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Complications of coronary artery disease (CAD) represent the leading cause of death among adults globally. This study examined the associations and clinical utilities of genetic, sociodemographic, lifestyle, and clinical risk factors on CAD recurrence. Methods and results Data were from 7024 UK Biobank middle-aged adults with established CAD at enrolment. Cox proportional hazards regressions modelled associations of age at enrolment, age at first CAD diagnosis, sex, cigarette smoking, physical activity, diet, sleep, Townsend Deprivation Index, body mass index, blood pressure, blood lipids, glucose, lipoprotein(a), C reactive protein, estimated glomerular filtration rate (eGFR), statin prescription, and CAD polygenic risk score (PRS) with first post-enrolment CAD recurrence. Over a median [interquartile range] follow-up of 11.6 [7.2-12.7] years, 2003 (28.5%) recurrent CAD events occurred. The hazard ratio (95% confidence interval [CI]) for CAD recurrence was the most pronounced with current smoking (1.35, 1.13-1.61) and per standard deviation increase in age at first CAD (0.74, 0.67-0.82). Additionally, age at enrolment, CAD PRS, C-reactive protein, lipoprotein(a), glucose, low-density lipoprotein cholesterol, deprivation, sleep quality, eGFR, and high-density lipoprotein (HDL) cholesterol also significantly associated with recurrence risk. Based on C indices (95% CI), the strongest predictors were CAD PRS (0.58, 0.57-0.59), HDL cholesterol (0.57, 0.57-0.58), and age at initial CAD event (0.57, 0.56-0.57). In addition to traditional risk factors, a comprehensive model improved the C index from 0.644 (0.632-0.654) to 0.676 (0.667-0.686). Conclusion Sociodemographic, clinical, and laboratory factors are each associated with CAD recurrence with genetic risk, age at first CAD event, and HDL cholesterol concentration explaining the most.
引用
收藏
页码:3456 / 3465
页数:12
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