Trajectories of Non-HDL Cholesterol Across Midlife Implications for Cardiovascular Prevention

被引:81
作者
Pencina, Karol M. [1 ]
Thanassoulis, George [2 ]
Wilkins, John T. [3 ]
Vasan, Ramachandran S. [4 ,5 ,6 ]
Navar, Ann Marie [7 ]
Peterson, Eric D. [8 ]
Pencina, Michael J. [9 ]
Sniderman, Allan D. [10 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Sect Mens Hlth Aging & Metab, Boston, MA 02115 USA
[2] McGill Univ, Div Expt Med, Dept Med, Montreal, PQ, Canada
[3] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[4] Boston Univ, Sch Med, Dept Med, Framingham Heart Study,Sect Prevent Med, Boston, MA 02118 USA
[5] Boston Univ, Sch Med, Dept Med, Sect Cardiol, Boston, MA 02118 USA
[6] Boston Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[7] Duke Clin Res Inst, Durham, NC USA
[8] Duke Univ, Sch Med, Dept Med, Div Cardiol, Durham, NC 27706 USA
[9] Duke Univ, Sch Med, Duke Clin Res Inst, Durham, NC USA
[10] McGill Univ, Dept Med, Div Expt Med, Montreal, PQ, Canada
基金
美国国家卫生研究院;
关键词
cardiovascular disease prevention; lipids; non-HDL cholesterol; ANALYZING DEVELOPMENTAL TRAJECTORIES; APOLIPOPROTEIN-B; RISK; DISEASE; ASSOCIATION; DISCORDANCE; THERAPY; NUMBER;
D O I
10.1016/j.jacc.2019.04.047
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Extended elevations of non-high-density lipoprotein cholesterol (non-HDL-C) across a lifespan are associated with increased risk of cardiovascular disease (CVD). However, optimal testing intervals to identify individuals with high lipid-related CVD risk are unknown. OBJECTIVES This study determined the extent to which lipid levels in young adulthood predict future lipid trajectories and associated long-term CVD risk. METHODS A sample of 2,516 Framingham Offspring study participants 25 to 40 years of age free of CVD and diabetes had their non-HDL-C progression modeled over 8 study examinations (mean follow-up 32.6 years) using group-based methods. CVD risk based on 25 to 30 years of follow-up was evaluated using Kaplan-Meier analyses for those with mean non-HDL-C >= 160 mg/dl ("high") and < 130 mg/dl ("low") at the first 2 examinations. Levels of non-HDL-C for participants on lipid treatment were adjusted by nonparametric algorithm. RESULTS The trajectories of the lipid levels were generally stable over the 30-year life course; mean non-HDL-C measured in young adulthood were highly predictive of levels later in life. Individuals could be reliably assigned to high and low non-HDL-C groups based on 2 measurements collected between 25 to 40 years of age. Overall, 80% of those with non-HDL-C >= 160 mg/dl at the first 2 exams remained in the high group on subsequent 25-year testing, whereas 88% of those with non-HDL-C < 130 mg/dl remained below 160 mg/dl. Those with high non-HDL-C in young adulthood had a 22.6% risk of CVD in the next 25 years as compared with a 6.4% risk in those with low non-HDL-C. CONCLUSIONS Most adults with elevated non-HDL-C early in life continue to have high non-HDL-C over their life course, leading to significantly increased risk of CVD. The results demonstrate that early lipid monitoring before 40 years of age would identify a majority of those with a high likelihood for lifetime elevated lipid levels who also have a high long-term risk for CVD. This information could facilitate informed patient-provider discussion about the potential benefits of preventive lipid-lowering efforts during the early midlife period. (C) 2019 by the American College of Cardiology Foundation.
引用
收藏
页码:70 / 79
页数:10
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