Center for Lipid Metabolomics, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Division of Hospital Internal Medicine, Mayo Clinic, Rochester, Minnesota.
JAMA Cardiol. 2021 Apr 1;6(4):437-447. doi: 10.1001/jamacardio.2020.7073.
Risk profiles for premature coronary heart disease (CHD) are unclear.
To examine baseline risk profiles for incident CHD in women by age at onset.
DESIGN, SETTING, AND PARTICIPANTS: A prospective cohort of US female health professionals participating in the Women's Health Study was conducted; median follow-up was 21.4 years. Participants included 28 024 women aged 45 years or older without known cardiovascular disease. Baseline profiles were obtained from April 30, 1993, to January 24, 1996, and analyses were conducted from October 1, 2017, to October 1, 2020.
More than 50 clinical, lipid, inflammatory, and metabolic risk factors and biomarkers.
Four age groups were examined (<55, 55 to <65, 65 to <75, and ≥75 years) for CHD onset, and adjusted hazard ratios (aHRs) were calculated using stratified Cox proportional hazard regression models with age as the time scale and adjusting for clinical factors. Women contributed to different age groups over time.
Of the clinical factors in the women, diabetes had the highest aHR for CHD onset at any age, ranging from 10.71 (95% CI, 5.57-20.60) at CHD onset in those younger than 55 years to 3.47 (95% CI, 2.47-4.87) at CHD onset in those 75 years or older. Risks that were also noted for CHD onset in participants younger than 55 years included metabolic syndrome (aHR, 6.09; 95% CI, 3.60-10.29), hypertension (aHR, 4.58; 95% CI, 2.76-7.60), obesity (aHR, 4.33; 95% CI, 2.31-8.11), and smoking (aHR, 3.92; 95% CI, 2.32-6.63). Myocardial infarction in a parent before age 60 years was associated with 1.5- to 2-fold risk of CHD in participants up to age 75 years. From approximately 50 biomarkers, lipoprotein insulin resistance had the highest standardized aHR: 6.40 (95% CI, 3.14-13.06) for CHD onset in women younger than 55 years, attenuating with age. In comparison, weaker but significant associations with CHD in women younger than 55 years were noted (per SD increment) for low-density lipoprotein cholesterol (aHR, 1.38; 95% CI, 1.10-1.74), non-high-density lipoprotein cholesterol (aHR, 1.67; 95% CI, 1.36-2.04), apolipoprotein B (aHR, 1.89; 95% CI, 1.52-2.35), triglycerides (aHR, 2.14; 95% CI, 1.72-2.67), and inflammatory biomarkers (1.2- to 1.8-fold)-all attenuating with age. Some biomarkers had similar CHD age associations (eg, physical inactivity, lipoprotein[a], total high-density lipoprotein particles), while a few had no association with CHD onset at any age. Most risk factors and biomarkers had associations that attenuated with increasing age at onset.
In this cohort study, diabetes and insulin resistance, in addition to hypertension, obesity, and smoking, appeared to be the strongest risk factors for premature onset of CHD. Most risk factors had attenuated relative rates at older ages.
重要性:早发性冠心病(CHD)的风险特征尚不清楚。
目的:通过发病年龄来研究女性发生 CHD 的基线风险特征。
设计、地点和参与者:一项美国女性健康专业人员参加的妇女健康研究的前瞻性队列研究;中位随访时间为 21.4 年。参与者包括 28024 名年龄在 45 岁或以上且无心血管疾病的女性。基线特征于 1993 年 4 月 30 日至 1996 年 1 月 24 日获取,分析于 2017 年 10 月 1 日至 2020 年 10 月 1 日进行。
暴露:超过 50 种临床、血脂、炎症和代谢风险因素及生物标志物。
主要结果和措施:共观察了 4 个年龄组(<55 岁、55 岁至<65 岁、65 岁至<75 岁和≥75 岁)的 CHD 发病情况,并使用分层 Cox 比例风险回归模型计算了调整后的危险比(aHR),该模型以年龄为时间尺度,并调整了临床因素。女性在不同年龄组中的贡献随着时间的推移而不同。
结果:在女性的临床因素中,糖尿病的 aHR 最高,与任何年龄的 CHD 发病相关,从 55 岁以下 CHD 发病的 10.71(95%CI,5.57-20.60)到 75 岁及以上 CHD 发病的 3.47(95%CI,2.47-4.87)。在 55 岁以下的参与者中,CHD 发病的其他风险因素还包括代谢综合征(aHR,6.09;95%CI,3.60-10.29)、高血压(aHR,4.58;95%CI,2.76-7.60)、肥胖(aHR,4.33;95%CI,2.31-8.11)和吸烟(aHR,3.92;95%CI,2.32-6.63)。父母在 60 岁前发生心肌梗死与 75 岁以下参与者的 CHD 发病风险增加 1.5-2 倍相关。在大约 50 种生物标志物中,脂蛋白胰岛素抵抗的标准化 aHR 最高:55 岁以下女性 CHD 发病的 aHR 为 6.40(95%CI,3.14-13.06),随着年龄的增长而减弱。相比之下,在 55 岁以下的女性中,与 CHD 发病相关的但较弱的生物标志物包括低密度脂蛋白胆固醇(每 SD 增加,aHR,1.38;95%CI,1.10-1.74)、非高密度脂蛋白胆固醇(aHR,1.67;95%CI,1.36-2.04)、载脂蛋白 B(aHR,1.89;95%CI,1.52-2.35)、甘油三酯(aHR,2.14;95%CI,1.72-2.67)和炎症生物标志物(1.2-1.8 倍),所有这些生物标志物均随着年龄的增长而减弱。一些生物标志物与 CHD 发病年龄相关(如,体力活动不足、脂蛋白[a]、总高密度脂蛋白颗粒),而一些生物标志物与任何年龄的 CHD 发病均无关。大多数风险因素和生物标志物的关联随着发病年龄的增加而减弱。
结论和相关性:在这项队列研究中,除了高血压、肥胖和吸烟之外,糖尿病和胰岛素抵抗似乎也是早发性 CHD 的最强危险因素。大多数危险因素在年龄较大时的相对风险较低。