Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, USA.
Cardiovascular Division, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.
J Clin Lipidol. 2020 Jul-Aug;14(4):531-541. doi: 10.1016/j.jacl.2020.06.005. Epub 2020 Jun 10.
Fasting free fatty acid (FFA) levels may be associated with cardiovascular disease (CVD) and mortality, but research among generally healthy adults, females, and racially/ethnically diverse populations is lacking.
The primary aim of this project was to investigate prospective associations between fasting FFAs and coronary heart disease (CHD) and CVD incidence and CVD-specific and all-cause mortality in a generally healthy age, sex, and racially/ethnically heterogeneous population.
This study was conducted in the Multi-Ethnic Study of Atherosclerosis cohort using baseline (2000-2002) fasting FFAs and outcome data through 2015 (N = 6678). Cox proportional hazards regression was used to calculate hazard ratios for associations between FFAs and CHD, CVD, CVD-specific mortality, and all-cause mortality. Interactions by age, sex, race/ethnicity, and metabolic syndrome were evaluated by stratification and cross-product terms. A secondary analysis was conducted to evaluate associations between FFAs, and inflammatory and endothelial activation biomarkers were evaluated using linear regression (analytic N range: 964-6662).
FFA levels were not associated with CHD or CVD incidence. Higher FFAs were associated with CVD-specific and all-cause mortality, but associations were attenuated in fully adjusted models with a borderline significant association remaining only for all-cause mortality (fully adjusted, per standard deviation increase hazard ratio = 1.07, 95% confidence interval: 1.00-1.14). Associations did not differ by age, sex, race/ethnicity, or metabolic syndrome.
Fasting FFAs were not associated with CHD, CVD, or CVD-specific mortality and were modestly associated with all-cause mortality, regardless of age, sex, race/ethnicity, or metabolic syndrome status.
空腹游离脂肪酸(FFA)水平可能与心血管疾病(CVD)和死亡率有关,但在一般健康成年人、女性以及不同种族/民族人群中的研究还很缺乏。
本项目的主要目的是在一个一般健康、年龄、性别和种族/民族多样化的人群中,调查空腹 FFA 与冠心病(CHD)和 CVD 发病以及 CVD 特异性和全因死亡率之间的前瞻性关联。
本研究在动脉粥样硬化多民族研究队列中进行,使用基线(2000-2002 年)空腹 FFA 和 2015 年的结局数据(N=6678)。使用 Cox 比例风险回归计算 FFA 与 CHD、CVD、CVD 特异性死亡率和全因死亡率之间关联的风险比。通过分层和交叉乘积项评估年龄、性别、种族/民族和代谢综合征的交互作用。进行了二次分析,以评估 FFA 与炎症和内皮激活生物标志物之间的关联,使用线性回归(分析 N 范围:964-6662)。
FFA 水平与 CHD 或 CVD 发病率无关。较高的 FFA 与 CVD 特异性和全因死亡率相关,但在完全调整模型中,关联减弱,仅全因死亡率存在边缘显著关联(完全调整后,每标准差增加的风险比为 1.07,95%置信区间:1.00-1.14)。关联在年龄、性别、种族/民族或代谢综合征方面没有差异。
空腹 FFA 与 CHD、CVD 或 CVD 特异性死亡率无关,与全因死亡率有适度关联,无论年龄、性别、种族/民族或代谢综合征状态如何。